Crystallography Open Database

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1553260 CIFC21 H25 F2 N3 O2P 21 21 217.5165; 8.0959; 24.661
90; 90; 90
1500.7Das, Pronay; Babbar, Palak; Malhotra, Nipun; Sharma, Manmohan; Jachak, Goraknath R.; Gonnade, Rajesh G.; Shanmugam, Dhanasekaran; Harlos, Karl; Yogavel, Manickam; Sharma, Amit; Reddy, D. Srinivasa
Specific Stereoisomeric Conformations Determine the Drug Potency of Cladosporin Scaffold against Malarial Parasite.
Journal of medicinal chemistry, 2018, 61, 5664-5678
1553261 CIFC27 H32 N2 O4P 1 21/c 19.41991; 10.1144; 23.7285
90; 91.6653; 90
2259.82Zhang, Xiao-Ru; Wang, Hao-Wen; Tang, Wen-Lin; Zhang, Yu; Yang, Hui; Hu, De-Xuan; Ravji, Azhar; Marchand, Christophe; Kiselev, Evgeny; Ofori-Atta, Kwabena; Agama, Keli; Pommier, Yves; An, Lin-Kun
Discovery, Synthesis, and Evaluation of Oxynitidine Derivatives as Dual Inhibitors of DNA Topoisomerase IB (TOP1) and Tyrosyl-DNA Phosphodiesterase 1 (TDP1), and Potential Antitumor Agents.
Journal of medicinal chemistry, 2018, 61, 9908-9930
1553262 CIFC29.2 H31.8 Cl Ir N5 O0.2P -19.804; 15.8991; 18.4457
82.7271; 86.7456; 72.239
2715.65Chen, Feng; Moat, John; McFeely, Daniel; Clarkson, Guy; Hands-Portman, Ian J; Furner-Pardoe, Jessica P; Harrison, Freya; Dowson, Christopher G.; Sadler, Peter J.
Biguanide Iridium(III) Complexes with Potent Antimicrobial Activity.
Journal of medicinal chemistry, 2018, 61, 7330-7344
1553263 CIFC18.75 H26 Cl Ir N5 O0.75P b c a11.78544; 14.43434; 23.04719
90; 90; 90
3920.67Chen, Feng; Moat, John; McFeely, Daniel; Clarkson, Guy; Hands-Portman, Ian J; Furner-Pardoe, Jessica P; Harrison, Freya; Dowson, Christopher G.; Sadler, Peter J.
Biguanide Iridium(III) Complexes with Potent Antimicrobial Activity.
Journal of medicinal chemistry, 2018, 61, 7330-7344
1553264 CIFC26 H23 N3 O3P -17.738; 10.534; 14.044
70.163; 86.367; 81.901
1065.9Wu, Qiong; Zheng, Kangdi; Huang, Xiaoting; Li, Li; Mei, Wenjie
Tanshinone-IIA-Based Analogues of Imidazole Alkaloid Act as Potent Inhibitors To Block Breast Cancer Invasion and Metastasis in Vivo.
Journal of medicinal chemistry, 2018, 61, 10488-10501
1553265 CIFC27 H26 N2 O2P 1 21/c 112.27; 21.5852; 8.2015
90; 99.774; 90
2140.64Wu, Qiong; Zheng, Kangdi; Huang, Xiaoting; Li, Li; Mei, Wenjie
Tanshinone-IIA-Based Analogues of Imidazole Alkaloid Act as Potent Inhibitors To Block Breast Cancer Invasion and Metastasis in Vivo.
Journal of medicinal chemistry, 2018, 61, 10488-10501
1553266 CIFC26 H24 N2 O2P 1 21/c 110.2122; 16.083; 12.5447
90; 104.737; 90
1992.6Wu, Qiong; Zheng, Kangdi; Huang, Xiaoting; Li, Li; Mei, Wenjie
Tanshinone-IIA-Based Analogues of Imidazole Alkaloid Act as Potent Inhibitors To Block Breast Cancer Invasion and Metastasis in Vivo.
Journal of medicinal chemistry, 2018, 61, 10488-10501
1553267 CIFC12 H22 Cl Cu N5 O4 SP -19.2626; 9.5087; 11.0617
89.565; 76.519; 67.742
873.29Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553268 CIFC15 H23 Cl Cu N6 O2 SP 1 21/c 19.3959; 19.8889; 10.9744
90; 108.366; 90
1946.37Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553269 CIFC13 H18 Cl Cu N5 O SC 1 2/c 115.7566; 14.2967; 14.2703
90; 92.971; 90
3210.3Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553270 CIFC16 H23 N5 O2 SP 1 21/c 113.3622; 5.8899; 21.414
90; 91.631; 90
1684.6Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553271 CIFC12 H17 N5 O SP 1 21/c 111.544; 13.204; 10.086
90; 112.081; 90
1424.6Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553272 CIFC18 H21 N5 O SP 1 21/n 17.1287; 15.0536; 16.4704
90; 97.81; 90
1751.09Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553273 CIFC48.75 H69 Cl3 Cu3 N15 O3.75 S3P 1 21/n 124.702; 9.1959; 25.064
90; 100.971; 90
5589.4Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553274 CIFC14 H21 N5 O SP 1 21/c 16.1236; 7.95; 30.956
90; 92.419; 90
1505.68Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553275 CIFC13 H19 N5 O SP 1 21/c 122.7776; 6.8585; 9.88
90; 98.889; 90
1524.92Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553276 CIFC49.75 H73 Cl3 Cu3 N15 O7.75 S3P 1 21/n 122.2413; 8.3324; 31.9121
90; 90.5654; 90
5913.8Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553277 CIFC19 H24 Cl Cu N5 O2 SP 1 21/c 116.5043; 17.7857; 7.1311
90; 96.241; 90
2080.9Ohui, Kateryna; Afanasenko, Eleonora; Bacher, Felix; Ting, Rachel Lim Xue; Zafar, Ayesha; Blanco-Cabra, Núria; Torrents, Eduard; Dömötör, Orsolya; May, Nóra V; Darvasiova, Denisa; Enyedy, Éva A; Popović-Bijelić, Ana; Reynisson, Jóhannes; Rapta, Peter; Babak, Maria V.; Pastorin, Giorgia; Arion, Vladimir B.
New Water-Soluble Copper(II) Complexes with Morpholine-Thiosemicarbazone Hybrids: Insights into the Anticancer and Antibacterial Mode of Action.
Journal of medicinal chemistry, 2019, 62, 512-530
1553278 CIFC9 H7 Cl N6P 21 21 215.436; 9.003; 21.664
90; 90; 90
1060.2Tokarenko, Anna; Lišková, Barbora; Smoleń, Sabina; Táborská, Natálie; Tichý, Michal; Gurská, Soňa; Perlíková, Pavla; Frydrych, Ivo; Tloušt'ová, Eva; Znojek, Pawel; Mertlíková-Kaiserová, Helena; Poštová Slavětínská, Lenka; Pohl, Radek; Klepetářová, Blanka; Khalid, Noor-Ul-Ain; Wenren, Yiqian; Laposa, Rebecca R.; Džubák, Petr; Hajdúch, Marián; Hocek, Michal
Synthesis and Cytotoxic and Antiviral Profiling of Pyrrolo- and Furo-Fused 7-Deazapurine Ribonucleosides.
Journal of medicinal chemistry, 2018, 61, 9347-9359
1553279 CIFC9 H7 Cl N4P 1 21/n 18.2465; 6.6263; 16.392
90; 97.969; 90
887.07Tokarenko, Anna; Lišková, Barbora; Smoleń, Sabina; Táborská, Natálie; Tichý, Michal; Gurská, Soňa; Perlíková, Pavla; Frydrych, Ivo; Tloušt'ová, Eva; Znojek, Pawel; Mertlíková-Kaiserová, Helena; Poštová Slavětínská, Lenka; Pohl, Radek; Klepetářová, Blanka; Khalid, Noor-Ul-Ain; Wenren, Yiqian; Laposa, Rebecca R.; Džubák, Petr; Hajdúch, Marián; Hocek, Michal
Synthesis and Cytotoxic and Antiviral Profiling of Pyrrolo- and Furo-Fused 7-Deazapurine Ribonucleosides.
Journal of medicinal chemistry, 2018, 61, 9347-9359
1553280 CIFC34 H54 O4P 21 21 219.3781; 12.6568; 27.0482
90; 90; 90
3210.53Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553281 CIFC69 H92 O13C 1 2 118.0066; 13.5854; 13.2739
90; 93.898; 90
3239.64Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553282 CIFC36 H54 O5P 1 21 19.3216; 13.2025; 13.8291
90; 107.968; 90
1618.92Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553283 CIFC30 H36 O4P 1 21 110.7509; 7.7655; 14.8907
90; 99.69; 90
1225.43Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553284 CIFC30 H44 O5P 21 21 2110.0575; 16.0634; 17.39
90; 90; 90
2809.49Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553285 CIFC16 H24.6667 N2 O1.3333P 21 21 219.7135; 13.9213; 31.7069
90; 90; 90
4287.6Cao, Ming-Ming; Zhang, Yu; Huang, Sheng-Dian; Di, Ying-Tong; Peng, Zong-Gen; Jiang, Jian-Dong; Yuan, Chun-Mao; Chen, Duo-Zhi; Li, Shun-Lin; He, Hong-Ping; Hao, Xiao-Jiang
Alkaloids with Different Carbon Units from Myrioneuron faberi.
Journal of natural products, 2015, 78, 2609-2616
1553286 CIFC15 H26 N2P 1 21 19.1535; 5.1702; 14.568
90; 106.495; 90
661.06Cao, Ming-Ming; Zhang, Yu; Huang, Sheng-Dian; Di, Ying-Tong; Peng, Zong-Gen; Jiang, Jian-Dong; Yuan, Chun-Mao; Chen, Duo-Zhi; Li, Shun-Lin; He, Hong-Ping; Hao, Xiao-Jiang
Alkaloids with Different Carbon Units from Myrioneuron faberi.
Journal of natural products, 2015, 78, 2609-2616
1553287 CIFC15 H24 N2 OP -18.8466; 9.1188; 9.5971
95.094; 112.717; 112.004
636.97Cao, Ming-Ming; Zhang, Yu; Huang, Sheng-Dian; Di, Ying-Tong; Peng, Zong-Gen; Jiang, Jian-Dong; Yuan, Chun-Mao; Chen, Duo-Zhi; Li, Shun-Lin; He, Hong-Ping; Hao, Xiao-Jiang
Alkaloids with Different Carbon Units from Myrioneuron faberi.
Journal of natural products, 2015, 78, 2609-2616
1553288 CIFC15 H22 O2P 21 21 215.8324; 12.9306; 17.55
90; 90; 90
1323.6Matsuo, Yukiko; Maeda, Saori; Ohba, Chika; Fukaya, Haruhiko; Mimaki, Yoshihiro
Vetiverianines A, B, and C: Sesquiterpenoids from Vetiveria zizanioides Roots.
Journal of natural products, 2016, 79, 2175-2180
1553289 CIFC15 H27 O2.5P 21 21 216.242; 16.329; 28.076
90; 90; 90
2861.7Matsuo, Yukiko; Maeda, Saori; Ohba, Chika; Fukaya, Haruhiko; Mimaki, Yoshihiro
Vetiverianines A, B, and C: Sesquiterpenoids from Vetiveria zizanioides Roots.
Journal of natural products, 2016, 79, 2175-2180
1553290 CIFC15 H24 O2P 21 21 215.6076; 7.3152; 32.2
90; 90; 90
1320.9Matsuo, Yukiko; Maeda, Saori; Ohba, Chika; Fukaya, Haruhiko; Mimaki, Yoshihiro
Vetiverianines A, B, and C: Sesquiterpenoids from Vetiveria zizanioides Roots.
Journal of natural products, 2016, 79, 2175-2180
1553291 CIFC23 H26 O7P 21 21 219.1399; 11.2214; 19.328
90; 90; 90
1982.33Abdissa, Negera; Pan, Fangfang; Gruhonjic, Amra; Gräfenstein, Jürgen; Fitzpatrick, Paul A.; Landberg, Göran; Rissanen, Kari; Yenesew, Abiy; Erdélyi, Máté
Naphthalene Derivatives from the Roots of Pentas parvifolia and Pentas bussei.
Journal of natural products, 2016, 79, 2181-2187
1553292 CIFC24 H28 O7P 21 21 215.20049; 18.36541; 22.63281
90; 90; 90
2161.64Abdissa, Negera; Pan, Fangfang; Gruhonjic, Amra; Gräfenstein, Jürgen; Fitzpatrick, Paul A.; Landberg, Göran; Rissanen, Kari; Yenesew, Abiy; Erdélyi, Máté
Naphthalene Derivatives from the Roots of Pentas parvifolia and Pentas bussei.
Journal of natural products, 2016, 79, 2181-2187
1553293 CIFC13 H12 N2 O3P 21 21 216.5201; 7.2318; 24.7168
90; 90; 90
1165.45Zhou, Haibo; Li, Liyuan; Wu, Chongming; Kurtán, Tibor; Mándi, Attila; Liu, Yankai; Gu, Qianqun; Zhu, Tianjiao; Guo, Peng; Li, Dehai
Penipyridones A-F, Pyridone Alkaloids from Penicillium funiculosum.
Journal of natural products, 2016, 79, 1783-1790
1553294 CIFC45 H63 N O7P 16.3429; 7.2295; 22.835
86.897; 87.866; 68.166
970.42Li, Jin-Long; Wu, Lei; Wu, Jian; Feng, Hong-Xuan; Wang, Hong-Min; Fu, Yan; Zhang, Ru-Jun; Zhang, Hai-Yan; Zhao, Wei-Min
Caffeoyl Triterpenoid Esters as Potential Anti-ischemic Stroke Agents from Celastrus orbiculatus.
Journal of natural products, 2016, 79, 2774-2779
1553295 CIFC10 H13 N O4P 21 21 217.33508; 7.7336; 16.8499
90; 90; 90
955.84Zeng, Yao-Bo; Liu, Xiao-Ling; Zhang, Yi; Li, Chuang-Jun; Zhang, Dong-Ming; Peng, Yao-Zong; Zhou, Xing; Du, Hong-Fei; Tan, Chun-Bing; Zhang, Yu-Yu; Yang, Da-Jian
Cantharimide and Its Derivatives from the Blister Beetle Mylabris phalerata Palla.
Journal of natural products, 2016, 79, 2032-2038
1553296 CIFC9 H11 N O3P 21 21 215.376; 11.9366; 13.1122
90; 90; 90
841.43Zeng, Yao-Bo; Liu, Xiao-Ling; Zhang, Yi; Li, Chuang-Jun; Zhang, Dong-Ming; Peng, Yao-Zong; Zhou, Xing; Du, Hong-Fei; Tan, Chun-Bing; Zhang, Yu-Yu; Yang, Da-Jian
Cantharimide and Its Derivatives from the Blister Beetle Mylabris phalerata Palla.
Journal of natural products, 2016, 79, 2032-2038
1553297 CIFC37 H26 N2 O7P 1 21/c 18.2263; 19.2406; 16.9322
90; 93.261; 90
2675.67Shono, Takumi; Ishikawa, Naoki; Toume, Kazufumi; Arai, Midori A.; Masu, Hyuma; Koyano, Takashi; Kowithayakorn, Thaworn; Ishibashi, Masami
Cerasoidine, a Bis-aporphine Alkaloid Isolated from Polyalthia cerasoides during Screening for Wnt Signal Inhibitors.
Journal of natural products, 2016, 79, 2083-2088
1553298 CIFC14 H19 Br O2P 21 21 217.3316; 9.7804; 17.8769
90; 90; 90
1281.88Chen, Jia-Yu; Huang, Chiung-Yao; Lin, Yun-Sheng; Hwang, Tsong-Long; Wang, Wei-Lung; Chiou, Shu-Fen; Sheu, Jyh-Horng
Halogenated Sesquiterpenoids from the Red Alga Laurencia tristicha Collected in Taiwan.
Journal of natural products, 2016, 79, 2315-2323
1553299 CIFC14 H22 O6P 16.3082; 7.5108; 8.11
88.911; 85.044; 77.888
374.29Liu, Shuai; Dai, Haofu; Makhloufi, Gamall; Heering, Christian; Janiak, Christoph; Hartmann, Rudolf; Mándi, Attila; Kurtán, Tibor; Müller, Werner E G; Kassack, Matthias U.; Lin, Wenhan; Liu, Zhen; Proksch, Peter
Cytotoxic 14-Membered Macrolides from a Mangrove-Derived Endophytic Fungus, Pestalotiopsis microspora.
Journal of natural products, 2016, 79, 2332-2340
1553300 CIFC14 H24 O4P 21 21 2136.533; 4.9693; 7.6479
90; 90; 90
1388.4Liu, Shuai; Dai, Haofu; Makhloufi, Gamall; Heering, Christian; Janiak, Christoph; Hartmann, Rudolf; Mándi, Attila; Kurtán, Tibor; Müller, Werner E G; Kassack, Matthias U.; Lin, Wenhan; Liu, Zhen; Proksch, Peter
Cytotoxic 14-Membered Macrolides from a Mangrove-Derived Endophytic Fungus, Pestalotiopsis microspora.
Journal of natural products, 2016, 79, 2332-2340
1553301 CIFC14 H20 O4P 21 21 214.8042; 7.6036; 37.247
90; 90; 90
1360.6Liu, Shuai; Dai, Haofu; Makhloufi, Gamall; Heering, Christian; Janiak, Christoph; Hartmann, Rudolf; Mándi, Attila; Kurtán, Tibor; Müller, Werner E G; Kassack, Matthias U.; Lin, Wenhan; Liu, Zhen; Proksch, Peter
Cytotoxic 14-Membered Macrolides from a Mangrove-Derived Endophytic Fungus, Pestalotiopsis microspora.
Journal of natural products, 2016, 79, 2332-2340
1553302 CIFC26 H40 O7P 1 21 110.0971; 6.95501; 18.0231
90; 100.84; 90
1243.1Kim, Jong Won; Ko, Sung-Kyun; Kim, Hye-Min; Kim, Gun-Hee; Son, Sangkeun; Kim, Gil Soo; Hwang, Gwi Ja; Jeon, Eun Soo; Shin, Kee-Sun; Ryoo, In-Ja; Hong, Young-Soo; Oh, Hyuncheol; Lee, Kyung Ho; Soung, Nak-Kyun; Hashizume, Daisuke; Nogawa, Toshihiko; Takahashi, Shunji; Kim, Bo Yeon; Osada, Hiroyuki; Jang, Jae-Hyuk; Ahn, Jong Seog
Stachybotrysin, an Osteoclast Differentiation Inhibitor from the Marine-Derived Fungus Stachybotrys sp. KCB13F013.
Journal of natural products, 2016, 79, 2703-2708
1553303 CIFC22 H30 O5P 21 21 216.5355; 12.797; 24.34
90; 90; 90
2035.7Xu, Jing; Wang, Meicheng; Sun, Xiaocong; Ren, Quanhui; Cao, Xiangrong; Li, Shen; Su, Guochen; Tuerhong, Muhetaer; Lee, Dongho; Ohizumi, Yasushi; Bartlam, Mark; Guo, Yuanqiang
Bioactive Terpenoids from Salvia plebeia: Structures, NO Inhibitory Activities, and Interactions with iNOS.
Journal of natural products, 2016, 79, 2924-2932
1553304 CIFC30 H42 O5P 21 21 216.37; 12.1724; 34.2046
90; 90; 90
2652.2Olivier, Wesley J.; Kilah, Nathan L.; Horne, James; Bissember, Alex C.; Smith, Jason A.
ent-Labdane Diterpenoids from Dodonaea viscosa.
Journal of natural products, 2016, 79, 3117-3126
1553305 CIFC30 H42 O5P 21 21 217.9309; 10.716; 31.529
90; 90; 90
2679.6Olivier, Wesley J.; Kilah, Nathan L.; Horne, James; Bissember, Alex C.; Smith, Jason A.
ent-Labdane Diterpenoids from Dodonaea viscosa.
Journal of natural products, 2016, 79, 3117-3126
1553306 CIFC28 H39 Cl O4C 1 2 129.0981; 8.0421; 11.3912
90; 104.315; 90
2582.9Olivier, Wesley J.; Kilah, Nathan L.; Horne, James; Bissember, Alex C.; Smith, Jason A.
ent-Labdane Diterpenoids from Dodonaea viscosa.
Journal of natural products, 2016, 79, 3117-3126
1553307 CIFC44.25 H74 N5 O11P 1 21 114.6436; 10.578; 15.5742
90; 92.794; 90
2409.58Almaliti, Jehad; Malloy, Karla L.; Glukhov, Evgenia; Spadafora, Carmenza; Gutiérrez, Marcelino; Gerwick, William H.
Dudawalamides A-D, Antiparasitic Cyclic Depsipeptides from the Marine Cyanobacterium Moorea producens.
Journal of natural products, 2017, 80, 1827-1836
1553308 CIFC19 H18 O2P 1 21/c 114.6675; 11.5099; 18.5162
90; 104.72; 90
3023.34Maurent, Kelly; Vanucci-Bacqué, Corinne; Saffon-Merceron, Nathalie; Baltas, Michel; Bedos-Belval, Florence
Total Synthesis of Tedarene A.
Journal of natural products, 2017, 80, 1623-1630
1553309 CIFC20 H20 O2P 1 21/n 19.3466; 12.3756; 14.0627
90; 98.832; 90
1607.34Maurent, Kelly; Vanucci-Bacqué, Corinne; Saffon-Merceron, Nathalie; Baltas, Michel; Bedos-Belval, Florence
Total Synthesis of Tedarene A.
Journal of natural products, 2017, 80, 1623-1630
1553310 CIFC20 H20 O2P 1 21 19.0364; 8.1877; 10.7482
90; 101.86; 90
778.25Maurent, Kelly; Vanucci-Bacqué, Corinne; Saffon-Merceron, Nathalie; Baltas, Michel; Bedos-Belval, Florence
Total Synthesis of Tedarene A.
Journal of natural products, 2017, 80, 1623-1630
1553311 CIFC19 H18 O2P -19.7921; 11.467; 13.899
88.098; 79.234; 79.122
1505.6Maurent, Kelly; Vanucci-Bacqué, Corinne; Saffon-Merceron, Nathalie; Baltas, Michel; Bedos-Belval, Florence
Total Synthesis of Tedarene A.
Journal of natural products, 2017, 80, 1623-1630
1553312 CIFC35 H44 O12P 21 21 215.7364; 19.8524; 11.454
90; 90; 90
3578.3Esposito, Mélissa; Nothias, Louis-Félix; Retailleau, Pascal; Costa, Jean; Roussi, Fanny; Neyts, Johan; Leyssen, Pieter; Touboul, David; Litaudon, Marc; Paolini, Julien
Isolation of Premyrsinane, Myrsinane, and Tigliane Diterpenoids from Euphorbia pithyusa Using a Chikungunya Virus Cell-Based Assay and Analogue Annotation by Molecular Networking.
Journal of natural products, 2017, 80, 2051-2059
1553313 CIFC14 H20 O4P 6515.7712; 15.7712; 10.4612
90; 90; 120
2253.42Li, Tian-Xiao; Liu, Rui-Huan; Wang, Xiao-Bing; Luo, Jun; Luo, Jian-Guang; Kong, Ling-Yi; Yang, Ming-Hua
Hypoxia-Protective Azaphilone Adducts from Peyronellaea glomerata.
