Crystallography Open Database

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1554403 CIFC14 H18 N2 O SP -15.5091; 7.2665; 16.992
80.823; 83.934; 78.863
656.9Dutta, Soumya; Mondal, Manas; Ghosh, Tubai; Saha, Amit
Unprecedented thiocarbamidation of nitroarenes: a facile one-pot route to unsymmetrical thioureas
Organic Chemistry Frontiers, 2019, 6, 70
1554419 CIFC20 H18P n a 2115.853; 12.375; 7.3639
90; 90; 90
1444.7Muthuramalingam, Somasundaram; Garg, Jai Anand; Karthick, R.; Fox, Thomas; Blacque, Olivier; Venkatesan, Koushik; Ramanathan, Saiganesh; Kabilan, Senthamaraikannan; Balasubramanian, K. K.
Nickel catalyzed synthesis of 4,4′-bichromenes/4,4′-bithiochromenes and their Atropisomerism
Organic Chemistry Frontiers, 2019, 6, 134
1554420 CIFC20 H14 O4P 1 21/c 18.0844; 19.8817; 10.2123
90; 109.061; 90
1551.44Muthuramalingam, Somasundaram; Garg, Jai Anand; Karthick, R.; Fox, Thomas; Blacque, Olivier; Venkatesan, Koushik; Ramanathan, Saiganesh; Kabilan, Senthamaraikannan; Balasubramanian, K. K.
Nickel catalyzed synthesis of 4,4′-bichromenes/4,4′-bithiochromenes and their Atropisomerism
Organic Chemistry Frontiers, 2019, 6, 134
1554437 CIFC13 H13 N O4 SP 1 21/c 19.1009; 17.5658; 8.1862
90; 103.294; 90
1273.61Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung
Structural assignment of the enol‒keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones
Organic Chemistry Frontiers, 2019, 6, 183
1554438 CIFC13 H15 N O5 SP -17.2268; 9.0737; 10.4696
80.813; 84.674; 88.958
674.8Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung
Structural assignment of the enol‒keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones
Organic Chemistry Frontiers, 2019, 6, 183
1554439 CIFC13 H19 N O8 SP -17.2412; 9.7236; 11.4552
85.64; 87.406; 77.183
783.86Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung
Structural assignment of the enol‒keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones
Organic Chemistry Frontiers, 2019, 6, 183
1554440 CIFC16 H13 N O5 SP 1 21/n 16.6266; 18.2993; 11.8645
90; 99.67; 90
1418.3Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung
Structural assignment of the enol‒keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones
Organic Chemistry Frontiers, 2019, 6, 183
1554446 CIFC31 H44 N3 P2 RhP 1 21/n 110.9778; 16.148; 17.5888
90; 106.231; 90
2993.7Zhou, Chunhui; Hu, Jinsong; Wang, Yuan; Yao, Changguang; Chakraborty, Priyanka; Li, Huaifeng; Guan, Chao; Huang, Mei-Hui; Huang, Kuo-Wei
Selective carbonylation of benzene to benzaldehyde using a phosphorus‒nitrogen PN3P‒rhodium(i) complex
Organic Chemistry Frontiers, 2019, 6, 721
1554447 CIFC92 H120 N6 O3 P4 Rh2C 1 2/c 129.2408; 13.8295; 25.4214
90; 120.925; 90
8818.6Zhou, Chunhui; Hu, Jinsong; Wang, Yuan; Yao, Changguang; Chakraborty, Priyanka; Li, Huaifeng; Guan, Chao; Huang, Mei-Hui; Huang, Kuo-Wei
Selective carbonylation of benzene to benzaldehyde using a phosphorus‒nitrogen PN3P‒rhodium(i) complex
Organic Chemistry Frontiers, 2019, 6, 721
1554449 CIFC30 H37 I N2 RuP -112.2395; 14.363; 18.399
89.442; 89.312; 88.419
3232.9Wu, Xuan-Jun; Wang, Hua-Jing; Yang, Zhao-Qi; Tang, Xiao-Sheng; Yuan, Ye; Su, Wei; Chen, Cheng; Verpoort, Francis
Efficient and phosphine-free bidentate N-heterocyclic carbene/ruthenium catalytic systems for the dehydrogenative amidation of alcohols and amines
Organic Chemistry Frontiers, 2019, 6, 563
1554450 CIFC27 H31 I N2 RuP 1 21/n 115.329; 7.7727; 21.254
90; 95.269; 90
2521.7Wu, Xuan-Jun; Wang, Hua-Jing; Yang, Zhao-Qi; Tang, Xiao-Sheng; Yuan, Ye; Su, Wei; Chen, Cheng; Verpoort, Francis