Journal of natural products, 2018, 81, 1148-1153
1553314 CIFC15 H24 O2P 1 21 15.8459; 7.8647; 14.9863
90; 96.369; 90
684.76Zhou, Qin-Mei; Chen, Ming-Hua; Li, Xiao-Hong; Peng, Cheng; Lin, Da-Sheng; Li, Xiao-Nian; He, Yang; Xiong, Liang
Absolute Configurations and Bioactivities of Guaiane-Type Sesquiterpenoids Isolated from Pogostemon cablin.
Journal of natural products, 2018, 81, 1919-1927
1553315 CIFC15 H26 O2P 1 21 110.28; 15.493; 10.27
90; 119.71; 90
1420.7Zhou, Qin-Mei; Chen, Ming-Hua; Li, Xiao-Hong; Peng, Cheng; Lin, Da-Sheng; Li, Xiao-Nian; He, Yang; Xiong, Liang
Absolute Configurations and Bioactivities of Guaiane-Type Sesquiterpenoids Isolated from Pogostemon cablin.
Journal of natural products, 2018, 81, 1919-1927
1553316 CIFC15 H24 O2P 1 21 111.5078; 10.0306; 12.1928
90; 101.04; 90
1381.37Zhou, Qin-Mei; Chen, Ming-Hua; Li, Xiao-Hong; Peng, Cheng; Lin, Da-Sheng; Li, Xiao-Nian; He, Yang; Xiong, Liang
Absolute Configurations and Bioactivities of Guaiane-Type Sesquiterpenoids Isolated from Pogostemon cablin.
Journal of natural products, 2018, 81, 1919-1927
1553317 CIFC15 H24 O2P 1 21 17.5723; 9.7359; 9.3881
90; 102.926; 90
674.58Zhou, Qin-Mei; Chen, Ming-Hua; Li, Xiao-Hong; Peng, Cheng; Lin, Da-Sheng; Li, Xiao-Nian; He, Yang; Xiong, Liang
Absolute Configurations and Bioactivities of Guaiane-Type Sesquiterpenoids Isolated from Pogostemon cablin.
Journal of natural products, 2018, 81, 1919-1927
1553318 CIFC20 H26 O5P 1 21 111.6575; 9.7318; 15.2642
90; 93.137; 90
1729.11Hu, Hai-Jun; Zhou, Yue; Han, Zhu-Zhen; Shi, Yan-Hong; Zhang, Shu-Sheng; Wang, Zheng-Tao; Yang, Li
Abietane Diterpenoids from the Roots of Clerodendrum trichotomum and Their Nitric Oxide Inhibitory Activities.
Journal of natural products, 2018, 81, 1508-1516
1553319 CIFC20 H24 O5C 1 2 119.3772; 8.318; 11.812
90; 109.092; 90
1799.13Hu, Hai-Jun; Zhou, Yue; Han, Zhu-Zhen; Shi, Yan-Hong; Zhang, Shu-Sheng; Wang, Zheng-Tao; Yang, Li
Abietane Diterpenoids from the Roots of Clerodendrum trichotomum and Their Nitric Oxide Inhibitory Activities.
Journal of natural products, 2018, 81, 1508-1516
1553320 CIFC20 H22 O5P 21 21 218.2214; 10.0997; 20.3117
90; 90; 90
1686.56Hu, Hai-Jun; Zhou, Yue; Han, Zhu-Zhen; Shi, Yan-Hong; Zhang, Shu-Sheng; Wang, Zheng-Tao; Yang, Li
Abietane Diterpenoids from the Roots of Clerodendrum trichotomum and Their Nitric Oxide Inhibitory Activities.
Journal of natural products, 2018, 81, 1508-1516
1553321 CIFC19 H15 N O5P -16.93466; 9.91657; 11.54675
71.8945; 84.5865; 75.6285
730.985Zhang, Jun; Zhang, Qing-Ying; Tu, Peng-Fei; Xu, Fu-Chun; Liang, Hong
Mucroniferanines A-G, Isoquinoline Alkaloids from Corydalis mucronifera.
Journal of natural products, 2018, 81, 364-370
1553322 CIFC15 H24 O3P 21 21 211.3606; 13.5941; 9.1502
90; 90; 90
1413.13Xie, Shuangshuang; Wu, Ye; Qiao, Yuben; Guo, Yi; Wang, Jianping; Hu, Zhengxi; Zhang, Qing; Li, Xiaonian; Huang, Jinfeng; Zhou, Qun; Luo, Zengwei; Liu, Junjun; Zhu, Hucheng; Xue, Yongbo; Zhang, Yonghui
Protoilludane, Illudalane, and Botryane Sesquiterpenoids from the Endophytic Fungus Phomopsis sp. TJ507A.
Journal of natural products, 2018, 81, 1311-1320
1553323 CIFC16 H24 O3P -18.7757; 9.156; 9.8895
73.107; 85.312; 82.044
752.29Xie, Shuangshuang; Wu, Ye; Qiao, Yuben; Guo, Yi; Wang, Jianping; Hu, Zhengxi; Zhang, Qing; Li, Xiaonian; Huang, Jinfeng; Zhou, Qun; Luo, Zengwei; Liu, Junjun; Zhu, Hucheng; Xue, Yongbo; Zhang, Yonghui
Protoilludane, Illudalane, and Botryane Sesquiterpenoids from the Endophytic Fungus Phomopsis sp. TJ507A.
Journal of natural products, 2018, 81, 1311-1320
1553324 CIFC15 H20 O3P 21 21 217.9251; 11.9865; 14.2732
90; 90; 90
1355.87Xie, Shuangshuang; Wu, Ye; Qiao, Yuben; Guo, Yi; Wang, Jianping; Hu, Zhengxi; Zhang, Qing; Li, Xiaonian; Huang, Jinfeng; Zhou, Qun; Luo, Zengwei; Liu, Junjun; Zhu, Hucheng; Xue, Yongbo; Zhang, Yonghui
Protoilludane, Illudalane, and Botryane Sesquiterpenoids from the Endophytic Fungus Phomopsis sp. TJ507A.
Journal of natural products, 2018, 81, 1311-1320
1553325 CIFC26.5 H31 F N O6P 1 21 19.4144; 25.4932; 10.9393
90; 115.504; 90
2369.63Egbewande, Folake A.; Sadowski, Martin C.; Levrier, Claire; Tousignant, Kaylyn D.; White, Jonathan M.; Coster, Mark J.; Nelson, Colleen C.; Davis, Rohan A.
Identification of Gibberellic Acid Derivatives That Deregulate Cholesterol Metabolism in Prostate Cancer Cells.
Journal of natural products, 2018, 81, 838-845
1553326 CIFC9 H9 N O3P b c a8.7826; 13.1341; 16.1714
90; 90; 90
1865.4Chang, Fang-Rong; Li, Pei-Shian; Huang Liu, Rosa; Hu, Hao-Chun; Hwang, Tsong-Long; Lee, Jin-Ching; Chen, Shu-Li; Wu, Yang-Chang; Cheng, Yuan-Bin
Bioactive Phenolic Components from the Twigs of Atalantia buxifolia.
Journal of natural products, 2018, 81, 1534-1539
1553327 CIFC20 H34 O5P 1 21 16.6038; 20.8285; 7.1958
90; 112.565; 90
913.99Zhu, Yu-Xun; Zhang, Zhao-Xin; Yan, Hui-Min; Lu, Di; Zhang, Huan-Ping; Li, Li; Liu, Yun-Bao; Li, Yong
Antinociceptive Diterpenoids from the Leaves and Twigs of Rhododendron decorum.
Journal of natural products, 2018, 81, 1183-1192
1553328 CIFC16 H13 N O4P 1 21/c 17.4572; 8.9283; 18.5642
90; 92.91; 90
1234.4Ndongo, Joseph T.; Mbing, Joséphine N; Monteillier, Aymeric; Tala, Michel F.; Rütten, Michael; Mombers, Daniel; Cuendet, Muriel; Pegnyemb, Dieudonné E; Dittrich, Birger; Laatsch, Hartmut
Carbazole-, Aspidofractinine-, and Aspidocarpamine-Type Alkaloids from Pleiocarpa pycnantha.
Journal of natural products, 2018, 81, 1193-1202
1553329 CIFC23 H28 N2 O4P 1 21 17.4061; 9.1421; 14.8478
90; 95.826; 90
1000.11Ndongo, Joseph T.; Mbing, Joséphine N; Monteillier, Aymeric; Tala, Michel F.; Rütten, Michael; Mombers, Daniel; Cuendet, Muriel; Pegnyemb, Dieudonné E; Dittrich, Birger; Laatsch, Hartmut
Carbazole-, Aspidofractinine-, and Aspidocarpamine-Type Alkaloids from Pleiocarpa pycnantha.
Journal of natural products, 2018, 81, 1193-1202
1553330 CIFC20 H28 O4P 21 21 218.8766; 10.9773; 18.104
90; 90; 90
1764.07Qi, Xiao-Li; Zhang, Ying-Ying; Zhao, Peng; Zhou, Le; Wang, Xiao-Bo; Huang, Xiao-Xiao; Lin, Bin; Song, Shao-Jiang
ent-Kaurane Diterpenoids with Neuroprotective Properties from Corn Silk ( Zea mays).
Journal of natural products, 2018, 81, 1225-1234
1553331 CIFC12 H12 O6P 21 21 214.7901; 19.0871; 8.0499
90; 90; 90
2272.49Cai, Runlin; Wu, Yingnan; Chen, Senhua; Cui, Hui; Liu, Zhaoming; Li, Chunyuan; She, Zhigang
Peniisocoumarins A-J: Isocoumarins from Penicillium commune QQF-3, an Endophytic Fungus of the Mangrove Plant Kandelia candel.
Journal of natural products, 2018, 81, 1376-1383
1553332 CIFC28 H24 O12I 1 2/a 127.9933; 9.57267; 22.8556
90; 118.274; 90
5393.91Cai, Runlin; Wu, Yingnan; Chen, Senhua; Cui, Hui; Liu, Zhaoming; Li, Chunyuan; She, Zhigang
Peniisocoumarins A-J: Isocoumarins from Penicillium commune QQF-3, an Endophytic Fungus of the Mangrove Plant Kandelia candel.
Journal of natural products, 2018, 81, 1376-1383
1553333 CIFC28 H24 O12P -18.1894; 10.3069; 15.1113
82.627; 87.492; 76.457
1229.66Cai, Runlin; Wu, Yingnan; Chen, Senhua; Cui, Hui; Liu, Zhaoming; Li, Chunyuan; She, Zhigang
Peniisocoumarins A-J: Isocoumarins from Penicillium commune QQF-3, an Endophytic Fungus of the Mangrove Plant Kandelia candel.
Journal of natural products, 2018, 81, 1376-1383
1553334 CIFC13 H13 Cl O5C 1 2 122.066; 9.1694; 6.5996
90; 107.302; 90
1274.89Cai, Runlin; Wu, Yingnan; Chen, Senhua; Cui, Hui; Liu, Zhaoming; Li, Chunyuan; She, Zhigang
Peniisocoumarins A-J: Isocoumarins from Penicillium commune QQF-3, an Endophytic Fungus of the Mangrove Plant Kandelia candel.
Journal of natural products, 2018, 81, 1376-1383
1553335 CIFC13 H15 Cl O7P 15.0238; 5.5679; 12.8812
99.395; 94.679; 105.645
339.31Cai, Runlin; Wu, Yingnan; Chen, Senhua; Cui, Hui; Liu, Zhaoming; Li, Chunyuan; She, Zhigang
Peniisocoumarins A-J: Isocoumarins from Penicillium commune QQF-3, an Endophytic Fungus of the Mangrove Plant Kandelia candel.
Journal of natural products, 2018, 81, 1376-1383
1553336 CIFC15 H14 O6P 21 21 214.5542; 11.4674; 25.3578
90; 90; 90
1324.31Cai, Runlin; Wu, Yingnan; Chen, Senhua; Cui, Hui; Liu, Zhaoming; Li, Chunyuan; She, Zhigang
Peniisocoumarins A-J: Isocoumarins from Penicillium commune QQF-3, an Endophytic Fungus of the Mangrove Plant Kandelia candel.
Journal of natural products, 2018, 81, 1376-1383
1553337 CIFC20 H26 O3P 21 21 216.6328; 11.7781; 22.7943
90; 90; 90
1780.73Zhang, Chun-Yan; Zhang, Li-Jun; Lu, Zhi-Cheng; Ma, Chen-Yun; Ye, Ying; Rahman, Khalid; Zhang, Hong; Zhu, Jian-Yong
Antitumor Activity of Diterpenoids from Jatropha gossypiifolia: Cell Cycle Arrest and Apoptosis-Inducing Activity in RKO Colon Cancer Cells.
Journal of natural products, 2018, 81, 1701-1710
1553338 CIFC22 H30 O4P 21 21 218.9197; 13.6933; 16.4126
90; 90; 90
2004.64Zhang, Chun-Yan; Zhang, Li-Jun; Lu, Zhi-Cheng; Ma, Chen-Yun; Ye, Ying; Rahman, Khalid; Zhang, Hong; Zhu, Jian-Yong
Antitumor Activity of Diterpenoids from Jatropha gossypiifolia: Cell Cycle Arrest and Apoptosis-Inducing Activity in RKO Colon Cancer Cells.
Journal of natural products, 2018, 81, 1701-1710
1553339 CIFC22 H30 O4P 21 21 210.775; 20.705; 9.606
90; 90; 90
2143.1Zhang, Chun-Yan; Zhang, Li-Jun; Lu, Zhi-Cheng; Ma, Chen-Yun; Ye, Ying; Rahman, Khalid; Zhang, Hong; Zhu, Jian-Yong
Antitumor Activity of Diterpenoids from Jatropha gossypiifolia: Cell Cycle Arrest and Apoptosis-Inducing Activity in RKO Colon Cancer Cells.
Journal of natural products, 2018, 81, 1701-1710
1553340 CIFC12 H18 O8P 21 21 216.7584; 14.2353; 27.7506
90; 90; 90
2669.83Deans, Bianca J.; Kilah, Nathan L.; Jordan, Gregory J.; Bissember, Alex C.; Smith, Jason A.
Arbutin Derivatives Isolated from Ancient Proteaceae: Potential Phytochemical Markers Present in Bellendena, Cenarrhenes, and Persoonia Genera.
Journal of natural products, 2018, 81, 1241-1251
1553341 CIFC22 H28 O11P 1 21 114.958; 4.754; 15.974
90; 100.84; 90
1115.6Deans, Bianca J.; Kilah, Nathan L.; Jordan, Gregory J.; Bissember, Alex C.; Smith, Jason A.
Arbutin Derivatives Isolated from Ancient Proteaceae: Potential Phytochemical Markers Present in Bellendena, Cenarrhenes, and Persoonia Genera.
Journal of natural products, 2018, 81, 1241-1251
1553342 CIFC17 H22 O9P 14.9; 12.5; 14.55
86.4; 88.07; 80.31
876.5Deans, Bianca J.; Kilah, Nathan L.; Jordan, Gregory J.; Bissember, Alex C.; Smith, Jason A.
Arbutin Derivatives Isolated from Ancient Proteaceae: Potential Phytochemical Markers Present in Bellendena, Cenarrhenes, and Persoonia Genera.
Journal of natural products, 2018, 81, 1241-1251
1553343 CIFC17 H24 O10C 1 2 114.2391; 6.4146; 19.8531
90; 95.8796; 90
1803.81Deans, Bianca J.; Kilah, Nathan L.; Jordan, Gregory J.; Bissember, Alex C.; Smith, Jason A.
Arbutin Derivatives Isolated from Ancient Proteaceae: Potential Phytochemical Markers Present in Bellendena, Cenarrhenes, and Persoonia Genera.
Journal of natural products, 2018, 81, 1241-1251
1553344 CIFC21 H22 O10P 21 21 215.353; 17.855; 19.903
90; 90; 90
1902.3Deans, Bianca J.; Kilah, Nathan L.; Jordan, Gregory J.; Bissember, Alex C.; Smith, Jason A.
Arbutin Derivatives Isolated from Ancient Proteaceae: Potential Phytochemical Markers Present in Bellendena, Cenarrhenes, and Persoonia Genera.
Journal of natural products, 2018, 81, 1241-1251
1553345 CIFC27 H36 O8I 427.2552; 27.2552; 7.0051
90; 90; 90
5203.71Qi, Changxing; Liu, Mengting; Zhou, Qun; Gao, Weixi; Chen, Chunmei; Lai, Yongji; Hu, Zhengxi; Xue, Yongbo; Zhang, Jinwen; Li, Dongyan; Li, Xiao-Nian; Zhang, Qing; Wang, Jianping; Zhu, Hucheng; Zhang, Yonghui
BACE1 Inhibitory Meroterpenoids from Aspergillus terreus.
Journal of natural products, 2018, 81, 1937-1945
1553346 CIFC26 H34 O8P 21 21 218.0835; 14.1264; 21.173
90; 90; 90
2417.76Qi, Changxing; Liu, Mengting; Zhou, Qun; Gao, Weixi; Chen, Chunmei; Lai, Yongji; Hu, Zhengxi; Xue, Yongbo; Zhang, Jinwen; Li, Dongyan; Li, Xiao-Nian; Zhang, Qing; Wang, Jianping; Zhu, Hucheng; Zhang, Yonghui
BACE1 Inhibitory Meroterpenoids from Aspergillus terreus.
Journal of natural products, 2018, 81, 1937-1945
1553347 CIFC27 H40 O9P 21 21 217.8574; 11.5792; 28.3079
90; 90; 90
2575.52Qi, Changxing; Liu, Mengting; Zhou, Qun; Gao, Weixi; Chen, Chunmei; Lai, Yongji; Hu, Zhengxi; Xue, Yongbo; Zhang, Jinwen; Li, Dongyan; Li, Xiao-Nian; Zhang, Qing; Wang, Jianping; Zhu, Hucheng; Zhang, Yonghui
BACE1 Inhibitory Meroterpenoids from Aspergillus terreus.
Journal of natural products, 2018, 81, 1937-1945
1553348 CIFC26 H34 O8P 16.5706; 7.0972; 13.8873
103.479; 90.068; 105.91
604.17Qi, Changxing; Liu, Mengting; Zhou, Qun; Gao, Weixi; Chen, Chunmei; Lai, Yongji; Hu, Zhengxi; Xue, Yongbo; Zhang, Jinwen; Li, Dongyan; Li, Xiao-Nian; Zhang, Qing; Wang, Jianping; Zhu, Hucheng; Zhang, Yonghui
BACE1 Inhibitory Meroterpenoids from Aspergillus terreus.
Journal of natural products, 2018, 81, 1937-1945
1553349 CIFC26 H30 O9P 1 21 118.2722; 8.8097; 30.3644
90; 106.554; 90
4685.2Qi, Changxing; Liu, Mengting; Zhou, Qun; Gao, Weixi; Chen, Chunmei; Lai, Yongji; Hu, Zhengxi; Xue, Yongbo; Zhang, Jinwen; Li, Dongyan; Li, Xiao-Nian; Zhang, Qing; Wang, Jianping; Zhu, Hucheng; Zhang, Yonghui
BACE1 Inhibitory Meroterpenoids from Aspergillus terreus.
Journal of natural products, 2018, 81, 1937-1945
1553350 CIFC26 H34 O7P 1 21 112.239; 8.3534; 23.758
90; 97.666; 90
2407.2Qi, Changxing; Liu, Mengting; Zhou, Qun; Gao, Weixi; Chen, Chunmei; Lai, Yongji; Hu, Zhengxi; Xue, Yongbo; Zhang, Jinwen; Li, Dongyan; Li, Xiao-Nian; Zhang, Qing; Wang, Jianping; Zhu, Hucheng; Zhang, Yonghui
BACE1 Inhibitory Meroterpenoids from Aspergillus terreus.
Journal of natural products, 2018, 81, 1937-1945
1553351 CIFC15 H24 O2P 21 21 216.02825; 12.9002; 17.5524
90; 90; 90
1364.97Zhang, Ruifei; Feng, Xiao; Su, Guozhu; Mu, Zejing; Zhang, Hexinge; Zhao, Yanan; Jiao, Shungang; Cao, Lan; Chen, Suyile; Tu, Pengfei; Chai, Xingyun
Bioactive Sesquiterpenoids from the Peeled Stems of Syringa pinnatifolia.
Journal of natural products, 2018, 81, 1711-1720
1553352 CIFC16 H26 O3P -17.4903; 10.5587; 11.233
63.805; 72.976; 85.623
760.77Zhang, Ruifei; Feng, Xiao; Su, Guozhu; Mu, Zejing; Zhang, Hexinge; Zhao, Yanan; Jiao, Shungang; Cao, Lan; Chen, Suyile; Tu, Pengfei; Chai, Xingyun
Bioactive Sesquiterpenoids from the Peeled Stems of Syringa pinnatifolia.
Journal of natural products, 2018, 81, 1711-1720
1553353 CIFC15 H26 OP 1 21 16.0061; 25.4056; 13.9957
90; 92.894; 90
2132.86Zhang, Ruifei; Feng, Xiao; Su, Guozhu; Mu, Zejing; Zhang, Hexinge; Zhao, Yanan; Jiao, Shungang; Cao, Lan; Chen, Suyile; Tu, Pengfei; Chai, Xingyun
Bioactive Sesquiterpenoids from the Peeled Stems of Syringa pinnatifolia.
Journal of natural products, 2018, 81, 1711-1720
1553354 CIFC15 H24 O2P 21 21 216.0342; 12.8921; 17.5406
90; 90; 90
1364.54Zhang, Ruifei; Feng, Xiao; Su, Guozhu; Mu, Zejing; Zhang, Hexinge; Zhao, Yanan; Jiao, Shungang; Cao, Lan; Chen, Suyile; Tu, Pengfei; Chai, Xingyun
Bioactive Sesquiterpenoids from the Peeled Stems of Syringa pinnatifolia.
Journal of natural products, 2018, 81, 1711-1720
1553355 CIFC29.25 H43 O3.25C 1 2 145.884; 7.0425; 15.7032
90; 103.902; 90
4925.7Liu, Fei; Wang, Ya-Nan; Li, Yong; Ma, Shuang-Gang; Qu, Jing; Liu, Yun-Bao; Niu, Chang-Shan; Tang, Zhong-Hai; Li, Yu-Huan; Li, Li; Yu, Shi-Shan
Minor Nortriterpenoids from the Twigs and Leaves of Rhododendron latoucheae.
Journal of natural products, 2018, 81, 1721-1733
1553356 CIFC34 H48 O10P -19.8858; 12.0145; 14.3049
89.442; 76.043; 85.25
1643.12Li, Yan-Ping; Hu, Kun; Yang, Xing-Wei; Xu, Gang
Antibacterial Dimeric Acylphloroglucinols from Hypericum japonicum.
Journal of natural products, 2018, 81, 1098-1102
1553357 CIFC10 H8 N O3P -16.7548; 7.6045; 8.7945
109.953; 90.989; 98.977
418.22Ghate, Nikhil B.; Chaudhuri, Dipankar; Panja, Sourav; Singh, Sudhir S.; Gupta, Gajendra; Lee, Chang Yeon; Mandal, Nripendranath
In Vitro Mechanistic Study of the Anti-inflammatory Activity of a Quinoline Isolated from Spondias pinnata Bark.
Journal of natural products, 2018, 81, 1956-1961
1553358 CIFC15 H19 Cl N2 O6P 21 21 217.1002; 12.6795; 18.118
90; 90; 90
1631.1Fitch, Richard W.; Snider, Barry B.; Zhou, Quan; Foxman, Bruce M.; Pandya, Anshul A.; Yakel, Jerrel L.; Olson, Thao T.; Al-Muhtasib, Nour; Xiao, Yingxian; Welch, Kevin D.; Panter, Kip E.
Absolute Configuration and Pharmacology of the Poison Frog Alkaloid Phantasmidine.
Journal of natural products, 2018, 81, 1029-1035
1553359 CIFC20 H20 O7P 1 21 18.3572; 11.9056; 9.5276
90; 110.117; 90
890.14Ren, Fengxia; Chen, Shenxi; Zhang, Yang; Zhu, Shuaiming; Xiao, Junhai; Liu, Xingzhong; Su, Ruibin; Che, Yongsheng
Hawaiienols A-D, Highly Oxygenated p-Terphenyls from an Insect-Associated Fungus, Paraconiothyrium hawaiiense.
Journal of natural products, 2018, 81, 1752-1759
1553360 CIFC24 H39 N O7P 18.054; 12.548; 14.0945
115.86; 94.702; 102.435
1226.37Wang, Wenjing; Gong, Jiaojiao; Liu, Xiaorui; Dai, Chong; Wang, Yanyan; Li, Xiao-Nian; Wang, Jianping; Luo, Zengwei; Zhou, Yuan; Xue, Yongbo; Zhu, Hucheng; Chen, Chunmei; Zhang, Yonghui
Cytochalasans Produced by the Coculture of Aspergillus flavipes and Chaetomium globosum.
Journal of natural products, 2018, 81, 1578-1587
1553361 CIFC17 H18 O4P 21 21 217.4196; 10.8293; 17.811
90; 90; 90
1431.1Shi, Zhen-Zhen; Miao, Feng-Ping; Fang, Sheng-Tao; Yin, Xiu-Li; Ji, Nai-Yun
Trichorenins A-C, Algicidal Tetracyclic Metabolites from the Marine-Alga-Epiphytic Fungus Trichoderma virens Y13-3.
Journal of natural products, 2018, 81, 1121-1124
1553362 CIFC20 H28 N2 O5P 1 21 18.2777; 11.3247; 10.202
90; 94.708; 90
953.13Yeap, Joanne Soon-Yee; Navanesan, Suerialoasan; Sim, Kae-Shin; Yong, Kien-Thai; Gurusamy, Subramaniam; Lim, Siew-Huah; Low, Yun-Yee; Kam, Toh-Seok
Ajmaline, Oxindole, and Cytotoxic Macroline-Akuammiline Bisindole Alkaloids from Alstonia penangiana.
Journal of natural products, 2018, 81, 1266-1277
1553363 CIFC45 H56 Cl6 N4 O5P 1 21 19.4917; 12.8453; 18.5275
90; 99.113; 90
2230.4Yeap, Joanne Soon-Yee; Navanesan, Suerialoasan; Sim, Kae-Shin; Yong, Kien-Thai; Gurusamy, Subramaniam; Lim, Siew-Huah; Low, Yun-Yee; Kam, Toh-Seok
Ajmaline, Oxindole, and Cytotoxic Macroline-Akuammiline Bisindole Alkaloids from Alstonia penangiana.
Journal of natural products, 2018, 81, 1266-1277
1553364 CIFC37 H54 O12P 21 21 2112.5134; 15.207; 20.2912
90; 90; 90
3861.24Ye, Ye; Dawa, Drolma; Liu, Guang-Hui; Zhao, Min; Tseden, Dorje; Gu, Yu-Cheng; Ding, Li-Sheng; Cao, Zhi-Xing; Zhou, Yan
Antiproliferative Sesquiterpenoids from Ligularia rumicifolia with Diverse Skeletons.
Journal of natural products, 2018, 81, 1992-2003
1553365 CIFC30 H45 O5P 1 21 17.2485; 11.0572; 17.0554
90; 99.689; 90
1347.46Bai, Wei; Yang, Hong-Ying; Jiao, Xing-Zhi; Feng, Ke-Na; Chen, Jian-Jun; Gao, Kun
Structurally Diverse Highly Oxygenated Triterpenoids from the Roots of Ailanthus altissima and Their Cytotoxicity.
Journal of natural products, 2018, 81, 1777-1785
1553366 CIFC17 H14 O7P 1 21/n 19.176; 8.194; 19.269
90; 93.524; 90
1446.1Olivon, Florent; Nothias, Louis-Félix; Dumontet, Vincent; Retailleau, Pascal; Berger, Sylvie; Ferry, Gilles; Cohen, William; Pfeiffer, Bruno; Boutin, Jean A.; Scalbert, Elisabeth; Roussi, Fanny; Litaudon, Marc
Natural Inhibitors of the RhoA-p115 Complex from the Bark of Meiogyne baillonii.
Journal of natural products, 2018, 81, 1610-1618
1553367 CIFC19 H28 O7P 21 21 219.2199; 11.2065; 19.177
90; 90; 90
1981.42Yu, Zhang-Xin; Zheng, Cai-Juan; Chen, Guang-Ying; Huang, Rong-Li; Zhou, Xue-Ming; Niu, Zhi-Gang; Li, Xiao-Bao; Han, Chang-Ri; Song, Xiao-Ping
3,4- seco-Norclerodane Diterpenoids from the Roots of Polyalthia laui.
Journal of natural products, 2019, 82, 27-34
1553368 CIFC21 H30 O4P 21 21 217.02787; 11.2128; 24.3184
90; 90; 90
1916.34Yu, Zhang-Xin; Zheng, Cai-Juan; Chen, Guang-Ying; Huang, Rong-Li; Zhou, Xue-Ming; Niu, Zhi-Gang; Li, Xiao-Bao; Han, Chang-Ri; Song, Xiao-Ping
3,4- seco-Norclerodane Diterpenoids from the Roots of Polyalthia laui.
Journal of natural products, 2019, 82, 27-34
1553369 CIFC20 H34 O5P 21 21 217.22366; 15.7069; 17.8026
90; 90; 90
2019.91Yu, Zhang-Xin; Zheng, Cai-Juan; Chen, Guang-Ying; Huang, Rong-Li; Zhou, Xue-Ming; Niu, Zhi-Gang; Li, Xiao-Bao; Han, Chang-Ri; Song, Xiao-Ping
3,4- seco-Norclerodane Diterpenoids from the Roots of Polyalthia laui.
Journal of natural products, 2019, 82, 27-34
1553370 CIFC19 H30 O5P 1 21 18.2372; 25.7913; 9.2037
90; 102.626; 90
1908.02Yu, Zhang-Xin; Zheng, Cai-Juan; Chen, Guang-Ying; Huang, Rong-Li; Zhou, Xue-Ming; Niu, Zhi-Gang; Li, Xiao-Bao; Han, Chang-Ri; Song, Xiao-Ping
3,4- seco-Norclerodane Diterpenoids from the Roots of Polyalthia laui.
Journal of natural products, 2019, 82, 27-34
1553371 CIFC17.5 H24 O3.5P 21 21 2110.272; 16.583; 18.9486
90; 90; 90
3227.72Huang, Guang-Hui; Hu, Zhu; Lei, Chun; Wang, Pei-Pei; Yang, Jing; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Enantiomeric Pairs of Meroterpenoids with Diverse Heterocyclic Systems from Rhododendron nyingchiense.
Journal of natural products, 2018, 81, 1810-1818
1553372 CIFC17 H22 O2C 1 2 129.658; 6.8498; 7.4333
90; 104.45; 90
1462.31Huang, Guang-Hui; Hu, Zhu; Lei, Chun; Wang, Pei-Pei; Yang, Jing; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Enantiomeric Pairs of Meroterpenoids with Diverse Heterocyclic Systems from Rhododendron nyingchiense.
Journal of natural products, 2018, 81, 1810-1818
1553373 CIFC17 H22 O2P 21 21 216.0879; 8.0119; 29.617
90; 90; 90
1444.59Huang, Guang-Hui; Hu, Zhu; Lei, Chun; Wang, Pei-Pei; Yang, Jing; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Enantiomeric Pairs of Meroterpenoids with Diverse Heterocyclic Systems from Rhododendron nyingchiense.
Journal of natural products, 2018, 81, 1810-1818
1553374 CIFC17 H24 O5P 21 21 219.3465; 9.3699; 18.6281
90; 90; 90
1631.37Huang, Guang-Hui; Hu, Zhu; Lei, Chun; Wang, Pei-Pei; Yang, Jing; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Enantiomeric Pairs of Meroterpenoids with Diverse Heterocyclic Systems from Rhododendron nyingchiense.
Journal of natural products, 2018, 81, 1810-1818
1553375 CIFC18 H26 O3P 21 21 2110.1815; 10.1849; 15.7912
90; 90; 90
1637.51Huang, Guang-Hui; Hu, Zhu; Lei, Chun; Wang, Pei-Pei; Yang, Jing; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Enantiomeric Pairs of Meroterpenoids with Diverse Heterocyclic Systems from Rhododendron nyingchiense.
Journal of natural products, 2018, 81, 1810-1818
1553376 CIFC21 H32 O3P 16.2785; 10.5538; 14.393
100.197; 100.924; 91.722
919.64Zhang, Shasha; Wang, Xia; Hao, Jin; Li, Dangdang; Csuk, René; Li, Shengkun
Expediently Scalable Synthesis and Antifungal Exploration of (+)-Yahazunol and Related Meroterpenoids.
Journal of natural products, 2018, 81, 2010-2017
1553377 CIFC20 H16 N2 O3C 1 c 125.67; 7.0317; 17.015
90; 103.786; 90
2982.8Liu, Ye; Yu, Heng-Yi; Xu, Hong-Zhe; Liu, Jun-Jun; Meng, Xiang-Gao; Zhou, Ming; Ruan, Han-Li
Alkaloids with Immunosuppressive Activity from the Bark of Pausinystalia yohimbe.
Journal of natural products, 2018, 81, 1841-1849
1553378 CIFC20 H18 N2 O4P 1 21/n 110.596; 19.264; 16.921
90; 106.312; 90
3314.9Liu, Ye; Yu, Heng-Yi; Xu, Hong-Zhe; Liu, Jun-Jun; Meng, Xiang-Gao; Zhou, Ming; Ruan, Han-Li
Alkaloids with Immunosuppressive Activity from the Bark of Pausinystalia yohimbe.
Journal of natural products, 2018, 81, 1841-1849
1553379 CIFC29 H35 N O3P b c a12.9258; 18.5966; 20.6239
90; 90; 90
4957.49Ma, Xiao-Li; Li, Jun; Zheng, Jiao; Gu, Xiao-Pan; Ferreira, Daneel; Zjawiony, Jordan K.; Zhao, Ming-Bo; Guo, Xiao-Yu; Tu, Peng-Fei; Jiang, Yong
LC-MS-Guided Isolation of Insulin-Secretion-Promoting Monoterpenoid Carbazole Alkaloids from Murraya microphylla.
Journal of natural products, 2018, 81, 2371-2380
1553380 CIFC29 H35 N O3P 1 21 17.72842; 10.28179; 15.3023
90; 91.9454; 90
1215.25Ma, Xiao-Li; Li, Jun; Zheng, Jiao; Gu, Xiao-Pan; Ferreira, Daneel; Zjawiony, Jordan K.; Zhao, Ming-Bo; Guo, Xiao-Yu; Tu, Peng-Fei; Jiang, Yong
LC-MS-Guided Isolation of Insulin-Secretion-Promoting Monoterpenoid Carbazole Alkaloids from Murraya microphylla.
Journal of natural products, 2018, 81, 2371-2380
1553381 CIFC15 H18 O6P 1 21 15.6966; 5.6223; 22.2355
90; 95.895; 90
708.39Pang, Xiaoyan; Lin, Xiuping; Yang, Jie; Zhou, Xuefeng; Yang, Bin; Wang, Junfeng; Liu, Yonghong
Spiro-Phthalides and Isocoumarins Isolated from the Marine-Sponge-Derived Fungus Setosphaeria sp. SCSIO41009.
Journal of natural products, 2018, 81, 1860-1868
1553382 CIFC16 H20 O7P 21 21 217.73476; 8.02415; 25.5244
90; 90; 90
1584.17Pang, Xiaoyan; Lin, Xiuping; Yang, Jie; Zhou, Xuefeng; Yang, Bin; Wang, Junfeng; Liu, Yonghong
Spiro-Phthalides and Isocoumarins Isolated from the Marine-Sponge-Derived Fungus Setosphaeria sp. SCSIO41009.
Journal of natural products, 2018, 81, 1860-1868
1553383 CIFC11 H14 O5P 1 21/n 14.2311; 13.8888; 18.56
90; 91.894; 90
1090.1Pang, Xiaoyan; Lin, Xiuping; Yang, Jie; Zhou, Xuefeng; Yang, Bin; Wang, Junfeng; Liu, Yonghong
Spiro-Phthalides and Isocoumarins Isolated from the Marine-Sponge-Derived Fungus Setosphaeria sp. SCSIO41009.
Journal of natural products, 2018, 81, 1860-1868
1553384 CIFC20 H32 O5P 1 21 111.0078; 6.8749; 12.6547
90; 98.677; 90
946.72Wei, Wen-Jun; Song, Qiu-Yan; Zheng, Zai-Qin; Yao, Xiaojun; Li, Ya; Gao, Kun
Phytotoxic ent-Isopimarane-Type Diterpenoids from Euphorbia hylonoma.
Journal of natural products, 2018, 81, 2381-2391
1553385 CIFC18 H26 O6P 21 21 216.7154; 15.1719; 17.1256
90; 90; 90
1744.8Xiong, Juan; Wang, Li-Jun; Qian, Jianchang; Wang, Pei-Pei; Wang, Xue-Jiao; Ma, Guang-Lei; Zeng, Huaqiang; Li, Jia; Hu, Jin-Feng
Structurally Diverse Sesquiterpenoids from the Endangered Ornamental Plant Michelia shiluensis.
Journal of natural products, 2018, 81, 2195-2204
1553386 CIFC18 H26 O7P 1 21 110.7912; 7.2246; 11.6007
90; 96.97; 90
897.73Xiong, Juan; Wang, Li-Jun; Qian, Jianchang; Wang, Pei-Pei; Wang, Xue-Jiao; Ma, Guang-Lei; Zeng, Huaqiang; Li, Jia; Hu, Jin-Feng
Structurally Diverse Sesquiterpenoids from the Endangered Ornamental Plant Michelia shiluensis.
Journal of natural products, 2018, 81, 2195-2204
1553387 CIFC19 H26 O7P 1 21 18.9106; 10.0011; 11.0207
90; 110.689; 90
918.78Xiong, Juan; Wang, Li-Jun; Qian, Jianchang; Wang, Pei-Pei; Wang, Xue-Jiao; Ma, Guang-Lei; Zeng, Huaqiang; Li, Jia; Hu, Jin-Feng
Structurally Diverse Sesquiterpenoids from the Endangered Ornamental Plant Michelia shiluensis.
Journal of natural products, 2018, 81, 2195-2204
1553388 CIFC19 H23 O6.5P 21 21 218.32583; 13.41861; 29.848
90; 90; 90
3334.65Huang, Hongbo; Song, Yongxiang; Li, Xin; Wang, Xin; Ling, Chunyao; Qin, Xiangjing; Zhou, Zhenbin; Li, Qinglian; Wei, Xiaoyi; Ju, Jianhua
Abyssomicin Monomers and Dimers from the Marine-Derived Streptomyces koyangensis SCSIO 5802.
Journal of natural products, 2018, 81, 1892-1898
1553389 CIFC19 H24 O7P 21 21 216.6414; 14.9068; 17.8924
90; 90; 90
1771.38Huang, Hongbo; Song, Yongxiang; Li, Xin; Wang, Xin; Ling, Chunyao; Qin, Xiangjing; Zhou, Zhenbin; Li, Qinglian; Wei, Xiaoyi; Ju, Jianhua
Abyssomicin Monomers and Dimers from the Marine-Derived Streptomyces koyangensis SCSIO 5802.
Journal of natural products, 2018, 81, 1892-1898
1553390 CIFC38 H50 O14 SP 6213.403; 13.403; 17.8604
90; 90; 120
2778.6Huang, Hongbo; Song, Yongxiang; Li, Xin; Wang, Xin; Ling, Chunyao; Qin, Xiangjing; Zhou, Zhenbin; Li, Qinglian; Wei, Xiaoyi; Ju, Jianhua
Abyssomicin Monomers and Dimers from the Marine-Derived Streptomyces koyangensis SCSIO 5802.
Journal of natural products, 2018, 81, 1892-1898
1553391 CIFC20 H32 O2C 1 2 136.457; 4.886; 20.2686
90; 105.385; 90
3481Raghavan, Vijay; Johnson, Jordan L.; Stec, Donald F.; Song, Bongkeun; Zajac, Grzegorz; Baranska, Malgorzata; Harris, Constance M.; Schley, Nathan D.; Polavarapu, Prasad L.; Harris, Thomas M.
Absolute Configurations of Naturally Occurring [5]- and [3]-Ladderanoic Acids: Isolation, Chiroptical Spectroscopy, and Crystallography.
Journal of natural products, 2018, 81, 2654-2666
1553392 CIFC20 H30 O2C 1 2 164.164; 4.8171; 10.9786
90; 90.556; 90
3393.2Raghavan, Vijay; Johnson, Jordan L.; Stec, Donald F.; Song, Bongkeun; Zajac, Grzegorz; Baranska, Malgorzata; Harris, Constance M.; Schley, Nathan D.; Polavarapu, Prasad L.; Harris, Thomas M.
Absolute Configurations of Naturally Occurring [5]- and [3]-Ladderanoic Acids: Isolation, Chiroptical Spectroscopy, and Crystallography.
Journal of natural products, 2018, 81, 2654-2666
1553393 CIFC28 H36 O3P 1 21 15.3774; 14.7492; 43.061
90; 90.817; 90
3414.9Raghavan, Vijay; Johnson, Jordan L.; Stec, Donald F.; Song, Bongkeun; Zajac, Grzegorz; Baranska, Malgorzata; Harris, Constance M.; Schley, Nathan D.; Polavarapu, Prasad L.; Harris, Thomas M.
Absolute Configurations of Naturally Occurring [5]- and [3]-Ladderanoic Acids: Isolation, Chiroptical Spectroscopy, and Crystallography.
Journal of natural products, 2018, 81, 2654-2666
1553394 CIFC26.5 H50 O11.5P 1 21 16.3352; 39.6779; 11.4316
90; 90.621; 90
2873.4Sun, Na; Zhu, Yan; Zhou, Haofeng; Zhou, Junfei; Zhang, Hanqi; Zhang, Mengke; Zeng, Hong; Yao, Guangmin
Grayanane Diterpenoid Glucosides from the Leaves of Rhododendron micranthum and Their Bioactivities Evaluation.
Journal of natural products, 2018, 81, 2673-2681
1553395 CIFC27 H46 O9P 21 21 216.9345; 13.2666; 28.7946
90; 90; 90
2649.02Sun, Na; Zhu, Yan; Zhou, Haofeng; Zhou, Junfei; Zhang, Hanqi; Zhang, Mengke; Zeng, Hong; Yao, Guangmin
Grayanane Diterpenoid Glucosides from the Leaves of Rhododendron micranthum and Their Bioactivities Evaluation.
Journal of natural products, 2018, 81, 2673-2681
1553396 CIFC26 H44 O10P 1 21 112.2958; 6.6149; 15.8066
90; 92.789; 90
1284.11Sun, Na; Zhu, Yan; Zhou, Haofeng; Zhou, Junfei; Zhang, Hanqi; Zhang, Mengke; Zeng, Hong; Yao, Guangmin
Grayanane Diterpenoid Glucosides from the Leaves of Rhododendron micranthum and Their Bioactivities Evaluation.
Journal of natural products, 2018, 81, 2673-2681
1553397 CIFC30 H42 O4P 21 21 219.209; 14.6102; 18.3937
90; 90; 90
2474.79Tabefam, Marzieh; Moridi Farimani, Mahdi; Danton, Ombeline; Ramseyer, Justine; Nejad Ebrahimi, Samad; Neuburger, Markus; Kaiser, Marcel; Salehi, Peyman; Potterat, Olivier; Hamburger, Matthias
Antiprotozoal Isoprenoids from Salvia hydrangea.
Journal of natural products, 2018, 81, 2682-2691
1553398 CIFC36 H48 O9P 1 21 114.1355; 18.3034; 20.5777
90; 97.024; 90
5284.1Kúsz, Norbert; Orvos, Péter; Bereczki, Laura; Fertey, Pierre; Bombicz, Petra; Csorba, Attila; Tálosi, László; Jakab, Gusztáv; Hohmann, Judit; Rédei, Dóra
Diterpenoids from Euphorbia dulcis with Potassium Ion Channel Inhibitory Activity with Selective G Protein-Activated Inwardly Rectifying Ion Channel (GIRK) Blocking Effect.
Journal of natural products, 2018, 81, 2483-2492
1553399 CIFC25 H28 O9P 32 2 111.686; 11.686; 29.8596
90; 90; 120
3531.4Arunrattiyakorn, Panarat; Kuno, Mayuso; Aree, Thammarat; Laphookhieo, Surat; Sriyatep, Teerayut; Kanzaki, Hiroshi; Garcia Chavez, Miguel Angel; Wang, Yan Alexander; Andersen, Raymond J.
Biotransformation of β-Mangostin by an Endophytic Fungus of Garcinia mangostana to Furnish Xanthenes with an Unprecedented Heterocyclic Skeleton.
Journal of natural products, 2018, 81, 2244-2250
1553400 CIFC25 H28 O9P 31 2 111.6878; 11.6878; 29.8747
90; 90; 120
3534.27Arunrattiyakorn, Panarat; Kuno, Mayuso; Aree, Thammarat; Laphookhieo, Surat; Sriyatep, Teerayut; Kanzaki, Hiroshi; Garcia Chavez, Miguel Angel; Wang, Yan Alexander; Andersen, Raymond J.
Biotransformation of β-Mangostin by an Endophytic Fungus of Garcinia mangostana to Furnish Xanthenes with an Unprecedented Heterocyclic Skeleton.
Journal of natural products, 2018, 81, 2244-2250
1553401 CIFC25 H28 O9C 1 2/c 122.1574; 10.8642; 21.0512
90; 115.067; 90
4590.2Arunrattiyakorn, Panarat; Kuno, Mayuso; Aree, Thammarat; Laphookhieo, Surat; Sriyatep, Teerayut; Kanzaki, Hiroshi; Garcia Chavez, Miguel Angel; Wang, Yan Alexander; Andersen, Raymond J.
Biotransformation of β-Mangostin by an Endophytic Fungus of Garcinia mangostana to Furnish Xanthenes with an Unprecedented Heterocyclic Skeleton.
Journal of natural products, 2018, 81, 2244-2250
1553402 CIFC21 H24 O8P 21 21 219.7873; 10.4684; 18.7272
90; 90; 90
1918.74Fragoso-Serrano, Mabel; Ortiz-Pastrana, Naytzé; Luna-Cruz, Norma; Toscano, Rubén A; Alpuche-Solís, Angel G; Ortega, Alfredo; Bautista, Elihú
Amarisolide F, an Acylated Diterpenoid Glucoside and Related Terpenoids from Salvia amarissima.
Journal of natural products, 2019, 82, 631-635
1553403 CIFC22 H22 O8P 21 21 216.9791; 12.6221; 22.9412
90; 90; 90
2020.91Fragoso-Serrano, Mabel; Ortiz-Pastrana, Naytzé; Luna-Cruz, Norma; Toscano, Rubén A; Alpuche-Solís, Angel G; Ortega, Alfredo; Bautista, Elihú
Amarisolide F, an Acylated Diterpenoid Glucoside and Related Terpenoids from Salvia amarissima.