Efficient and phosphine-free bidentate N-heterocyclic carbene/ruthenium catalytic systems for the dehydrogenative amidation of alcohols and amines
Organic Chemistry Frontiers, 2019, 6, 563
1554463 CIFC27 H25 N O3 SP -18.892; 9.668; 13.91
86.33; 86.29; 67.91
1105Beltran, Frédéric; Andna, Lucile; Miesch, Laurence
Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts
Organic Chemistry Frontiers, 2019, 6, 373
1554464 CIFC22 H25 N O3 SP -17.6023; 7.8229; 16.7412
85.307; 84.129; 85.07
984.06Beltran, Frédéric; Andna, Lucile; Miesch, Laurence
Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts
Organic Chemistry Frontiers, 2019, 6, 373
1554465 CIFC28 H27 N O3 SP 1 21/c 110.5059; 11.5524; 19.3292
90; 99.812; 90
2311.6Beltran, Frédéric; Andna, Lucile; Miesch, Laurence
Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts
Organic Chemistry Frontiers, 2019, 6, 373
1554466 CIFC25 H29 N O3 SP 1 21/n 18.6751; 21.9074; 12.355
90; 107.893; 90
2234.5Beltran, Frédéric; Andna, Lucile; Miesch, Laurence
Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts
Organic Chemistry Frontiers, 2019, 6, 373
1554485 CIFC20 H24 O5P 21 21 216.1036; 12.5506; 21.976
90; 90; 90
1683.45Yang, Qian; Hu, Kun; Yan, Bing-Chao; Liu, Miao; Li, Xiao-Nian; Sun, Han-Dong; Puno, Pema-Tenzin
Maoeriocalysins A‒D, four novel ent-kaurane diterpenoids from Isodon eriocalyx and their structure determination utilizing quantum chemical calculation in conjunction with quantitative interproton distance analysis
Organic Chemistry Frontiers, 2019, 6, 45
1554489 CIFC10 H8 F N3P b c a7.4865; 11.7277; 20.913
90; 90; 90
1836.1Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming
Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives
Organic Chemistry Frontiers, 2019, 6, 426
1554490 CIFC16 H12 F N5 O2P 1 21/c 18.4745; 13.483; 12.5515
90; 96.566; 90
1424.7Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming
Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives
Organic Chemistry Frontiers, 2019, 6, 426
1554491 CIFC10 H8 F N3P 1 21/n 16.185; 7.487; 18.728
90; 96.138; 90
862.3Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming
Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives
Organic Chemistry Frontiers, 2019, 6, 426
1554492 CIFC70 H56 Ag5 Cl2 N6 P4A e a 227.38; 26.9; 24.03
90; 90; 90
17699Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming
Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives
Organic Chemistry Frontiers, 2019, 6, 426
1554493 CIFC20 H14 N2P -13.9188; 12.5127; 15.3057
101.08; 96.416; 92.665
730.13Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong
ReI-Catalyzed highly regio- and stereoselective C‒H addition to terminal and internal alkynes
Organic Chemistry Frontiers, 2019, 6, 432
1554494 CIFC22 H19 N3P 1 21/c 110.5762; 7.8869; 19.9879
90; 91.535; 90
1666.7Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong
ReI-Catalyzed highly regio- and stereoselective C‒H addition to terminal and internal alkynes
Organic Chemistry Frontiers, 2019, 6, 432
1554495 CIFC25 H20 N4 O2P -19.1577; 10.7173; 13.3021
106.893; 91.497; 91.349
1248.12Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong
ReI-Catalyzed highly regio- and stereoselective C‒H addition to terminal and internal alkynes
Organic Chemistry Frontiers, 2019, 6, 432
1554496 CIFC30 H25 N O3P 1 21 18.5256; 16.9053; 8.9274
90; 112.31; 90
1190.37Xu, Jianfeng; Peng, Jingyi; He, Chonglong; Ren, Hongjun
N-Heterocyclic carbene catalyzed chemo- and enantioselective cross-benzoin reaction of aldehydes with isatins
Organic Chemistry Frontiers, 2019, 6, 172
1554497 CIFC18 H12 Cl3 O P S3C 1 2/c 112.268; 8.6753; 37.965
90; 92.878; 90