Journal of natural products, 2019, 82, 631-635
1553404 CIFC41 H33 Cl N4 O11P -110.676; 12.903; 14.232
109.594; 94.193; 100.114
1799.8Pepe, Giulio; Cole, Jacqueline M.; Waddell, Paul G.; Perry, James I.
Rationalizing the suitability of rhodamines as chromophores in dye-sensitized solar cells: a systematic molecular design study
Molecular Systems Design & Engineering, 2016, 1, 416
1553405 CIFC27 H29 Cl N2 O7P -19.494; 11.509; 11.755
98.007; 99.366; 94.805
1247.5Pepe, Giulio; Cole, Jacqueline M.; Waddell, Paul G.; Perry, James I.
Rationalizing the suitability of rhodamines as chromophores in dye-sensitized solar cells: a systematic molecular design study
Molecular Systems Design & Engineering, 2016, 1, 416
1553406 CIFC34 H37 Cl N2 O8P 1 21/a 112.411; 21.348; 12.558
90; 117.284; 90
2957Pepe, Giulio; Cole, Jacqueline M.; Waddell, Paul G.; Perry, James I.
Rationalizing the suitability of rhodamines as chromophores in dye-sensitized solar cells: a systematic molecular design study
Molecular Systems Design & Engineering, 2016, 1, 416
1553407 CIFC42 H54 Cl4 N4 Ni2 O2P -19.7278; 10.55; 11.522
91.22; 109.68; 108.69
1043.6Zhang, Youfu; Huang, Chuanbing; Wang, Xinxin; Mahmood, Qaiser; Hao, Xiang; Hu, Xinquan; Guo, Cun-Yue; Solan, Gregory A.; Sun, Wen-Hua
Highly branched unsaturated polyethylenes achievable using strained imino-cyclopenta[b]pyridyl-nickel precatalysts
Polymer Chemistry, 2017, 8, 995
1553408 CIFC36 H40 Cl2 N4 NiP 1 21/n 19.0742; 14.496; 12.391
90; 98.03; 90
1613.9Zhang, Youfu; Huang, Chuanbing; Wang, Xinxin; Mahmood, Qaiser; Hao, Xiang; Hu, Xinquan; Guo, Cun-Yue; Solan, Gregory A.; Sun, Wen-Hua
Highly branched unsaturated polyethylenes achievable using strained imino-cyclopenta[b]pyridyl-nickel precatalysts
Polymer Chemistry, 2017, 8, 995
1553409 CIFC17 H20 Br N O5P -15.2286; 8.35; 20.2441
79.956; 89.888; 81.369
860.17Xie, Tongqing; Zhang, Baicheng; Zhang, Xuepeng; Zhang, Guoqing
AIE-active β-diketones containing pyridiniums: fluorogenic binding to cellulose and water-vapour-recoverable mechanochromic luminescence
Materials Chemistry Frontiers, 2017, 1, 693
1553410 CIFC46 H44 Br2 N2 NiC 1 2/c 19.6692; 15.1682; 28.4042
90; 95.927; 90
4143.61Sui, Xuelin; Hong, Changwen; Pang, Wenmin; Chen, Changle
Unsymmetrical α-diimine palladium catalysts and their properties in olefin (co)polymerization
Materials Chemistry Frontiers, 2017, 1, 967
1553411 CIFC56 H49 Cl3 N2 PdP 1 21/n 110.7748; 24.3601; 18.0013
90; 95.951; 90
4699.4Sui, Xuelin; Hong, Changwen; Pang, Wenmin; Chen, Changle
Unsymmetrical α-diimine palladium catalysts and their properties in olefin (co)polymerization
Materials Chemistry Frontiers, 2017, 1, 967
1553412 CIFC47 H47 Cl N2 PdP -113.1491; 19.2193; 19.3227
105.127; 109.315; 96.896
4333Sui, Xuelin; Hong, Changwen; Pang, Wenmin; Chen, Changle
Unsymmetrical α-diimine palladium catalysts and their properties in olefin (co)polymerization
Materials Chemistry Frontiers, 2017, 1, 967
1553413 CIFC28 H20 SI 1 2 115.4081; 6.0485; 22.1271
90; 102.299; 90
2014.83Nie, Han; Hu, Kun; Cai, Yuanjing; Peng, Qian; Zhao, Zujin; Hu, Rongrong; Chen, Junwu; Su, Shi-Jian; Qin, Anjun; Tang, Ben Zhong
Tetraphenylfuran: aggregation-induced emission or aggregation-caused quenching?
Materials Chemistry Frontiers, 2017, 1, 1125
1553414 CIFC28 H20 OI 1 2/c 121.71; 8.16; 24.855
90; 113.396; 90
4041Nie, Han; Hu, Kun; Cai, Yuanjing; Peng, Qian; Zhao, Zujin; Hu, Rongrong; Chen, Junwu; Su, Shi-Jian; Qin, Anjun; Tang, Ben Zhong
Tetraphenylfuran: aggregation-induced emission or aggregation-caused quenching?
Materials Chemistry Frontiers, 2017, 1, 1125
1553415 CIFC40 H26 N2 O2 S2P -110.495; 11.772; 13.789
81.56; 71.751; 72.938
1543.9Keshav, Karunesh; Kumawat, Mukesh Kumar; Srivastava, Rohit; Ravikanth, M.
Benzothiazoles-substituted tetraphenylethylenes: synthesis, structure, aggregation-induced emission and biological studies
Materials Chemistry Frontiers, 2017, 1, 1207
1553416 CIFC42 H30 N2 O2 S2P -113.352; 16.32; 17.943
99.33; 104.402; 108.992
3452.4Keshav, Karunesh; Kumawat, Mukesh Kumar; Srivastava, Rohit; Ravikanth, M.
Benzothiazoles-substituted tetraphenylethylenes: synthesis, structure, aggregation-induced emission and biological studies
Materials Chemistry Frontiers, 2017, 1, 1207
1553417 CIFC78 H82 N4 O16 Zn3P -111.4427; 14.514; 16.196
65.694; 69.783; 73.998
2272.2King, Stephen Charles; Lin, Rui-Biao; Wang, Hailong; Arman, Hadi D.; Chen, Banglin
Two-dimensional metal‒organic frameworks for selective separation of CO2/CH4 and CO2/N2
Materials Chemistry Frontiers, 2017, 1, 1514
1553418 CIFC21 H15 Br F N OP -15.9396; 11.302; 13.413
96.05; 99.59; 101.21
862Sheng, Jinyu; Su, Xiang; Cao, Chengyao; Chen, Chao
Synthesis of benzo[1,3]oxazines via copper(i)-catalyzed cascade annulation of nitriles, aldehydes and diaryliodonium salts
Organic Chemistry Frontiers, 2016, 3, 501
1553419 CIFC28 H22 F3 N O5P 21 21 219.1158; 9.8126; 28.3116
90; 90; 90
2532.46Gao, Tai-Ping; Liu, Dan; Lin, Jun-Bing; Hu, Xiu-Qin; Wang, Zhu-Yin; Xu, Peng-Fei
Direct construction of chiral quaternary dihydropyranones through highly enantioselective organocatalytic hetero-Diels–Alder reactions of olefinic azlactones
Organic Chemistry Frontiers, 2016, 3, 598
1553420 CIFC25 H48 N2 O5 S SiP 1 21 112.5809; 8.9728; 13.319
90; 93.554; 90
1500.64Ye, Jian-Liang; Chen, Hang; Zhang, Yu-Feng; Huang, Pei-Qiang
A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline
Organic Chemistry Frontiers, 2016, 3, 683
1553421 CIFC20 H28 Cl N2 O4.5 SP 21 21 2111.701; 14.628; 25.939
90; 90; 90
4439.8Ye, Jian-Liang; Chen, Hang; Zhang, Yu-Feng; Huang, Pei-Qiang
A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline
Organic Chemistry Frontiers, 2016, 3, 683
1553422 CIFC250 H238 F24 N18 O12 P4 Ru2P n n n :222.824; 22.583; 47.813
90; 90; 90
24644.5Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553423 CIFC90 H102 F12 N10 O8 P2 RuP 1 21/n 120.3614; 15.5902; 30.5936
90; 94.4504; 90
9682.3Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553424 CIFC102 H130 F12 N10 O26 S4 Zn2P -111.0301; 12.3939; 21.8715
76.878; 78.788; 87.305
2856.3Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553425 CIFC155 H166 Cl22 F24 N12 O12 P4 Ru2P -115.004; 15.1525; 21.5611
98.4023; 98.0121; 108.321
4512.9Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553426 CIFC98 H98 Br2 F12 N16 O10 P2 RuP 1 21/n 114.556; 24.668; 26.949
90; 93.27; 90
9660.8Veliks, Janis; Seifert, Helen M.; Frantz, Derik K.; Klosterman, Jeremy K.; Tseng, Jui-Chang; Linden, Anthony; Siegel, Jay S.
Towards the molecular Borromean link with three unequal rings: double-threaded ruthenium(ii) ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 667
1553427 CIFC180 H194 F24 N22 O18 P4 Ru2P -113.6711; 16.967; 22.4266
71.073; 82.622; 68.288
4571.45Veliks, Janis; Seifert, Helen M.; Frantz, Derik K.; Klosterman, Jeremy K.; Tseng, Jui-Chang; Linden, Anthony; Siegel, Jay S.
Towards the molecular Borromean link with three unequal rings: double-threaded ruthenium(ii) ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 667
1553428 CIFC14 H16 O5P 1 21/c 119.5895; 7.0388; 9.2405
90; 91.626; 90
1273.63Yu, Jingxun; Ma, Haichen; Yao, Hongliang; Cheng, Hang; Tong, Rongbiao
Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2016, 3, 714
1553429 CIFC14 H16 O5P 1 21/c 18.144; 14.5913; 11.013
90; 94.901; 90
1303.91Yu, Jingxun; Ma, Haichen; Yao, Hongliang; Cheng, Hang; Tong, Rongbiao
Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2016, 3, 714
1553430 CIFC17 H16 Cl N O2P 21 21 218.1449; 10.8999; 16.4545
90; 90; 90
1460.81Vyas, Vijyesh K.; Bhanage, Bhalchandra M.
Asymmetric transfer hydrogenation of seven membered tricyclic ketones: N-substituted dibenzo[b,e]azepine-6,11-dione driven by nonclassical CH/O interactions
Organic Chemistry Frontiers, 2016, 3, 614
1553431 CIFC31 H28 N4 O3P 1 21 19.837; 10.113; 14.456
90; 106.063; 90
1382Zhu, Yi; Li, Yao; Meng, Qingbin; Li, Xin
An organocatalytic enantioselective vinylogous Mannich reaction of α,α-dicyanoolefins with isatin N-Boc ketimines
Organic Chemistry Frontiers, 2016, 3, 709
1553432 CIFC23 H15 Cl3 N2 O2P c a 217.7032; 16.441; 14.9629
90; 90; 90
1895Zhang, Zeyuan; Dai, Zhen; Ma, Xinkun; Liu, Yihan; Ma, Xiaojun; Li, Wanli; Ma, Chen
Cu-catalyzed one-pot synthesis of fused oxazepinone derivatives via sp2 C–H and O–H cross-dehydrogenative coupling
Organic Chemistry Frontiers, 2016, 3, 799
1553433 CIFC21 H12 Cl N3 O2P -17.147; 7.9449; 16.405
101.767; 96.018; 106.731
859.9Zhang, Zeyuan; Dai, Zhen; Ma, Xinkun; Liu, Yihan; Ma, Xiaojun; Li, Wanli; Ma, Chen
Cu-catalyzed one-pot synthesis of fused oxazepinone derivatives via sp2 C–H and O–H cross-dehydrogenative coupling
Organic Chemistry Frontiers, 2016, 3, 799
1553434 CIFC16 H11 Br O2P 1 21/c 19.986; 15.521; 8.74
90; 101.027; 90
1329.6Qiu, Guanyinsheng; Liu, Tong; Ding, Qiuping
Tandem oxidative radical brominative addition of activated alkynes and spirocyclization: switchable synthesis of 3-bromocoumarins and 3-bromo spiro-[4,5] trienone
Organic Chemistry Frontiers, 2016, 3, 510
1553435 CIFC37 H24 O3P -16.3266; 11.3868; 18.6894
94.305; 99.144; 100.166
1301Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553436 CIFC37 H26 O2P -16.514; 11.9444; 17.215
93.28; 94.949; 104.241
1289.2Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553437 CIFC38 H27 N O3.5P -112.8713; 12.9061; 18.4438
83.491; 70.221; 87.197
2864.3Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553438 CIFC41 H34 O6P 1 21/c 19.5936; 9.4163; 34.688
90; 93.15; 90
3128.8Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553439 CIFC38 H26 O2P -19.837; 10.766; 13.71
87.68; 77.4; 71.54
1343.4Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553440 CIFC29 H20 OC 1 2/c 126.128; 8.1552; 21.487
90; 119.724; 90
3976Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553441 CIFC71 H64 O24P 1 21/c 119.7803; 8.925; 17.1219
90; 93.062; 90
3018.37Leowanawat, Pawaret; Nowak-Król, Agnieszka; Würthner, Frank
Tetramethoxy-bay-substituted perylene bisimides by copper-mediated cross-coupling
Organic Chemistry Frontiers, 2016, 3, 537
1553442 CIFC20 H24 N2P 1 21/n 113.1094; 8.943; 14.6031
90; 105.214; 90
1652.03Peng, Xingao; Kaga, Atsushi; Hirao, Hajime; Chiba, Shunsuke
Hydroamination of alkenyl N-arylhydrazones mediated by t-BuOK for the synthesis of nitrogen heterocycles
Organic Chemistry Frontiers, 2016, 3, 609
1553443 CIFC23 H24 N2 SP 1 21/n 111.6939; 9.4598; 16.9069
90; 91.481; 90
1869.65Peng, Xingao; Kaga, Atsushi; Hirao, Hajime; Chiba, Shunsuke
Hydroamination of alkenyl N-arylhydrazones mediated by t-BuOK for the synthesis of nitrogen heterocycles
Organic Chemistry Frontiers, 2016, 3, 609
1553444 CIFC16 H16 O3 SP 21 21 215.9262; 8.0475; 31.957
90; 90; 90
1524.06Phanindrudu, Mandalaparthi; Tiwari, Dipak Kumar; Sridhar, B.; Likhar, Pravin R.; Tiwari, Dharmendra Kumar
Magnetically separable nano-copper catalyzed unprecedented stereoselective synthesis of E-vinyl sulfones from tosylmethyl isocyanide and alkynes: TosMIC as a source of the sulfonyl group
Organic Chemistry Frontiers, 2016, 3, 795
1553445 CIFC23 H20 Br2 N2 O2P 1 21/n 113.4028; 11.2931; 14.0439
90; 91.99; 90
2124.4Hu, Haoxiang; Wang, Yidong; Qian, Deyun; Zhang, Zhan-Ming; Liu, Lu; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2 + 2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone
Organic Chemistry Frontiers, 2016, 3, 759
1553446 CIFC36 H56 Au Cl N O P SP 1 21 112.5457; 22.382; 12.6621
90; 92.052; 90
3553.2Hu, Haoxiang; Wang, Yidong; Qian, Deyun; Zhang, Zhan-Ming; Liu, Lu; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2 + 2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone
Organic Chemistry Frontiers, 2016, 3, 759
1553447 CIFC26 H21 N O3 SC 1 2/c 121.51; 10.73; 19.7
90; 113.492; 90
4170Gong, Xinxing; Xia, Hongguang; Wu, Jie
A palladium-catalyzed tandem reaction of 2-alkynylbenzenesulfonamides with 2-(2-bromoarylidene)cyclobutanones
Organic Chemistry Frontiers, 2016, 3, 697
1553448 CIFC23 H21 F N4P -110.5273; 11.4221; 34.217
90.072; 98.137; 105.697
3917.7Jiang, Yu; Wang, Qiang; Sun, Run; Tang, Xiang-Ying; Shi, Min
Base-induced synthesis of N-dialkylaminomethyl-2H-1,2,3-triazoles from N-sulfonyl-1,2,3-triazoles
Organic Chemistry Frontiers, 2016, 3, 744
1553449 CIFC32 H25 N O6P 21 21 219.02156; 9.44417; 30.948
90; 90; 90
2636.81Ran, Guang-Yao; Wang, Pan; Du, Wei; Chen, Ying-Chun
α-Regioselective [3 + 2] annulations with Morita‒Baylis‒Hillman carbonates of isatins and 2-nitro-1,3-enynes
Organic Chemistry Frontiers, 2016, 3, 861
1553450 CIFC21 H13 N SP -17.187; 10.356; 11.075
66.214; 86.273; 89.284
752.6Wen, Li-Rong; Shen, Qiang-Yu; Guo, Wei-Si; Li, Ming
Copper-catalyzed tandem arylation–cyclization of 2-alkynylaryl isothiocyanates with diaryliodonium salts: an efficient synthesis of thiochromeno[2,3-b]indoles
Organic Chemistry Frontiers, 2016, 3, 870
1553451 CIFC22 H17 N O2 SP -111.0789; 11.6353; 16.29
93.084; 106.29; 115.259
1786.1Wen, Li-Rong; Shen, Qiang-Yu; Guo, Wei-Si; Li, Ming
Copper-catalyzed tandem arylation–cyclization of 2-alkynylaryl isothiocyanates with diaryliodonium salts: an efficient synthesis of thiochromeno[2,3-b]indoles
Organic Chemistry Frontiers, 2016, 3, 870
1553452 CIFC19 H17 N O5P 1 21/n 113.5013; 18.6052; 13.6121
90; 106.649; 90
3275.9Görgen née Boersch, Christina; Lutsenko, Kiril; Merkul, Eugen; Frank, Walter; Müller, Thomas J. J.
Catalytic one-pot synthesis of 4-(hetero)aryl substituted 5-(2-oxoethyl) oxazol-2(3H)-ones by coupling–isomerization–elimination (CIE) sequence
Organic Chemistry Frontiers, 2016, 3, 887
1553453 CIFC48 H53 Cl2 N3 O6 Ru SP 1 21/c 18.4973; 40.566; 26.516
90; 97.469; 90
9063Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553454 CIFC44 H49 Cl2 N3 O3 Ru SP n a 2116.8326; 12.2762; 20.4575
90; 90; 90
4227.3Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553455 CIFC40 H47 Cl2 N3 O4 Ru SP 1 21/c 111.3136; 21.889; 16.102
90; 97.063; 90
3957.3Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553456 CIFC36 H46 Cl2 N2 O3 RuP 1 21/c 120.114; 8.8782; 20.665
90; 105.736; 90
3552Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553457 CIFC22 H26 Cl3 N2 O RuP 21 21 212.073; 18.008; 10.7084
90; 90; 90
2328.1Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553458 CIFC42 H43 Cl2 N3 O4 Ru SR -3 :H40.354; 40.354; 14.657
90; 90; 120
20670Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553459 CIFC14 H10 F12 N2P 1 21/n 110.0639; 8.163; 20.469
90; 101.995; 90
1644.8Xie, Jin; Li, Jian; Wurm, Thomas; Weingand, Vanessa; Sung, Hui-Ling; Rominger, Frank; Rudolph, Matthias; Hashmi, A. Stephen K.
A general photoinduced electron transfer-directed chemoselective perfluoroalkylation of N,N-dialkylhydrazones
Organic Chemistry Frontiers, 2016, 3, 841
1553460 CIFC27 H26 Cl2 F3 N7 SP b c a16.558; 17.307; 19.571
90; 90; 90
5608Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang
Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates
Organic Chemistry Frontiers, 2016, 3, 880
1553461 CIFC27 H23 F6 N7 S2P -19.817; 11.968; 13.149
102.73; 99.17; 104.43
1421.3Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang
Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates
Organic Chemistry Frontiers, 2016, 3, 880
1553462 CIFC27 H23 F6 N7 S2P 1 21/c 114.717; 15.564; 12.282
90; 103.48; 90
2735.8Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang
Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates
Organic Chemistry Frontiers, 2016, 3, 880
1553463 CIFC17 H25 Cl2 N3 O4 SP -110.82; 10.975; 11.163
74.634; 62.808; 65.132
1065.4Zhou, Kaida; Xia, Hongguang; Wu, Jie
Generation of (2-oxoindolin-3-yl)methanesulfonohydrazides via a photo-induced reaction of N-(2-iodoaryl)acrylamide, DABSO, and hydrazine
Organic Chemistry Frontiers, 2016, 3, 865
1553464 CIFC22 H18 F3 N O6P -111.266; 12.1474; 16.278
73.095; 73.52; 84.96
2043.8Li, Zong-Rui; Bao, Xing-Xing; Sun, Jian; Shen, Jing; Wu, Dun-Qi; Liu, Yan-Kai; Deng, Qing-Hai; Liu, Feng
Iron-catalyzed trifluoromethylation of vinylcyclopropanes: facile synthesis of CF3–containing dihydronaphthalene derivatives
Organic Chemistry Frontiers, 2016, 3, 934
1553465 CIFC16 H16 B N3 O2I 1 2/a 125.856; 5.37038; 21.5154
90; 101.646; 90
2926.05Zhai, Wenlei; Chapin, Brette M.; Yoshizawa, Akina; Wang, Hui-Chen; Hodge, Stephen A.; James, Tony D.; Anslyn, Eric V.; Fossey, John S.
“Click-fluors”: triazole-linked saccharide sensors
Organic Chemistry Frontiers, 2016, 3, 918
1553466 CIFC24 H24 B N3 O4P -17.1065; 9.0913; 17.685
81.994; 84.409; 68.79
1053.43Zhai, Wenlei; Chapin, Brette M.; Yoshizawa, Akina; Wang, Hui-Chen; Hodge, Stephen A.; James, Tony D.; Anslyn, Eric V.; Fossey, John S.
“Click-fluors”: triazole-linked saccharide sensors
Organic Chemistry Frontiers, 2016, 3, 918
1553467 CIFC14 H10 Br N O2P 21 21 214.4197; 11.6677; 22.915
90; 90; 90
1181.7Zhang, Xu; Xu, Bin; Xu, Ming-Hua
Rhodium-catalyzed asymmetric arylation of N- and O-containing cyclic aldimines: facile and efficient access to highly optically active 3,4-dihydrobenzo[1,4]oxazin-2-ones and dihydroquinoxalinones
Organic Chemistry Frontiers, 2016, 3, 944
1553468 CIFC14 H15 Cl N2 PdP 1 c 19.4647; 12.7252; 11.5908
90; 108.624; 90
1322.9Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553469 CIFC16 H19 Cl N2 PdP 1 21/c 19.6575; 11.675; 26.2578
90; 92.079; 90
2958.7Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553470 CIFC16 H17 Cl N2 O PdP 1 21/n 16.9704; 17.1706; 12.2014
90; 97.943; 90
1446.33Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553471 CIFC24 H19 Cl N O P PdP 1 21/n 112.2558; 9.9099; 17.4367
90; 109.768; 90
1992.95Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553472 CIFC23 H17 Cl N O P PdP -19.0641; 9.6782; 12.7031
91.535; 108.207; 112.231
966.47Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553473 CIFC25 H17 N O SP 1 21/n 15.4373; 22.5643; 15.678
90; 91.295; 90
1923Singh, Radhey M.; Kumar, Ritush; Bharadwaj, Kishor Chandra; Gupta, Tanu
Pd catalyzed facile synthesis of cyclopenta[b]quinolin-1-one via sequential Sonogashira coupling and annulation. An unusual mode of ring closure, using sulphur as a soft nucleophile
Organic Chemistry Frontiers, 2016, 3, 1100
1553474 CIFC36 H26P -19.2253; 12.0172; 12.8207
65.023; 76.245; 83.655
1251.4He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553475 CIFC32 H24P 1 21/n 19.4248; 9.6366; 25.0543
90; 94.474; 90
2268.6He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553476 CIFC40 H28P 1 21/c 116.4844; 9.1722; 19.225
90; 107.472; 90
2772.7He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553477 CIFC40 H28P 1 21/n 111.3717; 15.9519; 15.1309
90; 93.429; 90
2739.83He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553478 CIFC42 H28P 1 21/c 19.5798; 10.2198; 29.4004
90; 96.324; 90
2860.89He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553479 CIFC28 H23 Cl N4 O7P 1 21 112.766; 16.24; 13.427
90; 107.96; 90
2648Li, Jun-Hua; Cui, Zhi-Hao; Du, Da-Ming
Diastereo- and enantioselective construction of cyclohexanone-fused spirospyrazolones containing four consecutive stereocenters through asymmetric sequential reactions
Organic Chemistry Frontiers, 2016, 3, 1087
1553480 CIFC17 H22 O2P 1 21/c 111.7876; 19.8876; 12.1607
90; 94.193; 90
2843.2Ondet, Pierrick; Lempenauer, Luisa; Duñach, Elisabet; Lemière, Gilles
Bismuth(iii) triflate-catalysed tandem cyclisations towards complex polycyclic ethers
Organic Chemistry Frontiers, 2016, 3, 999
1553481 CIFC17 H22 O2P 1 21/c 119.1606; 13.3348; 23.8068
90; 108.315; 90
5774.6Ondet, Pierrick; Lempenauer, Luisa; Duñach, Elisabet; Lemière, Gilles
Bismuth(iii) triflate-catalysed tandem cyclisations towards complex polycyclic ethers
Organic Chemistry Frontiers, 2016, 3, 999
1553482 CIFC23 H27 N O6 SP 1 21/n 18.2306; 9.8924; 26.999
90; 98.152; 90
2176.1Duan, Shuangshuang; Long, Dan; Zhao, Changgui; Zhao, Gaoyuan; Yuan, Ziyun; Xie, Xingang; Fang, Jianguo; She, Xuegong
Efficient construction of the A/C/D tricyclic skeleton of palhinine A
Organic Chemistry Frontiers, 2016, 3, 1137
1553483 CIFC23 H19 Br OP 1 21/n 110.005; 9.977; 18.125
90; 92.34; 90
1807.7Liu, Yu; Zhao, Peng; Zhang, Bo; Xi, Chanjuan
MeOTf-catalyzed annulation of aldehydes and arylalkynes leading to 2,3-disubstituted indanones
Organic Chemistry Frontiers, 2016, 3, 1116
1553484 CIFC23 H20 SP -19.756; 10.716; 10.881
65.921; 68.07; 63.361
902.7Ramesh, E.; Shankar, Majji; Dana, Suman; Sahoo, Akhila K.
Silver-mediated oxidative annulation of N-arylthio succinimides with alkynes: direct access to benzo[b]thiophenes
Organic Chemistry Frontiers, 2016, 3, 1126
1553485 CIFC20 H13 F SP 1 21/c 16.0606; 13.4845; 18.39
90; 91.36; 90
1502.5Ramesh, E.; Shankar, Majji; Dana, Suman; Sahoo, Akhila K.
Silver-mediated oxidative annulation of N-arylthio succinimides with alkynes: direct access to benzo[b]thiophenes
Organic Chemistry Frontiers, 2016, 3, 1126
1553486 CIFC20 H17 F3 I N OC 1 2/c 131.8; 8.994; 13.605
90; 110.595; 90
3642An, Yuanyuan; Kuang, Yunyan; Wu, Jie
Synthesis of trifluoromethylated 3,4-dihydroquinolin-2(1H)-ones via a photo-induced radical cyclization of benzene-tethered 1,7-enynes with Togni reagent
Organic Chemistry Frontiers, 2016, 3, 994
1553487 CIFC21 H19 Br N2 O4P 21 21 218.4058; 10.8659; 21.9188
90; 90; 90
2001.99Ma, Qiao; Gong, Lei; Meggers, Eric
Enantioselective β-alkylation of pyrroles with the formation of an all-carbon quaternary stereocenter
Organic Chemistry Frontiers, 2016, 3, 1319
1553488 CIFC20 H18 N6 OP 1 21/c 120.5231; 9.5667; 20.3255
90; 115.091; 90
3614.1Liu, Hou-Lu; Jiang, Yu; Hao, Jian; Tang, Xiang-Ying; Shi, Min
A new method to access triazole-fused spiro-guanidines from the reaction of isothiocyanates tethered N-sulfonyl-1,2,3-triazoles and amines
Organic Chemistry Frontiers, 2016, 3, 1447
1553489 CIFC18 H11 I N2 OP -17.504; 8.467; 13.179
95.607; 102.6; 110.95
748.8Wu, Yan-Dong; Geng, Xiao; Gao, Qinghe; Zhang, Jingjing; Wu, Xia; Wu, An-Xin
Iodine-promoted sequential dual oxidative Csp3–H amination/Csp3–H iodination reactions: efficient synthesis of 1-iodoimidazo[1,5-a]pyridines
Organic Chemistry Frontiers, 2016, 3, 1430
1553490 CIFC60 H44 N4 O4 Pd2P c c n20.2007; 25.2676; 31.3498
90; 90; 90
16001.7Naito, Masaya; Komiya, Naruyoshi; Naota, Takeshi
Homochiral association of binuclear trans-bis(β-iminoaryloxy)palladium(ii) complexes doubly linked with m-xylylene spacers: drastic linker-dependence of the association chirality of chiral clothespin-shaped molecules
Organic Chemistry Frontiers, 2016, 3, 1286
1553491 CIFC61 H45 Cl3 N4 O4 Pd2C 1 2/c 127.6181; 13.0551; 30.802
90; 113.65; 90
10173.2Naito, Masaya; Komiya, Naruyoshi; Naota, Takeshi
Homochiral association of binuclear trans-bis(β-iminoaryloxy)palladium(ii) complexes doubly linked with m-xylylene spacers: drastic linker-dependence of the association chirality of chiral clothespin-shaped molecules
Organic Chemistry Frontiers, 2016, 3, 1286
1553492 CIFC29 H44 O6 SiP 21 21 2111.5223; 14.9948; 16.4141
90; 90; 90
2835.9Pérez-Estrada, S.; Sayar, N.; Granja, J. R.
Towards taxane analogues synthesis by dienyne ring closing metathesis
Organic Chemistry Frontiers, 2016, 3, 1331
1553493 CIFC29 H40 O5 SiC 1 2 127.836; 7.8125; 14.1759
90; 92.711; 90
3079.4Pérez-Estrada, S.; Sayar, N.; Granja, J. R.
Towards taxane analogues synthesis by dienyne ring closing metathesis
Organic Chemistry Frontiers, 2016, 3, 1331
1553494 CIFC17 H14 O2P 1 21/c 113.6594; 5.9624; 17.4715
90; 106.688; 90
1363Cui, Fei-Hu; Su, Shi-Xia; Xu, Yan-li; Liang, Ying; Wang, Heng-shan; Pan, Ying-Ming
Capture of CO2 in air for 4,5-disubstituted furan-2(5H)-ones
Organic Chemistry Frontiers, 2016, 3, 1304
1553495 CIFC38 H24 Cl2 N2 O6P 1 21/c 114.2296; 6.2823; 33.8457
90; 90.358; 90
3025.56Wirtanen, T.; Muuronen, M.; Hurmalainen, J.; Tuononen, H. M.; Nieger, M.; Helaja, J.
Intermolecular oxidative dehydrogenative 3,3′-coupling of benzo[b]furans and benzo[b]thiophenes promoted by DDQ/H+: total synthesis of shandougenine B
Organic Chemistry Frontiers, 2016, 3, 1738
1553496 CIFC62 H61 N7 O20 S4P 1 21/n 113.909; 20.264; 22.762
90; 91.41; 90
6414Gaeta, Carmine; Della Sala, Paolo; Talotta, Carmen; De Rosa, Margherita; Soriente, Annunziata; Brancatelli, Giovanna; Geremia, Silvano; Neri, Placido
A tetrasulfate-resorcin[6]arene cavitand as the host for organic ammonium guests
Organic Chemistry Frontiers, 2016, 3, 1276
1553497 CIFC19 H17 N O4P -18.125; 9.328; 11.408
90.91; 96.19; 107.69
817.8Dai, Jie; Ren, Wenlong; Chang, Wenju; Zhang, Ping; Shi, Yian
An effective route to β2-amino acid derivatives via Pd-catalyzed regioselective hydrocarboxylation of 1,2-disubstituted enimides
Organic Chemistry Frontiers, 2017, 4, 297
1553498 CIFC14 H17 N5 O4P 21 21 217.51038; 17.3551; 23.2172
90; 90; 90
3026.21Naik, Siddhi D.; Chandra, Girish; Sahu, Pramod K.; Kim, Hong-Rae; Qu, Shuhao; Yoon, Ji-seong; Jeong, Lak Shin
Stereo- and regio-selective synthesis of 3′-C-substituted-(N)-methanocarba adenosines as potential anticancer agents
Organic Chemistry Frontiers, 2016, 3, 1472
1553499 CIFC16 H12 F3 N O2P 1 21/c 112.057; 8.771; 14.736
90; 113.287; 90
1431.4Mizuta, Satoshi; Otaki, Hiroki; Kitamura, Kanami; Nishi, Kodai; Watanabe, Ken; Makau, Juliann Nzembi; Hashimoto, Ryo; Usui, Toshiya; Chiba, Kenya
3,3-Dibromo-2-trifluoromethyl acrylic acid ethyl ester: a versatile platform for the stereoselective preparation of functionalized-α-trifluoromethyl α,β-unsaturated lactones and trifluoromethyl pyrazolinones
Organic Chemistry Frontiers, 2016, 3, 1661
1553500 CIFC17 H10 Cl F3 N2 OP -18.165; 9.432; 10.126
85.485; 83.241; 73.145
740.3Jin, Li-Kun; Lu, Guo-Ping; Cai, Chun
Copper-catalyzed 8-amido chelation-induced regioselective C–H fluoroalkylation of quinolines
Organic Chemistry Frontiers, 2016, 3, 1309
1553501 CIFC24 H15 NP 21 21 214.8217; 10.1093; 31.14
90; 90; 90
1517.89Zagranyarski, Yulian; Skabeev, Artem; Ma, Yingjie; Müllen, Klaus; Li, Chen
Facile synthesis of annulated heterocyclic benzo[kl]acridine derivatives via one-pot N–H/C–H coupling
Organic Chemistry Frontiers, 2016, 3, 1520
1553502 CIFC22 H13 N SP c a 2116.3471; 11.2916; 8.0242
90; 90; 90
1481.15Zagranyarski, Yulian; Skabeev, Artem; Ma, Yingjie; Müllen, Klaus; Li, Chen
Facile synthesis of annulated heterocyclic benzo[kl]acridine derivatives via one-pot N–H/C–H coupling
Organic Chemistry Frontiers, 2016, 3, 1520
1553503 CIFC23 H24 N2P -16.202; 10.169; 14.7158
75.057; 85.343; 84.132
890.56Liu, Cheng-Guo; Gu, Zheng-Yang; Bai, Hui-Wen; Wang, Shun-Yi; Ji, Shun-Jun
An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions
Organic Chemistry Frontiers, 2016, 3, 1299
1553504 CIFC22 H25 N2 O4 PP -18.9115; 11.1099; 11.8272
83.858; 86.228; 67.922
1078.45Sun, Mengmeng; Sun, Suyan; Qiao, Huijie; Yang, Fan; Zhu, Yu; Kang, Jianxun; Wu, Yusheng; Wu, Yangjie
Silver(i)-promoted C5–H phosphonation of 8-aminoquinoline amides with H-phosphonates
Organic Chemistry Frontiers, 2016, 3, 1646
1553505 CIFC22 H25 N2 O4 PP c c n15.3031; 18.1046; 15.6855
90; 90; 90
4345.8Sun, Mengmeng; Sun, Suyan; Qiao, Huijie; Yang, Fan; Zhu, Yu; Kang, Jianxun; Wu, Yusheng; Wu, Yangjie
Silver(i)-promoted C5–H phosphonation of 8-aminoquinoline amides with H-phosphonates
Organic Chemistry Frontiers, 2016, 3, 1646
1553506 CIFC31 H27 N2 O2P 21 21 218.681; 17.323; 32.77
90; 90; 90
4928Chen, Zhen; Huo, Yuwen; An, Ping; Wang, Xichao; Song, Chun; Ma, Yudao
[2.2]Paracyclophane-based N-heterocyclic carbene as efficient catalyst or as ligand for copper catalyst for asymmetric α-silylation of N-tosylaldimines
Organic Chemistry Frontiers, 2016, 3, 1725
1553507 CIFC17 H31 N O4P 21 21 217.643; 16.144; 6.601
90; 90; 90
1880.2Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553508 CIFC17 H31 N O4P 21 21 216.03; 16.334; 18.224
90; 90; 90
1795Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553509 CIFC13 H21 N O3P 1 21 110.178; 21.78; 11.615
90; 90.547; 90
2574.7Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553510 CIFC13 H21 N O3P 21 21 216.078; 10.204; 19.957
90; 90; 90
1237.73Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553511 CIFC26 H42 N2 O6P 1 21 17.252; 25.57; 14.465
90; 100.17; 90
2640.2Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553512 CIFC41 H31 Cl2 N O2P -19.1392; 13.2716; 13.7699
77.608; 76.026; 84.909
1581.79Seifert, Sabine; Schmidt, David; Würthner, Frank
A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides
Organic Chemistry Frontiers, 2016, 3, 1435
1553513 CIFC79 H66 Cl2 N2 O4P 1 21/c 113.3641; 15.796; 14.8901
90; 112.839; 90
2896.9Seifert, Sabine; Schmidt, David; Würthner, Frank
A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides
Organic Chemistry Frontiers, 2016, 3, 1435
1553514 CIFC24 H20 O2 SP 1 21/n 19.2961; 10.1519; 20.823
90; 102.267; 90
1920.26Fu, Rong; Hao, Wen-Juan; Wu, Ya-Nan; Wang, Nan-Nan; Tu, Shu-Jiang; Li, Guigen; Jiang, Bo
Sulfonyl radical-enabled 6-endo-trig cyclization for regiospecific synthesis of unsymmetrical diaryl sulfones
Organic Chemistry Frontiers, 2016, 3, 1452
1553515 CIFC27 H20 O2 SP 1 21/c 17.0521; 28.03; 10.4649
90; 100.069; 90
2036.7Fu, Rong; Hao, Wen-Juan; Wu, Ya-Nan; Wang, Nan-Nan; Tu, Shu-Jiang; Li, Guigen; Jiang, Bo
Sulfonyl radical-enabled 6-endo-trig cyclization for regiospecific synthesis of unsymmetrical diaryl sulfones
Organic Chemistry Frontiers, 2016, 3, 1452
1553516 CIFC33 H35 N O4 SP 1 21/c 115.4186; 11.3388; 16.9081
90; 107.55; 90
2818.4Lv, Leiyang; Bai, Xiaohui; Yan, Xiaoyu; Li, Zhiping
Iron-catalyzed decarbonylation initiated [2 + 2 + m] annulation of benzene-linked 1,n-enynes with aliphatic aldehydes
Organic Chemistry Frontiers, 2016, 3, 1509
1553517 CIFC29 H26 N2 O5 SP -18.3151; 8.625; 18.7838
99.74; 96.686; 104.017
1270.61Sharma, Pankaj; Kumar, Niggula Praveen; Krishna, Namballa Hari; Prasanna, Daasi; Sridhar, Balasubramanian; Shankaraiah, Nagula
Silver(i)-catalysed domino alkyne-annulation/Diels–Alder reaction: a mild synthetic approach to tetrahydrospiro[carbazole-4,3′-indoline] scaffolds
Organic Chemistry Frontiers, 2016, 3, 1503
1553518 CIFC14 H17 F3 N2 O3 SP 1 21/n 18.849; 10.773; 17.758
90; 91.599; 90
1692.2Li, Yuewen; Xiang, Yuanchao; Li, Zhiming; Wu, Jie
Direct vicinal difunctionalization of alkynes through trifluoromethylation and aminosulfonylation via insertion of sulfur dioxide under catalyst-free conditions
Organic Chemistry Frontiers, 2016, 3, 1493
1553519 CIFC36 H32 F2 N2 O2P 21 21 2111.5593; 14.0068; 17.8914
90; 90; 90
2896.78Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng
Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles
Organic Chemistry Frontiers, 2017, 4, 57
1553520 CIFC44 H50 N2P 1 21/c 119.661; 10.71; 17.118
90; 97.306; 90
3575Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng
Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles
Organic Chemistry Frontiers, 2017, 4, 57
1553521 CIFC16 H18 O3 SP -16.9478; 9.1969; 11.8012
82.206; 81.643; 75.22
717.55Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553522 CIFC15 H16 O2 SP 1 21/n 17.68603; 23.9176; 7.76261
90; 111.053; 90
1331.76Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553523 CIFC14 H11 N SP 1 21/n 15.7042; 25.743; 7.8069
90; 94.59; 90
1142.71Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553524 CIFC15 H14 O SP 1 21/n 15.7958; 25.4544; 8.3123
90; 93.626; 90
1223.85Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553525 CIFC15 H14 O2 SP 1 21/n 15.611; 25.6833; 8.991
90; 98.982; 90
1279.8Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553526 CIFC14 H11 N O SP 1 21/n 15.67633; 26.8781; 7.7875
90; 95.042; 90
1183.53Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553527 CIFC14 H8 N2 S2P -17.8232; 11.6428; 14.5818
84.863; 83.654; 73.557
1263.68Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553528 CIFC22 H32 O2 SiP b c a12.7034; 11.6077; 28.683
90; 90; 90
4229.5Liu, Zhen; Xia, Ying; Feng, Sheng; Zhang, Yan; Wang, Jianbo
Rh(i)-Catalyzed coupling of 2-bromoethyl aryldiazoacetates with tertiary propargyl alcohols through carbene migratory insertion
Organic Chemistry Frontiers, 2016, 3, 1691
1553529 CIFC24 H19 N O3P -19.3034; 9.6541; 11.6687
101.875; 106.962; 96.397
964.39Duan, Jindian; Cheng, Yuyu; Li, Rou; Li, Pengfei
Synthesis of spiro[indane-1,3-dione-1-pyrrolines] via copper-catalyzed heteroannulation of ketoxime acetates with 2-arylideneindane-1,3-diones
Organic Chemistry Frontiers, 2016, 3, 1614
1553530 CIFC35 H53 N O3P 1 21 17.455; 11.3624; 18.4877
90; 92.585; 90
1564.44Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing
A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum
Organic Chemistry Frontiers, 2017, 4, 42
1553531 CIFC30 H50 O3P 21 21 216.52391; 12.9427; 31.7963
90; 90; 90
2684.78Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing
A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum
Organic Chemistry Frontiers, 2017, 4, 42
1553532 CIFC18 H16 O SP b c a11.1348; 10.8734; 24.741
90; 90; 90
2995.5An, Zhenyu; She, Yue; Yang, Xiaodong; Pang, Xiaobo; Yan, Rulong
Metal-free synthesis of 3-methylthiofurans from homopropargylic alcohols and DMSO via a tandem sulfenylation/cyclization reaction in a one-pot manner
Organic Chemistry Frontiers, 2016, 3, 1746
1553533 CIFC24 H21 N OP 1 21/c 19.2943; 18.714; 20.557
90; 95.79; 90
3557.3Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553534 CIFC24 H19 NP b c a11.335; 7.4991; 37.869
90; 90; 90
3219Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553535 CIFC42 H34 Cl7 N3 PdP -110.641; 10.978; 17.744
100.04; 106.43; 93.41
1944.7Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553536 CIFC44 H40 Cl N3 PdR -3 :H36.49; 36.49; 21.305
90; 90; 120
24567Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553537 CIFC33 H25 Cl3 N2 O PdP 1 21/c 111.611; 19.188; 13.466
90; 113.15; 90
2758.5Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553538 CIFC34 H27 Cl N2 O PdP 1 21/n 114.187; 12.38; 14.674
90; 92.59; 90
2574.6Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553539 CIFC40 H33 N3 O0P 1 21/c 111.91; 32.793; 9.4655
90; 113.37; 90
3393.6Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553540 CIFC50 H50 N2 O6 S2P 1 21/c 112.0255; 18.091; 10.1121
90; 105.935; 90
2115.4Michelet, Bastien; Tang, Shun; Thiery, Guillaume; Monot, Julien; Li, Huijing; Guillot, Régis; Bour, Christophe; Gandon, Vincent
Catalytic applications of [IPr·GaX2][SbF6] and related species
Organic Chemistry Frontiers, 2016, 3, 1603
1553541 CIFC18 H22 O4P b c a7.6825; 17.5861; 22.9639
90; 90; 90
3102.5Michelet, Bastien; Tang, Shun; Thiery, Guillaume; Monot, Julien; Li, Huijing; Guillot, Régis; Bour, Christophe; Gandon, Vincent
Catalytic applications of [IPr·GaX2][SbF6] and related species
Organic Chemistry Frontiers, 2016, 3, 1603
1553542 CIFC20 H13 F SP 1 21/c 16.0149; 13.4117; 18.2153
90; 91.601; 90
1468.86Wang, Xiaoming; Gensch, Tobias; Glorius, Frank
Highly selective synthesis of 6-substituted benzothiophenes by Sc(OTf)3-catalyzed intermolecular cyclization and sulfur migration
Organic Chemistry Frontiers, 2016, 3, 1619
1553543 CIFC22 H21 N O2P 1 21/n 17.348; 22.781; 11.236
90; 101.092; 90
1845.7Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong
Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides
Organic Chemistry Frontiers, 2017, 4, 77
1553544 CIFC15 H16 N2 O3P 1 21/n 19.3103; 4.8793; 30.741
90; 96.596; 90
1387.3Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong
Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides
Organic Chemistry Frontiers, 2017, 4, 77
1553545 CIFC25 H21 N O2 SR 3 c :H33.922; 33.922; 11.008
90; 90; 120
10970Gong, Xinxing; Li, Guangming; Wu, Jie
Synthesis of polycyclic sultams via a palladium-catalyzed reaction of 1-bromo-2-(cyclopropylidenemethyl)benzenes with 2-alkynylbenzenesulfonamides
Organic Chemistry Frontiers, 2017, 4, 14
1553546 CIFC24 H28 O8P 1 21/c 116.1503; 8.3426; 18.1574
90; 108.184; 90
2324.3Cao, Tao; Ma, Shengming
Nickel-catalyzed alkyl-zincation and carboxylation of diynes
Organic Chemistry Frontiers, 2016, 3, 1711
1553547 CIFC18 H12 Br2P 1 21/n 15.3248; 17.2473; 7.6729
90; 96.167; 90
700.59Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553548 CIFC20 H16 Br2P 1 21/c 16.6723; 8.653; 15.099
90; 111.66; 90
810.2Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553549 CIFC28 H16 Br2C 1 2/c 121.802; 4.9336; 18.875
90; 90.188; 90
2030.2Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553550 CIFC36 H32 Br2P -110.0648; 11.6684; 12.2462
77.981; 86.017; 79.287
1381.44Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553551 CIFC34 H28 Br2P 1 21/n 111.131; 10.249; 11.763
90; 101.301; 90
1315.92Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553552 CIFC50 H38P -110.8252; 13.5794; 14.2122
114.377; 91.316; 95.604
1889.2Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553553 CIFC19 H17 Cl OP 1 21 15.828; 8.2327; 16.8844
90; 98.492; 90
801.23Luo, Hongwen; Yu, Yihua; Ma, Shengming
Suzuki coupling for preparation of allenes – ligand effects and chirality transfer
Organic Chemistry Frontiers, 2016, 3, 1705
1553554 CIFC18 H15 I O SeC 1 2/c 120.3; 5.882; 27.651
90; 94.075; 90
3293Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson
Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives
Organic Chemistry Frontiers, 2017, 4, 277
1553555 CIFC20 H19 I O SeP 1 2/c 119.0809; 5.7136; 17.2112
90; 100.175; 90
1846.87Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson
Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives
Organic Chemistry Frontiers, 2017, 4, 277
1553556 CIFC29 H25 Cl N2 O8 SP 1 21 111.4186; 9.7011; 13.152
90; 92.473; 90
1455.5He, Fu-Sheng; Li, Cong-Shan; Deng, Hua; Zheng, Xing; Yang, Zhong-Tao; Deng, Wei-Ping
The facile and stereoselective synthesis of pyrrolidine β-amino acids via copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition
Organic Chemistry Frontiers, 2017, 4, 52
1553557 CIFC25 H18 O2P n 21 a14.3717; 5.917; 21.4597
90; 90; 90
1824.88Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G.
Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans
Organic Chemistry Frontiers, 2017, 4, 972
1553558 CIFC20 H14 OP 21 21 217.9447; 10.3826; 17.0108
90; 90; 90
1403.16Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G.
Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans
Organic Chemistry Frontiers, 2017, 4, 972
1553559 CIFC27 H31 N O7 S3P 1 21/c 121.226; 8.2493; 16.985
90; 109.61; 90
2801.6Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei
tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes
Organic Chemistry Frontiers, 2017, 4, 135
1553560 CIFC15 H21 N O3 SC 1 2/c 125.961; 5.793; 22.2512
90; 114.088; 90
3055Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei
tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes
Organic Chemistry Frontiers, 2017, 4, 135
1553561 CIFC18 H16 F3 N O2 S2P -16.52; 8.149; 18.175
102.278; 95.21; 97.731
927.9Chen, Min-Tao; Tang, Xiang-Ying; Shi, Min
A facile approach for the trifluoromethylthiolation of methylenecyclopropanes
Organic Chemistry Frontiers, 2017, 4, 86
1553562 CIFC17 H15 N O2P -113.451; 14.313; 15.248
86.714; 63.827; 90.014
2629.2Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai
Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles
Organic Chemistry Frontiers, 2017, 4, 124
1553563 CIFC26 H20 Cl N O3P -17.3875; 11.6702; 13.4944
64.647; 82.911; 77.69
1026.5Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai
Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles
Organic Chemistry Frontiers, 2017, 4, 124
1553564 CIFC23 H24 N2 O6 SP -18.5455; 12.047; 12.1501
60.733; 81.883; 87.112
1079.97Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai
Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles
Organic Chemistry Frontiers, 2017, 4, 124
1553565 CIFC44 H52 N4 S4P -19.3265; 9.7095; 23.593
78.225; 84.998; 75.52
2023.6Xia, Debin; Keerthi, Ashok; An, Cunbin; Baumgarten, Martin
Synthesis of a quinoidal dithieno[2,3-d;2′,3′-d]benzo[2,1-b;3,4-b′]-dithiophene based open-shell singlet biradicaloid
Organic Chemistry Frontiers, 2017, 4, 18
1553566 CIFC20 H21 N O8P 1 21/c 18.101; 19.041; 13.693
90; 107.19; 90
2017.8Zhang, Li; Zhang, Beichen; Jiang, Teng; Lu, Tao; Zhou, Qingfa
Synthesis of tricyclic 3-hydroxyisoindolin-1-ones via triethylamine-catalyzed domino reactions of electron-deficient alkynes with phthalimidomalonate derivatives
Organic Chemistry Frontiers, 2017, 4, 119
1553567 CIFC22 H16 Cl N O2P 1 21/n 111.366; 11.305; 14.788
90; 110.536; 90
1779.4Zhu, Chao-Qun; Deng, Zhuo-Fei; Zhang, Yahong; Wang, You-Qing
Synthesis of 4-substituted 3-(2-hydroxyphenyl)-quinolines through an unexpected iron(iii) chloride promoted reaction of cyclic imine dibenzo[b,f][1,4]oxazepines with alkynes
Organic Chemistry Frontiers, 2017, 4, 196
1553568 CIFC33 H30 N4 O3P 1 21 18.902; 13.209; 12.059
90; 99.65; 90
1397.9Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang
Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst
Organic Chemistry Frontiers, 2017, 4, 101
1553569 CIFC31 H27 Br N4 O3P 21 21 219.662; 12.286; 24.441
90; 90; 90
2901Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang
Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst
Organic Chemistry Frontiers, 2017, 4, 101
1553570 CIFC25 H23 N O3P 418.4091; 8.4091; 29.3175
90; 90; 90
2073.13Xu, Meng-Meng; Wang, Hai-Qing; Wan, Ying; He, Guofeng; Yan, Jingjing; Zhang, Shu; Wang, Shu-Liang; Shi, Feng
Catalytic asymmetric substitution of ortho-hydroxybenzyl alcohols with tetronic acid-derived enamines: enantioselective synthesis of tetronic acid-derived diarylmethanes
Organic Chemistry Frontiers, 2017, 4, 358
1553571 CIFC15 H17 Cl N2 O3P 21 21 217.2915; 12.7983; 15.9552
90; 90; 90
1488.92Peng, Xiao-Jiao; Ho, Yee Ann; Wang, Zhi-Peng; Shao, Pan-Lin; Zhao, Yu; He, Yun
Formal [3 + 2] cycloaddition of α-unsubstituted isocyanoacetates and methyleneindolinones: enantioselective synthesis of spirooxindoles
Organic Chemistry Frontiers, 2017, 4, 81
1553572 CIFC15 H11 Cl F3 N3 O3P 21 21 217.74798; 9.1129; 21.719
90; 90; 90
1533.5Hao, Xin-Qi; Wang, Cong; Liu, Shuang-Liang; Wang, Xiao; Wang, Li; Gong, Jun-Fang; Song, Mao-Ping
Cobalt(ii)/(imidazoline–oxazoline)-catalyzed enantioselective Michael addition of 2-acetyl azaarenes to β-CF3-β-disubstituted nitroalkenes
Organic Chemistry Frontiers, 2017, 4, 308
1553573 CIFC14 H13 N3 O SP -17.68; 8.494; 11.449
85.96; 77.314; 66.467
667.9Chen, Jichao; Wang, Tianyu; Wang, Tong; Lin, Aijun; Yao, Hequan; Xu, Jinyi
Copper-catalyzed C5-selective thio/selenocyanation of 8-aminoquinolines
Organic Chemistry Frontiers, 2017, 4, 130
1553574 CIFC19 H23 Br N O3 PP 21 21 29.8916; 26.4389; 7.7778
90; 90; 90
2034.1Wang, Xubin; Wang, Xiaoming; Han, Zhaobin; Wang, Zheng; Ding, Kuiling
Palladium-catalyzed asymmetric allylic amination: enantioselective synthesis of chiral α-methylene substituted β-aminophosphonates
Organic Chemistry Frontiers, 2017, 4, 271
1553575 CIFC153.47 H187.47 Cl4.41 N2 Si8P 41 21 221.2715; 21.2715; 64.3247
90; 90; 90
29105.4Ushiyama, Ayako; Hiroto, Satoru; Yuasa, Junpei; Kawai, Tsuyoshi; Shinokubo, Hiroshi
Synthesis of a figure-eight azahelicene dimer with high emission and CPL properties
Organic Chemistry Frontiers, 2017, 4, 664
1553576 CIFC21 H21 Cl F N O2P 1 21/c 19.4639; 21.8249; 9.3192
90; 104.752; 90
1861.42Li, Jianxiao; Hu, Weigao; Li, Chunsheng; Yang, Shaorong; Wu, Wanqing; Jiang, Huanfeng
Palladium-catalyzed cascade reaction of haloalkynes with unactivated alkenes for assembly of functionalized oxetanes
Organic Chemistry Frontiers, 2017, 4, 373
1553577 CIFC15 H15 Br O2P 1 21 17.813; 5.321; 15.394
90; 91.594; 90
639.7Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian
Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities
Organic Chemistry Frontiers, 2017, 4, 1084
1553578 CIFC11 H14 Br F O2P 21 21 215.651; 16.364; 38.4918
90; 90; 90
3559Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian
Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities
Organic Chemistry Frontiers, 2017, 4, 1084
1553579 CIFC17 H12 B F2 N5 OC 1 2/c 110.248; 14.634; 11.146
90; 107.352; 90
1595.5Barbon, Stephanie M.; Novoa, Samantha; Bender, Desiree; Groom, Hilary; Luyt, Leonard G.; Gilroy, Joe B.
Copper-assisted azide‒alkyne cycloaddition chemistry as a tool for the production of emissive boron difluoride 3-cyanoformazanates
Organic Chemistry Frontiers, 2017, 4, 178
1553580 CIFC16 H10 Br2 Cl F3P -17.3184; 13.4865; 17.4149
101.672; 94.139; 101.918
1635.33Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553581 CIFC20 H20 Br F3 OP -17.8481; 10.5581; 12.2042
75.472; 72.741; 72.301
905.55Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553582 CIFC20 H20 Br F3 O2P -18.3533; 9.4941; 12.1934
100.216; 97.306; 100.289
923.7Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553583 CIFC18 H15 Br2 F3P b c a16.4974; 6.84171; 28.6498
90; 90; 90
3233.72Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553584 CIFC16 H11 Br2 F3P -17.1399; 9.7404; 22.8361
97.673; 97.146; 106.455
1487.32Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553585 CIFC17 H12 Br F3C 1 2/c 122.8229; 7.4881; 16.5828
90; 102.102; 90
2771Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553586 CIFC19 H17 Br Cl F3P 1 21/c 18.2233; 22.8182; 10.0565
90; 109.447; 90
1779.36Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553587 CIFC12 H11 I N2 O2C m c e6.9379; 19.798; 17.773
90; 90; 90
2441.2He, Xin; Xu, Yi-zhu; Kong, Ling-xuan; Wu, Huan-huan; Ji, De-zhong; Wang, Zhi-bin; Xu, Yun-gen; Zhu, Qi-hua
Copper(i) and N-fluorobenzenesulfonimide-mediated direct regioselective halogenation of 8-amidoquinolines on the C5 position
Organic Chemistry Frontiers, 2017, 4, 1046
1553588 CIFC46 H66 Cl2P 1 21/n 110.4263; 10.2668; 40.789
90; 90.6212; 90
4366Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.
Polymerization of acetylene: polyynes, but not carbyne
Organic Chemistry Frontiers, 2017, 4, 668
1553589 CIFC47 H64P -110.3367; 10.4631; 19.275
88.5549; 78.0127; 88.5903
2038.2Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.
Polymerization of acetylene: polyynes, but not carbyne
Organic Chemistry Frontiers, 2017, 4, 668
1553590 CIFC49 H64P 3 1 c14.154; 14.154; 12.123
90; 90; 120
2103.3Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.
Polymerization of acetylene: polyynes, but not carbyne
Organic Chemistry Frontiers, 2017, 4, 668
1553591 CIFC20 H13 F7 N2 OP 1 21/c 17.858; 26.656; 8.984
90; 90.001; 90
1881.8Xu, Jun; Qiao, Li; Ying, Beibei; Zhu, Xiaolei; Shen, Chao; Zhang, Pengfei
Transition-metal-free direct perfluoroalkylation of quinoline amides at C5 position through radical cross-coupling under mild conditions
Organic Chemistry Frontiers, 2017, 4, 1116
1553592 CIFC44 H58 N2 Se2 Si4P 1 21/n 114.2771; 14.228; 22.6224
90; 99.427; 90
4533.33Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.
Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties
Organic Chemistry Frontiers, 2017, 4, 682
1553593 CIFC44 H58 N2 S2 Si4P 1 21/n 114.2494; 14.1245; 22.4876
90; 98.8; 90
4472.7Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.
Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties
Organic Chemistry Frontiers, 2017, 4, 682
1553594 CIFC32 H22 Br8 N2P -110.8503; 12.4427; 12.9897
100.306; 91.28; 108.652
1628.82Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.
Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties
Organic Chemistry Frontiers, 2017, 4, 682
1553595 CIFC50 H52 N14 O4P 1 21/c 19.842; 21.609; 25.234
90; 91.32; 90
5365.2Zhang, Qian; Wang, Mei-Xiang
Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule
Organic Chemistry Frontiers, 2017, 4, 283
1553596 CIFC54.83 H62.12 Cl1.76 N16.83 O2C 1 2/c 128.402; 9.816; 18.722
90; 90.7; 90
5219.2Zhang, Qian; Wang, Mei-Xiang
Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule
Organic Chemistry Frontiers, 2017, 4, 283
1553597 CIFC54 H60 N16 O2P -19.6636; 15.1098; 18.1939
69.768; 84.466; 84.513
2475.53Zhang, Qian; Wang, Mei-Xiang
Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule
Organic Chemistry Frontiers, 2017, 4, 283
1553598 CIFC40 H24 S2P -17.5051; 8.6296; 11.6509
73.729; 77.669; 77.532
697.78Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung
The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices
Organic Chemistry Frontiers, 2017, 4, 675
1553599 CIFC46 H32P n a 2116.8864; 7.4906; 24.7447
90; 90; 90
3129.94Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung
The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices
Organic Chemistry Frontiers, 2017, 4, 675
1553600 CIFC44 H28P -17.597; 8.9994; 11.0344
78.931; 75.805; 83.409
715.94Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung
The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices
Organic Chemistry Frontiers, 2017, 4, 675
1553601 CIFC26 H22 N4 O5 SC 1 2/c 126.478; 8.1615; 23.0582
90; 96.411; 90
4951.7Chen, Dianpeng; Xing, Gangdong; Yao, Jinzhong; Zhou, Hongwei
Applicable β-sulfonium carbanions: facile construction of thiophene derivatives
Organic Chemistry Frontiers, 2017, 4, 1042
1553602 CIFC12 H9 N O S3P b c n7.9629; 16.9905; 18.7808
90; 90; 90
2540.92Chen, Qiao; Lei, Yingjie; Wang, Yanfang; Wang, Chao; Wang, Yanan; Xu, Zhaoqing; Wang, Huan; Wang, Rui
Direct thiocyanation of ketene dithioacetals under transition-metal-free conditions
Organic Chemistry Frontiers, 2017, 4, 369
1553603 CIFC71 H46 B F24 Ir N O PP 21 21 2112.2302; 15.3106; 36.571
90; 90; 90
6848Wang, Qian; Zhang, Zongpeng; Chen, Caiyou; Yang, Hailong; Han, Zhengyu; Dong, Xiu-Qin; Zhang, Xumu
Iridium catalysts with modular axial-unfixed biphenyl phosphine‒oxazoline ligands: asymmetric hydrogenation of α,β-unsaturated carboxylic acids
Organic Chemistry Frontiers, 2017, 4, 627
1553604 CIFC26 H16 Cu N4 O8P 1 21/c 111.1134; 21.1702; 9.8578
90; 101.189; 90
2275.19Baur, Andreas; Bustin, Katelyn A.; Aguilera, Ellen; Petersen, Jeffrey L.; Hoover, Jessica M.
Copper and silver benzoate and aryl complexes and their implications for oxidative decarboxylative coupling reactions
Organic Chemistry Frontiers, 2017, 4, 519
1553605 CIFC16 H11 N O3P 1 21/c 18.269; 9.296; 16.904
90; 93.281; 90
1297.3Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun
Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones
Organic Chemistry Frontiers, 2017, 4, 292
1553606 CIFC22 H15 N O2P b c a8.874; 13.733; 27.215
90; 90; 90
3317Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun
Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones
Organic Chemistry Frontiers, 2017, 4, 292
1553607 CIFC19 H12 N2 O4P -18.066; 8.242; 12.157
92.727; 102.604; 98.233
778Li, Yingying; Gao, Mingchun; Liu, Bingxin; Xu, Bin
Copper nitrate-mediated chemo- and regioselective annulation from two different alkynes: a direct route to isoxazoles
Organic Chemistry Frontiers, 2017, 4, 445
1553608 CIFC26 H31 F2 N O3P -19.4574; 9.9936; 14.0156
89.023; 76.071; 71.074
1213.5Xu, Jian; Song, Qiuling
Synthesis of fully-substituted 1,2,3-triazoles via copper(i)-catalyzed three-component coupling of sulfoximines, alkynes and azides
Organic Chemistry Frontiers, 2017, 4, 938
1553609 CIFC41 H40 O11P -19.7469; 13.1171; 17.5212
70.806; 75.292; 73.524
1996.5Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng
Total synthesis of I3,II8-biapigenin and ridiculuflavone A
Organic Chemistry Frontiers, 2017, 4, 578
1553610 CIFC43 H46 O11P -115.1534; 15.8118; 17.7296
68.774; 76.898; 79.352
3832Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng
Total synthesis of I3,II8-biapigenin and ridiculuflavone A
Organic Chemistry Frontiers, 2017, 4, 578
1553611 CIFC31 H23 Cl0 N O4P 21 21 219.9046; 10.4946; 23.736
90; 90; 90
2467.2Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding
Organocatalytic C‒C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins
Organic Chemistry Frontiers, 2017, 4, 560
1553612 CIFC30 H21 N O3P 1 21/n 19.263; 16.211; 15.413
90; 91.21; 90
2313.9Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding
Organocatalytic C–C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins
Organic Chemistry Frontiers, 2017, 4, 560
1553613 CIFC38.5 H33 Cl O3P -112.3342; 12.422; 20.4886
94.35; 97.642; 100.981
3037.8Zhang, Yuexia; Wu, Xingxing; Hao, Lin; Wong, Zeng Rong; Lauw, Sherman J. L.; Yang, Song; Webster, Richard D.; Chi, Yonggui Robin
Trimerization of enones under air enabled by NHC/NaOtBu via a SET radical pathway
Organic Chemistry Frontiers, 2017, 4, 467
1553614 CIFC13 H12 N2 OP n a 219.077; 10.4; 11.75
90; 90; 90
1109.2Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming
A copper-catalyzed arylation/nucleophilic addition/fragmentation/C–S bond formation cascade: synthesis of bis(arylthio)imines
Organic Chemistry Frontiers, 2017, 4, 510
1553615 CIFC23 H19 N O2 S2P 21 21 218.189; 14.782; 17.421
90; 90; 90
2108.8Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming
A copper-catalyzed arylation/nucleophilic addition/fragmentation/C–S bond formation cascade: synthesis of bis(arylthio)imines
Organic Chemistry Frontiers, 2017, 4, 510
1553616 CIFC22 H24 S4 Si2P 1 21/c 110.5479; 16.6; 13.9079
90; 92.242; 90
2433.3Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua
Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi
Organic Chemistry Frontiers, 2017, 4, 1019
1553617 CIFC44 H72 Li4 O4 S4 Si4I 41/a :220.763; 20.763; 13.7545
90; 90; 90
5929.6Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua
Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi
Organic Chemistry Frontiers, 2017, 4, 1019
1553618 CIFC17 H17 N O4P -15.7832; 10.4921; 12.3215
90.576; 97.913; 93.157
739.28Chen, Hui; Lin, Cong; Xiong, Chunhua; Liu, Zhanxiang; Zhang, Yuhong
One-pot synthesis of fluorescent 2,4-dialkenylindoles by rhodium-catalyzed dual C–H functionalization
Organic Chemistry Frontiers, 2017, 4, 455
1553619 CIFC21 H17 F OP 1 21/c 113.585; 12.569; 9.741
90; 106.741; 90
1592.8Cao, Tongxiang; Chen, Kai; Zhu, Shifa
An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes
Organic Chemistry Frontiers, 2017, 4, 450
1553620 CIFC23 H26 OP 1 21/c 112.3103; 20.299; 6.9248
90; 95.884; 90
1721.3Cao, Tongxiang; Chen, Kai; Zhu, Shifa
An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes
Organic Chemistry Frontiers, 2017, 4, 450
1553621 CIFC60 H28 F20 N6 O2P -112.4994; 13.1859; 16.0253
102.651; 95.439; 92.29
2560.5Almeida, José; Aguiar, António; Leite, Andreia; Silva, André M. N.; Cunha-Silva, Luís; de Castro, Baltazar; Rangel, Maria; Barone, Giampaolo; Tomé, Augusto C.; Silva, Ana M. G.
1,3-Dipolar cycloadditions with meso-tetraarylchlorins ‒ site selectivity and mixed bisadducts
Organic Chemistry Frontiers, 2017, 4, 534
1553622 CIFC23 H30 N4 O2 SiP b c a15.6516; 14.7041; 20.8303
90; 90; 90
4793.9Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.
Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry
Organic Chemistry Frontiers, 2017, 4, 978
1553623 CIFC20 H21 N5 O2 SiP -19.4684; 10.4692; 12.771
96.2634; 95.7478; 113.644
1138.27Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.
Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry
Organic Chemistry Frontiers, 2017, 4, 978
1553624 CIFC14 H8 Br3 N3P 1 21/n 116.2913; 10.0932; 19.7897
90; 112.895; 90
2997.7Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.
Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry
Organic Chemistry Frontiers, 2017, 4, 978
1553625 CIFC21 H34 N4 O2 SiP b c a8.9462; 11.9145; 43.549
90; 90; 90
4641.9Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.
Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry
Organic Chemistry Frontiers, 2017, 4, 978
1553626 CIFC25 H20 O4P 1 21/c 111.9761; 15.4866; 11.0055
90; 106.167; 90
1960.46Mao, Wenbin; Zhu, Chen
Efficient synthesis of multiply substituted butenolides from keto acids and terminal alkynes promoted by combined acids
Organic Chemistry Frontiers, 2017, 4, 1029
1553627 CIFC35 H18 Fe O4P -18.8576; 9.515; 15.8743
79.571; 74.479; 86.413
1267.66Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553628 CIFC32 H18 OP 1 21/n 112.737; 10.827; 15.738
90; 105.708; 90
2089.3Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553629 CIFC51 H29 Cl3 O4P 21 21 2110.5417; 14.8356; 24.1274
90; 90; 90
3773.3Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553630 CIFC51 H30 Cl2 OP 1 21/n 112.3541; 20.5251; 15.593
90; 111.562; 90
3677.21Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553631 CIFC51 H30 Cl2P 1 21/n 112.2233; 20.4397; 15.612
90; 111.759; 90
3622.59Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553632 CIFC20 H19 Br N2 O5 SP 21 21 218.8208; 12.857; 18.1141
90; 90; 90
2054.3Yu, Lu; Cheng, Yuyu; Qi, Fei; Li, Rou; Li, Pengfei
Organocatalytic regioselective, diastereoselective, and enantioselective annulation of cyclic 1-azadienes with γ-nitro ketones via 3,4-cyclization
Organic Chemistry Frontiers, 2017, 4, 1336
1553633 CIFC29 H25 N3P -15.768; 9.924; 20.463
100.063; 91.086; 92.46
1151.8Zhao, Fen; Liu, Yaowen; Yang, Shu; Xie, Kai; Jiang, Yubo
Pd-catalyzed selective N(3)-ortho C–H arylation of 1,4-disubstituted 1,2,3-triazoles
Organic Chemistry Frontiers, 2017, 4, 1112
1553634 CIFC21 H15 Br2 N O2P 1 21/n 116.003; 7.036; 16.456
90; 101.876; 90
1813.2Qiu, Guanyinsheng; Li, Yuewen; Ma, Lele; Zhou, Hongwei
KBr/K2S2O8-mediated dibromohydration of N-(2-alkynylaryl)acetamide
Organic Chemistry Frontiers, 2017, 4, 1069
1553635 CIFC33 H31 N O3P 1 21/n 115.552; 9.109; 20
90; 111.508; 90
2636Liu, Feng; Tian, Jiaxin; Liu, Yong; Tao, Chuangan; Zhu, Hao; Zhang, Aina; Xu, Dongfang; Zhao, Baoguo
Decarboxylative Umpolung of conjugated enals to β-carbanions for intramolecular nucleophilic addition to an aldehyde
Organic Chemistry Frontiers, 2017, 4, 1586
1553636 CIFC25 H20 N2 O2 SP 21 21 217.7445; 13.971; 19.15
90; 90; 90
2072Lin, Ye; Liu, Lei; Du, Da-Ming
Squaramide-catalyzed asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles with chalcones for synthesis of pyrrolidinyl spirooxindoles
Organic Chemistry Frontiers, 2017, 4, 1229
1553637 CIFC16 H21 N3 O5P 21 21 218.4855; 15.887; 25.5299
90; 90; 90
3441.7Deng, Tao; Thota, Ganesh Kumar; Li, Yi; Kang, Qiang
Enantioselective conjugate addition of hydroxylamines to α,β-unsaturated 2-acyl imidazoles catalyzed by a chiral-at-metal Rh(iii) complex
Organic Chemistry Frontiers, 2017, 4, 573
1553638 CIFC36 H40 N2 O4P 1 21/c 111.882; 6.1567; 22.083
90; 99.617; 90
1592.8Purc, Anna; Koszarna, Beata; Iachina, Irina; Friese, Daniel H.; Tasior, Mariusz; Sobczyk, Krzysztof; Pędziński, Tomasz; Brewer, Jonathan; Gryko, Daniel T.
The impact of interplay between electronic and steric effects on the synthesis and the linear and non-linear optical properties of diketopyrrolopyrrole bearing benzofuran moieties
Organic Chemistry Frontiers, 2017, 4, 724
1553639 CIFC32 H38 N2 O2 S3P 1 21/c 120.477; 5.2589; 28.0402
90; 101.007; 90
2964Chen, Wangqiao; Nakano, Masahiro; Takimiya, Kazuo; Zhang, Qichun
Selective thionation of naphtho[2,3-b]thiophene diimide: tuning of the optoelectronic properties and packing structure
Organic Chemistry Frontiers, 2017, 4, 704
1553640 CIFC19 H18 N2 O3P 43 21 29.37666; 9.37666; 36.6305
90; 90; 90
3220.62Zhang, Yun; Xue, Yibin; Li, Gang; Yuan, Haosen; Luo, Tuoping
Enantioselective synthesis of <i>Iboga</i> alkaloids and vinblastine <i>via</i> rearrangements of quaternary ammoniums.
Chemical science, 2016, 7, 5530-5536
1553641 CIFC19.5 H24.5 Cl1.5 N2P 1 21/c 113.023; 21.0779; 12.8028
90; 90.541; 90
3514.2Zhang, Yun; Xue, Yibin; Li, Gang; Yuan, Haosen; Luo, Tuoping
Enantioselective synthesis of <i>Iboga</i> alkaloids and vinblastine <i>via</i> rearrangements of quaternary ammoniums.
Chemical science, 2016, 7, 5530-5536
1553642 CIFC18 H19 N3A e a 212.2491; 35.949; 13.088
90; 90; 90
5763.2Zhang, Yun; Xue, Yibin; Li, Gang; Yuan, Haosen; Luo, Tuoping
Enantioselective synthesis of <i>Iboga</i> alkaloids and vinblastine <i>via</i> rearrangements of quaternary ammoniums.
Chemical science, 2016, 7, 5530-5536
1553643 CIFC27 H33 B2 F11 Fe N6F -4 3 c29.3374; 29.3374; 29.3374
90; 90; 90
25250.2Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David
Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers.
Chemical science, 2017, 8, 2448-2456
1553644 CIFC26 H31.5 B2 F10 Fe N6.5P -111.4603; 14.9231; 18.6992
110.254; 106.434; 91.133
2853Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David
Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers.
Chemical science, 2017, 8, 2448-2456
1553645 CIFC25 H30 B2 F10 N6 ZnP 1 c 113.6092; 14.5112; 14.1222
90; 90.875; 90
2788.61Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David
Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers.
Chemical science, 2017, 8, 2448-2456
1553646 CIFC24 H27 B2 F11 Fe N6P 316.8376; 16.8376; 7.8829
90; 90; 120
1935.43Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David
Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers.
Chemical science, 2017, 8, 2448-2456
1553647 CIFC27 H33 B2 F11 N6 ZnF -4 3 c29.282; 29.282; 29.282
90; 90; 90
25107.4Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David
Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers.
Chemical science, 2017, 8, 2448-2456
1553648 CIFC8 H8 F6 N4 Ni Si Xe0.34P 4/m m m7.0187; 7.0187; 7.5098
90; 90; 90
369.95Elsaidi, Sameh K.; Mohamed, Mona H.; Simon, Cory M.; Braun, Efrem; Pham, Tony; Forrest, Katherine A.; Xu, Wenqian; Banerjee, Debasis; Space, Brian; Zaworotko, Michael J.; Thallapally, Praveen K.
Effect of ring rotation upon gas adsorption in SIFSIX-3-M (M = Fe, Ni) pillared square grid networks.
Chemical science, 2017, 8, 2373-2380
1553649 CIFC8 H8 F6 N4 Ni SiP 4/m m m7.00122; 7.00122; 7.49794
90; 90; 90
367.527Elsaidi, Sameh K.; Mohamed, Mona H.; Simon, Cory M.; Braun, Efrem; Pham, Tony; Forrest, Katherine A.; Xu, Wenqian; Banerjee, Debasis; Space, Brian; Zaworotko, Michael J.; Thallapally, Praveen K.
Effect of ring rotation upon gas adsorption in SIFSIX-3-M (M = Fe, Ni) pillared square grid networks.
Chemical science, 2017, 8, 2373-2380
1553650 CIFC8 H8 F6 N4 Ni SiP 4/m m m6.99732; 6.99732; 7.49177
90; 90; 90
366.816Elsaidi, Sameh K.; Mohamed, Mona H.; Simon, Cory M.; Braun, Efrem; Pham, Tony; Forrest, Katherine A.; Xu, Wenqian; Banerjee, Debasis; Space, Brian; Zaworotko, Michael J.; Thallapally, Praveen K.
Effect of ring rotation upon gas adsorption in SIFSIX-3-M (M = Fe, Ni) pillared square grid networks.
Chemical science, 2017, 8, 2373-2380
1553651 CIFC8 H8 F6 Fe N4 O SiP 4/m m m7.1831; 7.1831; 7.5839
90; 90; 90
391.31Elsaidi, Sameh K.; Mohamed, Mona H.; Simon, Cory M.; Braun, Efrem; Pham, Tony; Forrest, Katherine A.; Xu, Wenqian; Banerjee, Debasis; Space, Brian; Zaworotko, Michael J.; Thallapally, Praveen K.
Effect of ring rotation upon gas adsorption in SIFSIX-3-M (M = Fe, Ni) pillared square grid networks.
Chemical science, 2017, 8, 2373-2380
1553652 CIFC6 H8 Bi I4 NP 1 21/c 17.7618; 14.0412; 13.1959
90; 92.959; 90
1436.24Li, Tianyue; Hu, Yue; Morrison, Carole A.; Wu, Wenjun; Han, Hongwei; Robertson, Neil
Lead-free pseudo-three-dimensional organic‒inorganic iodobismuthates for photovoltaic applications
Sustainable Energy & Fuels, 2017, 1, 308
1553653 CIFC5 H6 Bi I4 NP 1 21/c 112.6997; 28.3198; 7.716
90; 95.288; 90
2763.27Li, Tianyue; Hu, Yue; Morrison, Carole A.; Wu, Wenjun; Han, Hongwei; Robertson, Neil
Lead-free pseudo-three-dimensional organic‒inorganic iodobismuthates for photovoltaic applications
Sustainable Energy & Fuels, 2017, 1, 308
1553654 CIFC42 H42 I2 N2P 61 2 215.6598; 15.6598; 34.08
90; 90; 120
7237.7Samanta, Soham; Halder, Senjuti; Dey, Poulomi; Manna, Utsab; Ramesh, Aiyagari; Das, Gopal
A ratiometric fluorogenic probe for the real-time detection of SO<sub>3</sub><sup>2-</sup> in aqueous medium: application in a cellulose paper based device and potential to sense SO<sub>3</sub><sup>2-</sup> in mitochondria.
The Analyst, 2017, 143, 250-257
1553655 CIFC72 H84 N12R -3 :H24.741; 24.741; 19.826
90; 90; 120
10510Slater, A. G.; Little, M. A.; Briggs, M. E.; Jelfs, K. E.; Cooper, A. I.
A solution-processable dissymmetric porous organic cage
Molecular Systems Design & Engineering, 2018, 3, 223
1553656 CIFC73.1 H89.96 Cl1.55 N12 O1.89R -3 :H24.483; 24.483; 19.6123
90; 90; 120
10181Slater, A. G.; Little, M. A.; Briggs, M. E.; Jelfs, K. E.; Cooper, A. I.
A solution-processable dissymmetric porous organic cage
Molecular Systems Design & Engineering, 2018, 3, 223
1553657 CIFC4 H18 N2 O22 Se6 V3P -110.0027; 10.4765; 12.2924
74.478; 72.643; 79.707
1177.8Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553658 CIFC4 H12 N2 O10 Se2 V2P 1 21/c 110.0879; 6.2047; 10.6765
90; 116.566; 90
597.71Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553659 CIFC8 H44 N4 O48 Se12 V6C 1 2/c 118.816; 7.934; 34.439
90; 95.85; 90
5114Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553660 CIFC8 H58.67 N6 O65.33 Se16 V8P 1 21/c 117.999; 15.658; 26.0344
90; 113.803; 90
6713.1Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553661 CIFC8 H43 N4 O47 Se12 V6P 1 21/c 124.713; 7.9212; 34.399
90; 130.376; 90
5129.9Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553662 CIFC46 H38 N6 O4 S2P 1 21/c 116.2355; 14.4863; 17.7924
90; 106.064; 90
4021.2Zhao, Xueqian; Ge, Congwu; Yang, Xiaodi; Gao, Xike
Dithieno[3,2-a:3′,2′-j][5,6,11,12]chrysene diimides and their molecular energy level regulation
Materials Chemistry Frontiers, 2017, 1, 1635
1553663 CIFC26 H18 S2P 1 21/c 15.641; 9.315; 19.216
90; 103.97; 90
979.9Zhang, Jibo; Ma, Suqian; Fang, Honghua; Xu, Bin; Sun, Hongbo; Chan, Im; Tian, Wenjing
Insights into the origin of aggregation enhanced emission of 9,10-distyrylanthracene derivatives
Materials Chemistry Frontiers, 2017, 1, 1422
1553664 CIFC19 H15 B F2 N2P -16.418; 8.632; 14.198
74.951; 81.658; 86.211
751.2Yamaguchi, Madoka; Ito, Shunichiro; Hirose, Amane; Tanaka, Kazuo; Chujo, Yoshiki
Control of aggregation-induced emission versus fluorescence aggregation-caused quenching by bond existence at a single site in boron pyridinoiminate complexes
Materials Chemistry Frontiers, 2017, 1, 1573
1553665 CIFC19 H13 B F2 N2P 1 21/n 19.2376; 11.5433; 13.4497
90; 98.264; 90
1419.3Yamaguchi, Madoka; Ito, Shunichiro; Hirose, Amane; Tanaka, Kazuo; Chujo, Yoshiki
Control of aggregation-induced emission versus fluorescence aggregation-caused quenching by bond existence at a single site in boron pyridinoiminate complexes
Materials Chemistry Frontiers, 2017, 1, 1573
1553666 CIFC20 H14 Hg I2 N2 S2P -110.2226; 10.3008; 12.2126
74.477; 67.707; 71.185
1110.69Gabr, Moustafa T.; Christopher Pigge, F.
A turn-on AIE active fluorescent sensor for Hg2+ by combination of 1,1-bis(2-pyridyl)ethylene and thiophene/bithiophene fragments
Materials Chemistry Frontiers, 2017, 1, 1654
1553667 CIFC18 H16 Cl4 N4 O2R 3 :H14.7047; 14.7047; 23.9058
90; 90; 120
4476.6Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng
Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties
Materials Chemistry Frontiers, 2017, 1, 1041
1553668 CIFC27 H30 N4 O3P 1 21/c 19.8325; 11.2257; 22.882
90; 98.783; 90
2496Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng
Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties
Materials Chemistry Frontiers, 2017, 1, 1041
1553669 CIFC18 H18 F2 N2.67 O2R -3 :H14.4761; 14.4761; 40.5191
90; 90; 120
7353.5Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng
Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties
Materials Chemistry Frontiers, 2017, 1, 1041
1553670 CIFC30 H34 N4 O6P 21 21 216.29545; 15.9502; 28.8235
90; 90; 90
2894.27Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng
Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties
Materials Chemistry Frontiers, 2017, 1, 1041
1553671 CIFC39 H54 N4 O3P -112.9272; 13.0256; 23.4928
82.005; 79.707; 86.311
3851.2Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng
Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties
Materials Chemistry Frontiers, 2017, 1, 1041
1553672 CIFC21 H23 N O2P 1 21/c 115.43; 10.791; 10.129
90; 101.94; 90
1650Wang, Fang; DeRosa, Christopher A.; Daly, Margaret L.; Song, Daniel; Fraser, Cassandra L.
Multi-stimuli responsive luminescent azepane-substituted β-diketones and difluoroboron complexes.
Materials chemistry frontiers, 2017, 1, 1866-1874
1553673 CIFC42 H29 N O2P -19.4456; 9.9577; 16.2906
102.183; 93.914; 93.086
1490.57Peng, Zhixing; Huang, Kai; Tao, Yuhan; Li, Xihui; Zhang, Lianpeng; Lu, Ping; Wang, Yanguang
Turning on the solid emission from non-emissive 2-aryl-3-cyanobenzofurans by tethering tetraphenylethene for green electroluminescence
Materials Chemistry Frontiers, 2017, 1, 1858
1553674 CIFC42 H29 N O2P -19.4088; 11.452; 15.1598
90.309; 105.929; 93.468
1567.45Peng, Zhixing; Huang, Kai; Tao, Yuhan; Li, Xihui; Zhang, Lianpeng; Lu, Ping; Wang, Yanguang
Turning on the solid emission from non-emissive 2-aryl-3-cyanobenzofurans by tethering tetraphenylethene for green electroluminescence
Materials Chemistry Frontiers, 2017, 1, 1858
1553675 CIFC42 H29 N O2P 1 21/c 118.2932; 19.3313; 9.1613
90; 103.67; 90
3148Peng, Zhixing; Huang, Kai; Tao, Yuhan; Li, Xihui; Zhang, Lianpeng; Lu, Ping; Wang, Yanguang
Turning on the solid emission from non-emissive 2-aryl-3-cyanobenzofurans by tethering tetraphenylethene for green electroluminescence
Materials Chemistry Frontiers, 2017, 1, 1858
1553676 CIFC37 H43 Cu2 I2 N5 O2 S3P -19.102; 14.511; 17.16
66.114; 88.537; 80.515
2041.9Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai
A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules
Materials Chemistry Frontiers, 2017, 1, 1764
1553677 CIFC34 H27 Cu2 I2 N3 O S3P -19.4203; 14.3226; 17.3309
65.977; 77.856; 79.467
2075.6Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai
A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules
Materials Chemistry Frontiers, 2017, 1, 1764
1553678 CIFC30 H34 Cu2 I2 N4 O S3P -19.174; 14.442; 17.023
113.404; 90.013; 99.203
2038Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai
A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules
Materials Chemistry Frontiers, 2017, 1, 1764
1553679 CIFC31 H33 Cu2 I2 N5 S3P -18.962; 14.515; 16.577
112.653; 91.205; 98.338
1962Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai
A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules
Materials Chemistry Frontiers, 2017, 1, 1764
1553680 CIFC31 H39 Cu2 I2 N3 O2 S5P -19.353; 14.189; 17.257
113.336; 94.402; 100.137
2043Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai
A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules
Materials Chemistry Frontiers, 2017, 1, 1764
1553681 CIFC35 H45 Cu2 I2 N5 O2 S3P -19.252; 14.347; 17.158
113.914; 91.45; 99.705
2041.1Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai
A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules
Materials Chemistry Frontiers, 2017, 1, 1764
1553682 CIFC17 H16 I N O2P 21 21 216.1493; 12.443; 19.762
90; 90; 90
1512.1Butler, Tristan; Wang, Fang; Sabat, Michal; Fraser, Cassandra L.