4035.5Lu, Guozhang; Chen, Jun; Huangfu, Xinlei; Li, Xueyan; Fang, Meijuan; Tang, Guo; Zhao, Yufen
Visible-light-mediated direct synthesis of phosphorotrithioates as potent anti-inflammatory agents from white phosphorus
Organic Chemistry Frontiers, 2019, 6, 190
1554498 CIFC38 H42 Cl2 O7C 1 2 125.2058; 7.2704; 19.2306
90; 105.306; 90
3399.1Fan, Jian-Hong; Hu, Ya-Jian; Guo, Qiang; Li, Shaoping; Zhao, Jing; Li, Chuang-Chuang
Asymmetric synthesis of the tetracyclic core of bufogargarizin C by an intramolecular [5 + 2] cycloaddition
Organic Chemistry Frontiers, 2019, 6, 22
1554499 CIFC27 H22 N O2 PP 1 21 17.8836; 12.2399; 11.1988
90; 90.174; 90
1080.62Zhang, Dong-Liang; Li, Cheng-Kun; Zeng, Run-Sheng; Shoberu, Adedamola; Zou, Jian-Ping
Manganese(iii)-mediated selective phosphorylation of enamides: direct synthesis of β-phosphoryl enamides
Organic Chemistry Frontiers, 2019, 6, 236
1554500 CIFC27 H22 N O2 PP 16.0253; 9.0011; 10.3679
75.005; 76.437; 89.09
527.4Zhang, Dong-Liang; Li, Cheng-Kun; Zeng, Run-Sheng; Shoberu, Adedamola; Zou, Jian-Ping
Manganese(iii)-mediated selective phosphorylation of enamides: direct synthesis of β-phosphoryl enamides
Organic Chemistry Frontiers, 2019, 6, 236
1554501 CIFC19 H15 F3 O4C 1 2/c 123.47; 9.9387; 17.2934
90; 123.484; 90
3364.4Chen, Yueji; You, Yi; Weng, Zhiqiang
Syntheses of 2-(2,2,2-trifluoroethylidene)/(2,2-difluoroethyl)-1,3-dicarbonyl compounds and their fungicidal activities
Organic Chemistry Frontiers, 2019, 6, 213
1554502 CIFC17 H12 Br2 F2 O2P 1 21/c 113.7491; 5.8303; 21.42
90; 105.814; 90
1652.1Chen, Yueji; You, Yi; Weng, Zhiqiang
Syntheses of 2-(2,2,2-trifluoroethylidene)/(2,2-difluoroethyl)-1,3-dicarbonyl compounds and their fungicidal activities
Organic Chemistry Frontiers, 2019, 6, 213
1554503 CIFC22 H21 N O5P 21 21 221.2879; 7.5138; 11.5723
90; 90; 90
1851.02Shoji, Taku; Araki, Takanori; Iida, Nanami; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Okujima, Tetsuo
Synthesis of azulenophthalimides by phosphine-mediated annulation of 1,2-diformylazulenes with maleimides
Organic Chemistry Frontiers, 2019, 6, 195
1554504 CIFC68 H68 Cl6 N4 O10 P2R -3 :H25.2081; 25.2081; 30.11
90; 90; 120
16570Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554505 CIFC66 H66 I N2 O4 P2C 1 2/c 119.7346; 19.9943; 14.9829
90; 110.36; 90
5542.6Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554506 CIFC34 H34 Br Cl3 N O2 PP 1 21/c 110.967; 15.8648; 20.3172
90; 105.084; 90
3413.2Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554507 CIFC66 H66 F6 N2 O4 P3C 1 2/c 119.664; 19.9512; 15.5025
90; 111.125; 90
5673.2Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554508 CIFC66 H66 Cl N2 O7.33 P2R -3 :H24.8062; 24.8062; 30.0418
90; 90; 120
16009.5Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554509 CIFC74 H86 F12 N2 O6 P4P b c a15.5817; 20.6208; 22.0566
90; 90; 90
7086.9Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554510 CIFC66 H66 N2 O4 P2P 1 21/c 114.2234; 15.5567; 12.5242
90; 108.744; 90
2624.2Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554511 CIFC66 H66 Br N2 O4 P2R -3 :H24.7543; 24.7543; 30.0212
90; 90; 120
15931.6Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554512 CIFC12 H17 N SP 1 21/c 16.3585; 10.945; 17.5672
90; 92.051; 90
1221.78Lai, Miao; Wu, Zhiyong; Wang, Yizhi; Zheng, Ying; Zhao, Mingqin
Selective synthesis of aryl thioamides and aryl-α-ketoamides from α-oxocarboxylic acids and tetraalkylthiuram disulfides: an unexpected chemoselectivity from aryl sulfonyl chlorides
Organic Chemistry Frontiers, 2019, 6, 506
1554513 CIFC21 H19 Br O3P 21 21 2110.687; 12.035; 14.902
90; 90; 90
1917Huang, Huicai; Lu, Xue; Mao, Yukang; Ye, Jinxing
Asymmetric synthesis of highly functionalized furanones via direct Michael reactions mediated by a bulky primary amine
Organic Chemistry Frontiers, 2019, 6, 1080
1554514 CIFC17 H20 O3P 21 21 2110.4344; 11.4942; 11.5277
90; 90; 90
1382.58Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang
Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis
Organic Chemistry Frontiers, 2019, 6, 290
1554515 CIFC20 H20 O3P -18.431; 8.6965; 11.7742
80.603; 87.055; 65.92
777.47Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang
Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis
Organic Chemistry Frontiers, 2019, 6, 290
1554516 CIFC25 H21 F O3P 1 21/c 19.8733; 10.3877; 37.781
90; 96.893; 90
3846.8Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang
Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis
Organic Chemistry Frontiers, 2019, 6, 290
1554517 CIFC19 H16 O2F d d 223.63; 42.848; 5.8546
90; 90; 90
5927.8Fan, Jian; Wang, Shengke; Chen, Jiahui; Wu, Manyi; Zhang, Jitan; Xie, Meihua
Synthesis of 2-acetyl trisubstituted furans via copper-mediated deacylation cleavage of unstrained C(sp3)‒C(sp2) bonds
Organic Chemistry Frontiers, 2019, 6, 437
1554518 CIFC20 H18 O3P 1 21/c 110.476; 15.249; 11.317
90; 116.28; 90
1621Fan, Jian; Wang, Shengke; Chen, Jiahui; Wu, Manyi; Zhang, Jitan; Xie, Meihua
Synthesis of 2-acetyl trisubstituted furans via copper-mediated deacylation cleavage of unstrained C(sp3)‒C(sp2) bonds
Organic Chemistry Frontiers, 2019, 6, 437
1554519 CIFC23 H21 N O3 SI 1 a 18.3257; 15.1988; 16.3404
90; 95.005; 90
2059.8Zhu, Tong-Hao; Zhang, Xiao-Chen; Zhao, Kai; Loh, Teck-Peng
Cu(OTf)2-mediated C(sp2)‒H arylsulfonylation of enamides via the insertion of sulfur dioxide
Organic Chemistry Frontiers, 2019, 6, 94
1554520 CIFC23 H25 N3 O3P 21 21 2111.8106; 12.5767; 26.9924
90; 90; 90
4009.4Luo, Xiaowei; Chen, Chunmei; Tao, Huaming; Lin, Xiuping; Yang, Bin; Zhou, Xuefeng; Liu, Yonghong
Structurally diverse diketopiperazine alkaloids from the marine-derived fungus Aspergillus versicolor SCSIO 41016
Organic Chemistry Frontiers, 2019, 6, 736
1554521 CIFC20 H23 N2 O3 PP -19.115; 9.448; 11.944
101.46; 91.031; 106.62
962.9Yang, Qiaolan; Wu, Chenglin; Zhou, Jianhui; He, Guoxue; Liu, Hong; Zhou, Yu
Highly selective C‒H bond activation of N-arylbenzimidamide and divergent couplings with diazophosphonate compounds: a catalyst-controlled selective synthetic strategy for 3-phosphorylindoles and 4-phosphorylisoquinolines
Organic Chemistry Frontiers, 2019, 6, 393
1554522 CIFC18 H20 N O3 PP 1 c 17.6453; 11.642; 9.808
90; 102.969; 90
850.7Yang, Qiaolan; Wu, Chenglin; Zhou, Jianhui; He, Guoxue; Liu, Hong; Zhou, Yu
Highly selective C‒H bond activation of N-arylbenzimidamide and divergent couplings with diazophosphonate compounds: a catalyst-controlled selective synthetic strategy for 3-phosphorylindoles and 4-phosphorylisoquinolines
Organic Chemistry Frontiers, 2019, 6, 393
1554523 CIFC30 H40 N6 O12C 1 2/c 127.337; 6.1593; 20.343
90; 106.22; 90
3288.9Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel
Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water
Organic Chemistry Frontiers, 2019, 6, 75
1554524 CIFC30 H36 N6 O10P 1 21/n 16.8698; 14.4541; 14.7842
90; 95.204; 90
1461.97Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel
Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water
Organic Chemistry Frontiers, 2019, 6, 75
1554525 CIFC26 H38 N6 O9 S2P n a 2115.1627; 6.4915; 29.4057
90; 90; 90
2894.4Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel
Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water
Organic Chemistry Frontiers, 2019, 6, 75
1554526 CIFC21 H28 N2 O8P 1 21 111.4833; 7.3773; 13.116
90; 96.533; 90
1103.92Ma, Qiaoning; Yang, Xiaodi; Lei, Xinsheng; Lin, Guo-Qiang
A highly enantioselective synthetic method towards the α2c-adrenoceptor antagonist ORM-10921
Organic Chemistry Frontiers, 2019, 6, 773
1554527 CIFC32 H34 Br0 Cl N O4P 21 21 216.1903; 13.744; 32.103
90; 90; 90
2731.3Ma, Qiaoning; Yang, Xiaodi; Lei, Xinsheng; Lin, Guo-Qiang
A highly enantioselective synthetic method towards the α2c-adrenoceptor antagonist ORM-10921
Organic Chemistry Frontiers, 2019, 6, 773
1554528 CIFC5 H4 F N5 O6P -17.976; 8.218; 15.344
94.059; 104.85; 97.364
958.5Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.
N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design
Organic Chemistry Frontiers, 2019, 6, 249
1554529 CIFC5 H4 F N5 O6P 1 21 15.4659; 10.477; 8.1322
90; 94.857; 90
464.03Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.
N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design
Organic Chemistry Frontiers, 2019, 6, 249
1554530 CIFC3 H3 F N6 O4P n a 2111.4331; 5.7212; 11.2434
90; 90; 90
735.44Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.
N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design
Organic Chemistry Frontiers, 2019, 6, 249
1554531 CIFC5 H4 F N5 O6P b c a6.6055; 11.5186; 23.4809
90; 90; 90
1786.57Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.
N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design
Organic Chemistry Frontiers, 2019, 6, 249
1554532 CIFC19 H15 N O3P c a 2114.3845; 4.3448; 23.199
90; 90; 90
1449.9Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung
Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides
Organic Chemistry Frontiers, 2019, 6, 226
1554533 CIFC19 H15 N O2P 1 c 121.0827; 8.2829; 8.2169
90; 95.222; 90
1428.93Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung
Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides
Organic Chemistry Frontiers, 2019, 6, 226
1554534 CIFC28 H33 Au Cl O2 PP -19.2179; 10.4777; 14.2247
100.062; 92.031; 103.287
1312.41Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung
Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides
Organic Chemistry Frontiers, 2019, 6, 226
1554535 CIFC33 H32 Cl N O9P 21 21 2111.0158; 12.13; 23.587
90; 90; 90
3151.7Cao, Jian; Liu, Jin-Yu; Zhang, Yi-Ming; Wang, Zhu-Yin; Xu, Peng-Fei
Synergistic promotion by intramolecular hydrogen bonding: a bi-functionally catalyzed cascade reaction for the synthesis of enantiopure chromenopyrrolidines
Organic Chemistry Frontiers, 2019, 6, 674
1554536 CIFC20 H15 Br2 N O2P c a 217.0667; 23.0878; 21.9663
90; 90; 90
3583.9Liu, Zhenhua; Zhu, Guangyu; Gao, Wen; Yang, Lin; Ji, Huimin; Tong, Lili; Tang, Bo
Copper-catalyzed regioselective cyclization of vinyl azides by gem-difluoromethylene for trisubstituted pyridines
Organic Chemistry Frontiers, 2019, 6, 468
1554537 CIFC17 H17 Br N4 OP -15.2572; 12.458; 13.205
69.94; 83.57; 89.74
806.7Lemport, Pavel S.; Smolyar, Ivan V.; Khrustalev, Victor N.; Roznyatovsky, Vitaly A.; Popov, Alexander V.; Kobelevskaya, Valentina A.; Rozentsveig, Igor B.; Nenajdenko, Valentine G.
3,3-Diazidoenones ‒ new types of highly reactive bis-azides. Preparation and synthetic transformations
Organic Chemistry Frontiers, 2019, 6, 335
1554538 CIFC27 H21 N2 O PP 1 21/c 112.429; 10.415; 37.841
90; 90.13; 90
4898.4Lemport, Pavel S.; Smolyar, Ivan V.; Khrustalev, Victor N.; Roznyatovsky, Vitaly A.; Popov, Alexander V.; Kobelevskaya, Valentina A.; Rozentsveig, Igor B.; Nenajdenko, Valentine G.