Controlling solid-state optical properties of stimuli responsive dimethylamino-substituted dibenzoylmethane materials
Materials Chemistry Frontiers, 2017, 1, 1804
1553683 CIFC9 H4 N2 O4 Y0.33P 3 1 c12.8501; 12.8501; 15.709
90; 90; 120
2246.4Liu, Kang; Li, Xu; Ma, Dingxuan; Han, Yi; Li, Baiyan; Shi, Zhan; Li, Zhenjiang; Wang, Lei
A microporous yttrium metal‒organic framework of an unusual nia topology for high adsorption selectivity of C2H2and CO2over CH4at room temperature
Materials Chemistry Frontiers, 2017, 1, 1982
1553684 CIFC22 H24 N3 Ni0.5P -18.3884; 8.4668; 14.2802
95.006; 94.479; 113.925
916.34Yoshida, Takuya; Shinokubo, Hiroshi
Direct amination of the antiaromatic NiII norcorrole
Materials Chemistry Frontiers, 2017, 1, 1853
1553685 CIFC37 H24 N2 O3P 1 21/n 124.2035; 9.4392; 24.306
90; 109.203; 90
5244Gan, Shifeng; Zhou, Jian; Smith, Trevor A.; Su, Huifang; Luo, Wenwen; Hong, Yuning; Zhao, Zujin; Tang, Ben Zhong
New AIEgens with delayed fluorescence for fluorescence imaging and fluorescence lifetime imaging of living cells
Materials Chemistry Frontiers, 2017, 1, 2554
1553686 CIFC25 H17 N O2P 1 21/c 18.4792; 29.902; 7.9399
90; 117.656; 90
1783.1Gan, Shifeng; Zhou, Jian; Smith, Trevor A.; Su, Huifang; Luo, Wenwen; Hong, Yuning; Zhao, Zujin; Tang, Ben Zhong
New AIEgens with delayed fluorescence for fluorescence imaging and fluorescence lifetime imaging of living cells
Materials Chemistry Frontiers, 2017, 1, 2554
1553687 CIFC29 H23 N3 O2P 1 21/n 17.3698; 10.7294; 27.0518
90; 90.5158; 90
2138.99Tokuo, Kokichi; Sakai, Hayato; Sakanoue, Tomo; Takenobu, Taishi; Araki, Yasuyuki; Wada, Takehiko; Hasobe, Taku
Control of the electrochemical and photophysical properties of N-substituted benzo[ghi]perylene derivatives
Materials Chemistry Frontiers, 2017, 1, 2299
1553688 CIFC27 H18 Cu2 O11P 63/m m c18.4455; 18.4455; 26.4268
90; 90; 120
7786.7Chen, Fengli; Bai, Dongjie; Wang, Yao; Jiang, Donghao; He, Yabing
A family of ssa-type copper-based MOFs constructed from unsymmetrical diisophthalates: synthesis, characterization and selective gas adsorption
Materials Chemistry Frontiers, 2017, 1, 2283
1553689 CIFC28 H20 Cu2 O11P 63/m m c18.2664; 18.2664; 26.5488
90; 90; 120
7671.5Chen, Fengli; Bai, Dongjie; Wang, Yao; Jiang, Donghao; He, Yabing
A family of ssa-type copper-based MOFs constructed from unsymmetrical diisophthalates: synthesis, characterization and selective gas adsorption
Materials Chemistry Frontiers, 2017, 1, 2283
1553690 CIFC38 H48 Cu2 N4 O16P 63/m m c18.315; 18.315; 26.7665
90; 90; 120
7775.6Chen, Fengli; Bai, Dongjie; Wang, Yao; Jiang, Donghao; He, Yabing
A family of ssa-type copper-based MOFs constructed from unsymmetrical diisophthalates: synthesis, characterization and selective gas adsorption
Materials Chemistry Frontiers, 2017, 1, 2283
1553691 CIFC48 H30 N4P n n a14.768; 15.377; 16.689
90; 90; 90
3790Zhang, Yahui; Kong, Lingwei; Mao, Huiling; Pan, Xiaoling; Shi, Jianbing; Tong, Bin; Dong, Yuping
Light/temperature-enhanced emission characteristics of malononitrile-containing hexaphenyl-1,3-butadiene derivatives: the hotter, the brighter
Materials Chemistry Frontiers, 2017, 1, 2569
1553692 CIFC23.5 H20 B0.5C 1 2/c 110.3419; 16.4056; 20.936
90; 100.537; 90
3492.2Chi, Weijie; Yin, Wenting; Qi, Qingkai; Qiao, Qinglong; Lin, Yuyan; Zhu, Zhuohui; Vijayan, Sindhu; Hashimoto, Michinao; Udayakumar, Gayathri; Xu, Zhaochao; Liu, Xiaogang
Ground-state conformers enable bright single-fluorophore ratiometric thermometers with positive temperature coefficients
Materials Chemistry Frontiers, 2017, 1, 2383
1553693 CIFC29 H34 B Br2 NP -17.9955; 11.139; 14.735
87.095; 78.445; 81.208
1270.3Matsumoto, Takuya; Takamine, Hirofumi; Tanaka, Kazuo; Chujo, Yoshiki
Design of bond-cleavage-induced intramolecular charge transfer emission with dibenzoboroles and their application to ratiometric sensors for discriminating chain lengths of alkanes
Materials Chemistry Frontiers, 2017, 1, 2368
1553694 CIFC38 H27 Br2 N O2C 1 2/c 119.61; 15.469; 20.516
90; 107.135; 90
5947.2Gopikrishna, Peddaboodi; Raman Adil, Laxmi; Iyer, Parameswar Krishnan
Bridge-driven aggregation control in dibenzofulvene–naphthalimide based donor–bridge–acceptor systems: enabling fluorescence enhancement, blue to red emission and solvatochromism
Materials Chemistry Frontiers, 2017, 1, 2590
1553695 CIFC38 H29 N O2P 1 21/c 111.2762; 13.9376; 17.8045
90; 101.143; 90
2745.5Gopikrishna, Peddaboodi; Raman Adil, Laxmi; Iyer, Parameswar Krishnan
Bridge-driven aggregation control in dibenzofulvene–naphthalimide based donor–bridge–acceptor systems: enabling fluorescence enhancement, blue to red emission and solvatochromism
Materials Chemistry Frontiers, 2017, 1, 2590
1553696 CIFC42 H28 Cu2 N10 O8P -4 3 n27.6887; 27.6887; 27.6887
90; 90; 90
21227.9Tan, Jing; Zhou, Beibei; Liang, Congcong; Zinky, Hannah; Zhou, Hao-Long; Zhang, Yue-Biao
Secondary-amine-functionalized isoreticular metal‒organic frameworks for controllable and selective dye capture
Materials Chemistry Frontiers, 2018, 2, 129
1553697 CIFC42 H28 N10 O8 Zn2P -4 3 n28.1049; 28.1049; 28.1049
90; 90; 90
22199.7Tan, Jing; Zhou, Beibei; Liang, Congcong; Zinky, Hannah; Zhou, Hao-Long; Zhang, Yue-Biao
Secondary-amine-functionalized isoreticular metal‒organic frameworks for controllable and selective dye capture
Materials Chemistry Frontiers, 2018, 2, 129
1553698 CIFC22 H16 N2 OP -18.7512; 8.8377; 11.1832
90.101; 91.344; 106.984
826.93Zheng, Chao; Zang, Qiguang; Nie, Han; Huang, Weitao; Zhao, Zujin; Qin, Anjun; Hu, Rongrong; Tang, Ben Zhong
Fluorescence visualization of crystal formation and transformation processes of organic luminogens with crystallization-induced emission characteristics
Materials Chemistry Frontiers, 2018, 2, 180
1553699 CIFC22 H16 N2 OP 1 21/c 110.8856; 5.8214; 26.159
90; 95.577; 90
1649.8Zheng, Chao; Zang, Qiguang; Nie, Han; Huang, Weitao; Zhao, Zujin; Qin, Anjun; Hu, Rongrong; Tang, Ben Zhong
Fluorescence visualization of crystal formation and transformation processes of organic luminogens with crystallization-induced emission characteristics
Materials Chemistry Frontiers, 2018, 2, 180
1553700 CIFC22 H16 N2 OP -19.2692; 9.9355; 10.8222
79.332; 65.483; 69.001
845.8Zheng, Chao; Zang, Qiguang; Nie, Han; Huang, Weitao; Zhao, Zujin; Qin, Anjun; Hu, Rongrong; Tang, Ben Zhong
Fluorescence visualization of crystal formation and transformation processes of organic luminogens with crystallization-induced emission characteristics
Materials Chemistry Frontiers, 2018, 2, 180
1553701 CIFC39 H50 N2 O S4P -17.622; 14.074; 18.644
108.82; 99.259; 95.596
1844.3Hashikawa, Yoshifumi; Yasui, Hidefumi; Kurotobi, Kei; Murata, Yasujiro
Synthesis and properties of open-cage fullerene C60 derivatives: impact of the extended π-conjugation
Materials Chemistry Frontiers, 2018, 2, 206
1553702 CIFC26 H34 B20P -17.1876; 10.559; 10.841
77.421; 88.462; 76.313
779.9Mori, Hiroki; Nishino, Kenta; Wada, Keisuke; Morisaki, Yasuhiro; Tanaka, Kazuo; Chujo, Yoshiki
Modulation of luminescence chromic behaviors and environment-responsive intensity changes by substituents in bis-o-carborane-substituted conjugated molecules
Materials Chemistry Frontiers, 2018, 2, 573
1553703 CIFC28 H34 O4 Si2P 1 21/c 18.3944; 14.3259; 11.7204
90; 90.646; 90
1409.4Shimizu, Masaki; Kinoshita, Takumi; Shigitani, Ryosuke; Miyake, Yusuke; Tajima, Kunihiko
Use of silylmethoxy groups as inducers of efficient room temperature phosphorescence from precious-metal-free organic luminophores
Materials Chemistry Frontiers, 2018, 2, 347
1553704 CIFC48 H42 O4 Si2P 1 21/c 111.7637; 12.6947; 13.4413
90; 92.205; 90
2005.8Shimizu, Masaki; Kinoshita, Takumi; Shigitani, Ryosuke; Miyake, Yusuke; Tajima, Kunihiko
Use of silylmethoxy groups as inducers of efficient room temperature phosphorescence from precious-metal-free organic luminophores
Materials Chemistry Frontiers, 2018, 2, 347
1553705 CIFC34 H46 O4 Si2P -18.0255; 15.7261; 15.9887
111.511; 104.2; 100.188
1738.5Shimizu, Masaki; Kinoshita, Takumi; Shigitani, Ryosuke; Miyake, Yusuke; Tajima, Kunihiko
Use of silylmethoxy groups as inducers of efficient room temperature phosphorescence from precious-metal-free organic luminophores
Materials Chemistry Frontiers, 2018, 2, 347
1553706 CIFC76 H48 Cl20 N4 O18 Ru4P -110.295; 15.211; 15.71
97.505; 103.952; 98.491
2325.7Kosaka, Wataru; Itoh, Masahisa; Miyasaka, Hitoshi
Metamagnetism with TN = 97 K in a layered assembly of paddlewheel [Ru2] units and TCNQ: an empirical rule for interlayer distances determining the magnetic ground state
Materials Chemistry Frontiers, 2018, 2, 497
1553707 CIFC72 H60 O12P -113.2528; 16.273; 18.7976
100.659; 93.188; 98.3918
3927.09Hisaki, Ichiro; Ikenaka, Nobuaki; Tsuzuki, Seiji; Tohnai, Norimitsu
Sterically crowded hydrogen-bonded hexagonal network frameworks
Materials Chemistry Frontiers, 2018, 2, 338
1553708 CIFC72 H60 O12P -114.593; 15.3214; 20.375
102.97; 102.468; 97.238
4261.2Hisaki, Ichiro; Ikenaka, Nobuaki; Tsuzuki, Seiji; Tohnai, Norimitsu
Sterically crowded hydrogen-bonded hexagonal network frameworks
Materials Chemistry Frontiers, 2018, 2, 338
1553709 CIFC60 H24 F12 O12I 1 2/a 112.2591; 38.9347; 18.0305
90; 93.869; 90
8586.4Hisaki, Ichiro; Ikenaka, Nobuaki; Tsuzuki, Seiji; Tohnai, Norimitsu
Sterically crowded hydrogen-bonded hexagonal network frameworks
Materials Chemistry Frontiers, 2018, 2, 338
1553710 CIFC80 H68 O14I 1 2/a 127.8455; 22.4501; 29.8331
90; 95.3352; 90
18568.9Hisaki, Ichiro; Ikenaka, Nobuaki; Tsuzuki, Seiji; Tohnai, Norimitsu
Sterically crowded hydrogen-bonded hexagonal network frameworks
Materials Chemistry Frontiers, 2018, 2, 338
1553711 CIFC63 H55 N6P 1 21/n 114.2255; 29.98; 22.944
90; 92.5721; 90
9775Sakamaki, Daisuke; Saeki, Hidenori; Seki, Shu
Synthesis and properties of a twin donor molecule composed of cofacially stacked dihydrodiazapentacenes
Materials Chemistry Frontiers, 2018, 2, 530
1553712 CIFC63 H58 F6 N6 O SbP 1 21/n 115.927; 13.626; 25.437
90; 106.335; 90
5297.5Sakamaki, Daisuke; Saeki, Hidenori; Seki, Shu
Synthesis and properties of a twin donor molecule composed of cofacially stacked dihydrodiazapentacenes
Materials Chemistry Frontiers, 2018, 2, 530
1553713 CIFC19 H20 I N2 O2P 1 21/c 18.9246; 26.061; 15.999
90; 103.344; 90
3620.6Suzuki, Shuichi; Nakamura, Fumiya; Naota, Takeshi
A direct synthetic method for (nitronyl nitroxide)-substituted π-electronic compounds via a palladium-catalyzed cross-coupling reaction with a zinc complex
Materials Chemistry Frontiers, 2018, 2, 591
1553714 CIFC25 H24 N3 O2 SP -18.9325; 9.7653; 13.1883
81.1923; 77.908; 74.017
1075.8Suzuki, Shuichi; Nakamura, Fumiya; Naota, Takeshi
A direct synthetic method for (nitronyl nitroxide)-substituted π-electronic compounds via a palladium-catalyzed cross-coupling reaction with a zinc complex
Materials Chemistry Frontiers, 2018, 2, 591
1553715 CIFC24 H16 Cl O6 S12C 1 2/c 133.29; 7.227; 13.232
90; 105.227; 90
3072Ueda, Akira; Mori, Hatsumi
A phenol-fused tetrathiafulvalene: modulation of hydrogen-bond patterns and electrical conductivity in the charge-transfer salt
Materials Chemistry Frontiers, 2018, 2, 566
1553716 CIFC12 H8 O S6P 1 21/c 112.369; 11.196; 10.011
90; 92.537; 90
1385Ueda, Akira; Mori, Hatsumi
A phenol-fused tetrathiafulvalene: modulation of hydrogen-bond patterns and electrical conductivity in the charge-transfer salt
Materials Chemistry Frontiers, 2018, 2, 566
1553717 CIFC13 H7P -4 c 214.367; 14.367; 7.992
90; 90; 90
1649.6Xu, Jinjia; Takai, Atsuro; Bannaron, Alisa; Nakagawa, Takafumi; Matsuo, Yutaka; Sugimoto, Manabu; Matsushita, Yoshitaka; Takeuchi, Masayuki
A helically-twisted ladder based on 9,9′-bifluorenylidene: synthesis, characterization, and carrier-transport properties
Materials Chemistry Frontiers, 2018, 2, 780
1553718 CIFC64 H36 Cl4P 1 21/n 118.181; 12.65; 19.801
90; 96.169; 90
4527.7Xu, Jinjia; Takai, Atsuro; Bannaron, Alisa; Nakagawa, Takafumi; Matsuo, Yutaka; Sugimoto, Manabu; Matsushita, Yoshitaka; Takeuchi, Masayuki
A helically-twisted ladder based on 9,9′-bifluorenylidene: synthesis, characterization, and carrier-transport properties
Materials Chemistry Frontiers, 2018, 2, 780
1553719 CIFC61 H62 Cl2 Ge O12 S4P -19.768; 11.2196; 25.3543
88.261; 82.947; 86.248
2751Furukawa, Shunsuke; Hayashi, Keisuke; Yamagishi, Ken; Saito, Masaichi
Synthesis and properties of spiro-type heterasumanenes containing group 14 elements as bridging atoms
Materials Chemistry Frontiers, 2018, 2, 929
1553720 CIFC60 H60 O12 S4 SiP -19.7198; 13.551; 21.616
104.724; 100.877; 95.266
2674.7Furukawa, Shunsuke; Hayashi, Keisuke; Yamagishi, Ken; Saito, Masaichi
Synthesis and properties of spiro-type heterasumanenes containing group 14 elements as bridging atoms
Materials Chemistry Frontiers, 2018, 2, 929
1553721 CIFC61 H62 Cl2 O12 S4 SnP 1 21/n 19.2728; 21.8232; 27.505
90; 97.123; 90
5523Furukawa, Shunsuke; Hayashi, Keisuke; Yamagishi, Ken; Saito, Masaichi
Synthesis and properties of spiro-type heterasumanenes containing group 14 elements as bridging atoms
Materials Chemistry Frontiers, 2018, 2, 929
1553722 CIFC14 H15 N O4P -15.0788; 10.061; 12.9069
76.261; 80.914; 81.176
627.97Cui, Rong Rong; Lv, Yuan Chao; Zhao, Yong Sheng; Zhao, Na; Li, Nan
Solid-state fluorescent materials based on coumarin derivatives: polymorphism, stimuli-responsive emission, self-assembly and optical waveguides
Materials Chemistry Frontiers, 2018, 2, 910
1553723 CIFC60 H56 O10P 1 21/c 19.1235; 60.8969; 8.8517
90; 93.03; 90
4911.07Nabeya, Kota; Muraoka, Takahiro; Hoshino, Norihisa; Aizawa, Miho; Kajitani, Takashi; Akutagawa, Tomoyuki; Shishido, Atsushi; Fukushima, Takanori; Kinbara, Kazushi
Thermal and optical properties of multiblock macrocycles with hysteretic polymorphic transition
Materials Chemistry Frontiers, 2018, 2, 969
1553724 CIFC22 H23 Cl N2 O0 RuP -110.445; 14.347; 14.407
82.53; 85.3; 74.55
2060.7Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie
Ruthenium-catalyzed meta-selective C‒H sulfonation of azoarenes with arylsulfonyl chlorides
Organic Chemistry Frontiers, 2017, 4, 1145
1553725 CIFC18 H13 Cl N2 O2 SC 1 2/c 134.644; 7.0976; 13.544
90; 98.63; 90
3292.6Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie
Ruthenium-catalyzed meta-selective C–H sulfonation of azoarenes with arylsulfonyl chlorides
Organic Chemistry Frontiers, 2017, 4, 1145
1553726 CIFC16 H15 N O7P 21 21 2111.4884; 11.9792; 20.8251
90; 90; 90
2866Wang, Junliang; Li, Jianneng; Shen, Xianwang; Dong, Cong; Lin, Jun; Wei, Kun
Asymmetric total synthesis of (−)-δ-lycorane
Organic Chemistry Frontiers, 2017, 4, 1149
1553727 CIFC60 H46 N4.5P -113.8813; 14.4392; 23.5317
95.8618; 105.365; 91.4814
4517.3Kimura, Yosuke; Kawajiri, Ikumi; Ueki, Masanori; Morimoto, Takayuki; Nishida, Jun-ichi; Ikeda, Hiroshi; Tanaka, Mirai; Kawase, Takeshi
A new fluorophore displaying remarkable solvatofluorochromism and solid-state light emission, and serving as a turn-on fluorescent sensor for cyanide ions
Organic Chemistry Frontiers, 2017, 4, 743
1553728 CIFC11 H16 F3 N O2 S2C 1 2 111.5; 10.46; 11.413
90; 95.06; 90
1367.5Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553729 CIFC19 H10 F4 O2 SP 21 21 216.6977; 8.1914; 30.513
90; 90; 90
1674.1Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553730 CIFC15 H15 F3 O5 SP 21 21 217.5426; 13.2312; 15.9887
90; 90; 90
1595.6Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553731 CIFC17 H11 F3 N2 O SP 21 21 218.5502; 11.0835; 16.8212
90; 90; 90
1594.1Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553732 CIFC11 H14 Cl2 F3 N O2 S2P 1 21 17.7869; 10.8732; 8.8809
90; 95.062; 90
749Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553733 CIFC13 H20 F3 N O4 S2P 1 21 112.4266; 8.8229; 15.107
90; 105.7; 90
1594.5Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553734 CIFC101 H110 N4 Ni P Pt0.5P -115.566; 15.831; 17.7553
80.813; 89.907; 88.251
4317.2Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro
meso-to-meso PtII-bridged NiII-porphyrin dimers
Organic Chemistry Frontiers, 2017, 4, 767
1553735 CIFC162 H174 Cl10 N8 Ni2 PtP -116.142; 21.227; 22.446
106.1; 92.132; 93.364
7365Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro
meso-to-meso PtII-bridged NiII-porphyrin dimers
Organic Chemistry Frontiers, 2017, 4, 767
1553736 CIFC76 H38 Br N O8P 1 21/n 113.8397; 24.2642; 16.7166
90; 109.444; 90
5293.4Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing
Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R
Organic Chemistry Frontiers, 2017, 4, 750
1553737 CIFC76 H39 N O9P n a 2121.489; 10.179; 22.215
90; 90; 90
4859.2Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing
Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R
Organic Chemistry Frontiers, 2017, 4, 750
1553738 CIFC17 H13 Br N2 O4 SP 1 21/c 117.5147; 7.024; 15.73
90; 114.033; 90
1767.4Pal, Kuntal; Volla, Chandra M. R.
Rhodium-catalyzed denitrogenative transannulation of 1,2,3-triazolyl-carbamates: efficient access to 4-aminooxazolidinones
Organic Chemistry Frontiers, 2017, 4, 1380
1553739 CIFC15 H9 F N2P b c a25.513; 13.881; 6.794
90; 90; 90
2406Panaka, Sangeetha; Trivedi, Rajiv; Sony, T.; Prabhakar, S.; Raju Chowhan, L.
Silver(i) catalyzed intramolecular cyclization of N-(2-(alk-1-yn-1-yl))-1H-tetrazoles leading to the formation of N-cyano-2-substituted indoles under ambient conditions
Org. Chem. Front., 2017, 4, 1574
1553740 CIFC16 H13 N2P b c a25.555; 14.1257; 6.8724
90; 90; 90
2480.8Panaka, Sangeetha; Trivedi, Rajiv; Sony, T.; Prabhakar, S.; Raju Chowhan, L.
Silver(i) catalyzed intramolecular cyclization of N-(2-(alk-1-yn-1-yl))-1H-tetrazoles leading to the formation of N-cyano-2-substituted indoles under ambient conditions
Org. Chem. Front., 2017, 4, 1574
1553741 CIFC19 H22 O3C 1 2/c 128.543; 7.309; 16.361
90; 105.04; 90
3296.3Chang, Wenju; Dai, Jie; Li, Jingfu; Shi, Yuan; Ren, Wenlong; Shi, Yian
A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid
Organic Chemistry Frontiers, 2017, 4, 1074
1553742 CIFC11 H8 N O2 SP 1 21/c 15.69674; 8.92923; 19.6982
90; 94.927; 90
998.3Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert
Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties
Organic Chemistry Frontiers, 2017, 4, 861
1553743 CIFC67.5 H66 Cl3 N O2 SP -114.0225; 15.4902; 15.6494
109.303; 105.791; 106.459
2814.2Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert
Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties
Organic Chemistry Frontiers, 2017, 4, 861
1553744 CIFC84 H108 Si4P -18.2685; 13.793; 17.645
72.588; 88.716; 77.009
1868.8Bettinger, Holger F.; Einholz, Ralf; Göttler, Andreas; Junge, Marc; Sättele, Marie-Sophie; Schnepf, Andreas; Schrenk, Claudio; Schundelmeier, Simon; Speiser, Bernd
6,6′,11,11′-Tetra((triisopropylsilyl)ethynyl)-anti-[2.2](1,4)tetracenophane: a covalently coupled tetracene dimer and its structural, electrochemical, and photophysical characterization
Organic Chemistry Frontiers, 2017, 4, 853
1553745 CIFC14 H14 N2 O2 SP -16.121; 8.835; 13.265
83.14; 79.6; 72.93
672.8Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng
Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis
Organic Chemistry Frontiers, 2017, 4, 1266
1553746 CIFC15 H17 N3 O4 SP 1 21 18.6132; 7.4744; 12.867
90; 109.429; 90
781.2Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng
Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis
Organic Chemistry Frontiers, 2017, 4, 1266
1553747 CIFC30 H24C 1 c 121.7066; 21.7067; 20.1949
90; 122.509; 90
8024.4Takai, Atsuro; Freas, Dylan J.; Suzuki, Toshikane; Sugimoto, Manabu; Labuta, Jan; Haruki, Rie; Kumai, Reiji; Adachi, Shin-ichi; Sakai, Hayato; Hasobe, Taku; Matsushita, Yoshitaka; Takeuchi, Masayuki
The effect of a highly twisted CC double bond on the electronic structures of 9,9′-bifluorenylidene derivatives in the ground and excited states
Organic Chemistry Frontiers, 2017, 4, 650
1553748 CIFC15 H13 N O4 S2P -17.6834; 8.0281; 12.554
85.471; 73.42; 74.044
713.6Zhou, Kaida; Xia, Hongguang; Wu, Jie
Generation of benzosultams via a radical process with the insertion of sulfur dioxide
Organic Chemistry Frontiers, 2017, 4, 1121
1553749 CIFC15 H13 N O4 S2P 1 21/c 18.151; 8.239; 22.94
90; 100.06; 90
1517Zhou, Kaida; Xia, Hongguang; Wu, Jie
Generation of benzosultams via a radical process with the insertion of sulfur dioxide
Organic Chemistry Frontiers, 2017, 4, 1121
1553750 CIFC26 H31 N3 O6P 19.0047; 9.2247; 9.4826
109.875; 108.593; 107.103
626.45Guo, Jing; Lin, Zi-Hui; Chen, Kai-Bin; Xie, Ying; Chan, Albert S. C.; Weng, Jiang; Lu, Gui
Asymmetric amination of 2-substituted indolin-3-ones catalyzed by natural cinchona alkaloids
Organic Chemistry Frontiers, 2017, 4, 1400
1553751 CIFC54 H48 O8P -18.9558; 9.4432; 13.6247
92.926; 95.287; 111
1066.8Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi
Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems
Organic Chemistry Frontiers, 2017, 4, 828
1553752 CIFC66 H72 O6P 1 21/n 111.8673; 14.8352; 15.9367
90; 102.976; 90
2734.08Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi
Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems
Organic Chemistry Frontiers, 2017, 4, 828
1553753 CIFC41 H27 OC 1 2/c 123.6823; 14.1831; 19.4393
90; 101.921; 90
6388.6Ip, Ho-Wang; Chow, Hak-Fun; Kuck, Dietmar
Electronic and steric effects on the three-fold Scholl-type cycloheptatriene ring formation around a tribenzotriquinacene core
Organic Chemistry Frontiers, 2017, 4, 817
1553754 CIFC18 H16 N2 O2P 1 21/c 112.4244; 8.0614; 14.7164
90; 100.607; 90
1448.78Selvaraju, Manikandan; Wang, Ying-Lien; Sun, Chung-Ming
Ruthenium(ii)-catalyzed C–H alkenylation/annulation cascade for the rapid synthesis of benzoimidazoisoindoles
Organic Chemistry Frontiers, 2017, 4, 1358
1553755 CIFC7.75 H7.75 F7.75 N7.75 O7.75 S7.75P 21 21 218.086; 14.196; 23.304
90; 90; 90
2675Pouambeka, Tony Wheellyam; Zhang, Ge; Zheng, Guang-Fan; Xu, Guo-Xing; Zhang, Qian; Xiong, Tao; Zhang, Qian
Copper-catalyzed oxidative amidation of α,β-unsaturated ketones via selective C‒H or C‒C bond cleavage
Organic Chemistry Frontiers, 2017, 4, 1420
1553756 CIFC27 H21 N O2 S2P 21 21 215.9608; 18.7773; 20.3817
90; 90; 90
2281.3Shi, Qing; Li, Pinhua; Zhang, Yan; Wang, Lei
Visible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions
Organic Chemistry Frontiers, 2017, 4, 1322
1553757 CIFC16 H12 Cl N OP 1 21/c 19.0611; 7.1551; 20.5051
90; 93.684; 90
1326.66Zhang, Zhiguo; Zhang, Yongchao; Huang, Guoqing; Zhang, Guisheng
Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles
Organic Chemistry Frontiers, 2017, 4, 1372
1553758 CIFC17 H18 Br F3 N2 O6P 21 21 218.3955; 14.09; 16.7651
90; 90; 90
1983.19Liu, Qiang; Zhao, Kun; Zhi, Ying; Raabe, Gerhard; Enders, Dieter
Squaramide-catalyzed domino Michael/aza-Henry [3 + 2] cycloaddition: asymmetric synthesis of functionalized 5-trifluoromethyl and 3-nitro substituted pyrrolidines
Organic Chemistry Frontiers, 2017, 4, 1416
1553759 CIFC23 H22 Br Cl2 N3 O5P 1 21/n 19.593; 15.307; 16.705
90; 93.785; 90
2447.6Chen, Dong-Zhen; Xiao, Wen-Jing; Chen, Jia-Rong
Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes
Organic Chemistry Frontiers, 2017, 4, 1289

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