3,3-Diazidoenones ‒ new types of highly reactive bis-azides. Preparation and synthetic transformations
Organic Chemistry Frontiers, 2019, 6, 335
1554539 CIFC34 H44 N2 O SiP -18.8134; 10.3559; 18.035
100.993; 95.022; 92.933
1605.78Chen, Cui-Hong; Chai, Yun; Zhou, Zheng-Xin; Rao, Wei-Hao; Liu, Bin; Liu, Li; Xu, Ran; Liu, Yue-Jin; Zeng, Ming-Hua
Room-temperature Pd(ii)-catalyzed direct C‒H TIPS-ethynylation of phenylacetic amides with terminal alkynes
Organic Chemistry Frontiers, 2019, 6, 442
1554540 CIFC35 H30P m n 2144.902; 11.1591; 10.6337
90; 90; 90
5328.2Liu, Peiren; Li, Qi; Zeng, Hong; Shi, Bingbing; Liu, Jiyong; Huang, Feihe
[15]Paracyclophane and [16]paracyclophane: facile syntheses, crystal structures and selective complexation with cesium cations in the gas phase
Organic Chemistry Frontiers, 2019, 6, 309
1554541 CIFC42 H36P -111.372; 13.1796; 24.509
105.144; 93.375; 90.36
3538.8Liu, Peiren; Li, Qi; Zeng, Hong; Shi, Bingbing; Liu, Jiyong; Huang, Feihe
[15]Paracyclophane and [16]paracyclophane: facile syntheses, crystal structures and selective complexation with cesium cations in the gas phase
Organic Chemistry Frontiers, 2019, 6, 309
1554542 CIFC42 H54 O6 S2 SeP -114.2625; 18.0213; 31.3062
86.466; 83.674; 83.298
7933.2Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng
Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity
Organic Chemistry Frontiers, 2019, 6, 263
1554543 CIFC42 H54 O8 S2 SeP 1 21/n 117.4194; 8.2052; 28.3968
90; 90.166; 90
4058.73Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng
Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity
Organic Chemistry Frontiers, 2019, 6, 263
1554544 CIFC42 H54 O6 Se Te2P -112.1441; 16.8305; 20.8669
98.844; 91.448; 102.981
4098.7Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng
Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity
Organic Chemistry Frontiers, 2019, 6, 263
1554545 CIFC42 H54 O6 S Se2P -114.2879; 18.0394; 31.4094
86.414; 83.365; 83.373
7977.7Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng
Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity
Organic Chemistry Frontiers, 2019, 6, 263
1554546 CIFC24 H19 Br N2 OP 1 21/c 113.0718; 15.5471; 10.5005
90; 113.181; 90
1961.7Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554547 CIFC24 H19 Cl N2 OP 1 21/c 112.9966; 15.5319; 10.522
90; 113.397; 90
1949.3Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554548 CIFC16 H14 Cl N O2P 21 21 219.5976; 10.3316; 13.9249
90; 90; 90
1380.8Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554549 CIFC19 H16 N2 OP -18.802; 9.9463; 10.213
116.522; 100.853; 103.243
734.13Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554550 CIFC19 H19 Cl2 N O4C 1 2/c 133.58; 13.96; 8.0737
90; 100.506; 90
3721.3Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554551 CIFC13 H22 O2P b c a11.8513; 8.0917; 24.6768
90; 90; 90
2366.4He, Min; Yi, Jiuzhou; Zhao, Gaoyuan; Chen, Peiqi; Long, Dan; Hu, Xiaojun; Li, Huilin; Xie, Xingang; Wang, Xiaolei; She, Xuegong
A concise approach to the tricyclic framework of longipinane- and ent-longipinane-type sesquiterpenoids
Organic Chemistry Frontiers, 2019, 6, 383
1554552 CIFC25 H24 O5 SP 1 21 19.1789; 10.574; 11.4116
90; 91.684; 90
1107.11Zhang, Nan; He, Tingting; Liu, Yidong; Li, Shan; Tan, Yu; Peng, Lei; Li, Dongmei; Shan, Chunhui; Yan, Hailong
Organocatalytic atropo- and E/Z-selective Michael addition reaction of ynones with α-amido sulfones as sulfone-type nucleophile
Organic Chemistry Frontiers, 2019, 6, 451
1554553 CIFC12 H10 F3 N O6 SeP -19.809; 9.877; 9.925
66.084; 65.463; 64.347
758.1Ge, Hangming; Shen, Qilong
Trifluoromethyl-substituted selenium ylide: a broadly applicable electrophilic trifluoromethylating reagent
Organic Chemistry Frontiers, 2019, 6, 2205
1554554 CIFC20 H29 N O SP 1 21 110.5315; 7.0899; 12.4878
90; 105.29; 90
899.43Qin, Shuanglin; Liu, Tongtong; Luo, Yunhao; Jiang, Shende; Yang, Guang
Diastereoselective Rh-catalyzed decarboxylative allylation to form quaternary stereocenters using sulfinimine as the directing group
Organic Chemistry Frontiers, 2019, 6, 732
1554555 CIFC26 H31 N3 SiC 1 2/c 141.982; 8.4505; 16.3226
90; 123.085; 90
4851.8Wu, Wanqing; Fang, Songjia; Jiang, Guangbin; Li, Meng; Jiang, Huanfeng
Palladium-catalyzed regioselective C‒H alkynylation of indoles with bromoalkynes in water
Organic Chemistry Frontiers, 2019, 6, 2200
1554556 CIFC30 H25 N O2P 1 21/c 15.7768; 26.401; 15.2336
90; 95.248; 90
2313.6Ji, Cheng-Long; Pan, Yao; Geng, Fang-Zhou; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Synergistic silver/scandium catalytic spiroketalization of β-alkynyl ketones for the atom economical synthesis of skeletally diverse spirocyclic isochromenes
Organic Chemistry Frontiers, 2019, 6, 474
1554557 CIFC21 H21 N O2 SC 1 2/c 131.1655; 8.4946; 13.3472
90; 98.752; 90
3492.37Wu, Feng; Chen, Lianfen; Wang, Yongdong; Zhu, Shifa
Gold-catalyzed generation of azafulvenium from an enyne sulfonamide: rapid access to fully substituted pyrroles
Organic Chemistry Frontiers, 2019, 6, 480
1554558 CIFC21 H18 Br N O3 SP 1 21/n 18.6549; 18.21; 11.9124
90; 94.769; 90
1870.96Wu, Feng; Chen, Lianfen; Wang, Yongdong; Zhu, Shifa
Gold-catalyzed generation of azafulvenium from an enyne sulfonamide: rapid access to fully substituted pyrroles
Organic Chemistry Frontiers, 2019, 6, 480
1554559 CIFC28 H36 N2 O2 SiP -19.7904; 10.7882; 12.3517
83.891; 69.723; 84.499
1214.36Kong, De-Shen; Wang, Yi-Fan; Tan, Yun-Xuan; Zhang, Jun-Li; Zhang, Jian-Ge; Tian, Ping; Lin, Guo-Qiang
Trisannulation of benzamides and cyclohexadienone-tethered 1,1-disubstituted allenes initiated by Cp*Rh(iii)-catalyzed C‒H activation
Organic Chemistry Frontiers, 2019, 6, 699
1554560 CIFC27 H31 N O4 SiP -19.9601; 10.6766; 11.8691
74.393; 85.571; 88.958
1211.99Kong, De-Shen; Wang, Yi-Fan; Tan, Yun-Xuan; Zhang, Jun-Li; Zhang, Jian-Ge; Tian, Ping; Lin, Guo-Qiang
Trisannulation of benzamides and cyclohexadienone-tethered 1,1-disubstituted allenes initiated by Cp*Rh(iii)-catalyzed C‒H activation
Organic Chemistry Frontiers, 2019, 6, 699
1554561 CIFC31 H26 Cl2 N4 O4 S2P 1 21/c 18.24; 10.3859; 17.7438
90; 95.373; 90
1511.84Han, Shuaijun; Gao, Xianying; Wu, Qingsong; Li, Jingya; Zou, Dapeng; Wu, Yusheng; Wu, Yangjie
Nickel-promoted C(2)‒H amidation of quinoline N-oxides with N-fluorobenzenesulfonimide
Organic Chemistry Frontiers, 2019, 6, 830
1554562 CIFC25.5 H28 Cl N4 O2.5 PdP n a 2125.795; 9.144; 21.256
90; 90; 90
5013.6Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin
Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides
Organic Chemistry Frontiers, 2019, 6, 544
1554563 CIFC18 H11 Br N2C 1 2/c 126.203; 10.644; 30.852
90; 106.633; 90
8245Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin
Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)‒H and C(sp3)‒H bonds of carboxamides
Organic Chemistry Frontiers, 2019, 6, 544
1554564 CIFC16 H18 O2 SP 1 21 15.712; 15.28; 8.28
90; 104.192; 90
700.6Sun, Yongjie; Jiang, Jun; Guo, Xiaochong; Wen, Jialin; Zhang, Xumu
Asymmetric hydrogenation of α,β-unsaturated sulfones by a rhodium/thiourea‒bisphosphine complex
Organic Chemistry Frontiers, 2019, 6, 1438
1554565 CIFC32 H27 N O4 SP 43 21 213.6813; 13.6813; 29.053
90; 90; 90
5438.1Chen, Kun-Quan; Gao, Zhong-Hua; Ye, Song
Bifunctional N-heterocyclic carbene catalyzed [3 + 4] annulation of enals with azadienes: enantioselective synthesis of benzofuroazepinones
Organic Chemistry Frontiers, 2019, 6, 405
1554566 CIFC33 H29 N O4 SP 21 21 2111.043; 14.753; 17.258
90; 90; 90
2811.6Chen, Kun-Quan; Gao, Zhong-Hua; Ye, Song
Bifunctional N-heterocyclic carbene catalyzed [3 + 4] annulation of enals with azadienes: enantioselective synthesis of benzofuroazepinones
Organic Chemistry Frontiers, 2019, 6, 405
1554567 CIFC22 H24 O7P -19.1375; 13.1527; 16.354
95.187; 95.294; 103.04
1894.04Liu, Hongxin; Tan, Haibo; Wang, Wenxuan; Zhang, Wenge; Chen, Yuchan; Li, Saini; Liu, Zhaoming; Li, Haohua; Zhang, Weimin
Cytorhizophins A and B, benzophenone-hemiterpene adducts from the endophytic fungus Cytospora rhizophorae
Organic Chemistry Frontiers, 2019, 6, 591
1554568 CIFC18 H17 Cl3 O5P 1 2 113.8718; 9.6965; 13.8978
90; 92.204; 90
1867.98Liu, Hongxin; Tan, Haibo; Wang, Wenxuan; Zhang, Wenge; Chen, Yuchan; Li, Saini; Liu, Zhaoming; Li, Haohua; Zhang, Weimin
Cytorhizophins A and B, benzophenone-hemiterpene adducts from the endophytic fungus Cytospora rhizophorae
Organic Chemistry Frontiers, 2019, 6, 591
1554569 CIFC172 H203 N13 O10 P2C 1 2/c 121.469; 29.096; 28.543
90; 95.17; 90
17757Lee, Chaeeun; Lee, Hyemi; Lee, Seungwon; Jeon, Hae-Geun; Jeong, Kyu-Sung
Encapsulation of dihydrogenphosphate ions as a cyclic dimer to the cavities of site-specifically modified indolocarbazole-pyridine foldamers
Organic Chemistry Frontiers, 2019, 6, 299
1554570 CIFC173 H203 N13 O10 P2C 1 2/c 121.505; 29.114; 28.751
90; 94.83; 90
17937Lee, Chaeeun; Lee, Hyemi; Lee, Seungwon; Jeon, Hae-Geun; Jeong, Kyu-Sung
Encapsulation of dihydrogenphosphate ions as a cyclic dimer to the cavities of site-specifically modified indolocarbazole-pyridine foldamers
Organic Chemistry Frontiers, 2019, 6, 299
1554571 CIFC12 H12 N2 O2 SP 1 21/c 18.968; 9.084; 14.804
90; 105.357; 90
1163Zu, Weisai; Liu, Shuai; Jia, Xin; Xu, Liang
Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan‒Evans‒Lam reactions
Organic Chemistry Frontiers, 2019, 6, 1356
1554572 CIFC19 H15 N O2 SP 1 21 18.0275; 8.0254; 12.699
90; 101.787; 90
800.9Zhao, Zi-Biao; Shi, Lei; Meng, Fan-Jie; Li, Yaming; Zhou, Yong-Gui
Synthesis of chiral seven-membered cyclic sulfonamides through palladium-catalyzed arylation of cyclic imines
Organic Chemistry Frontiers, 2019, 6, 1572
1554573 CIFC10 H13 N O3P 16.9308; 6.9507; 11.8464
84.194; 79.023; 64.094
503.84Yang, Wu-Lin; Sun, Zhong-Tao; Zhang, Jian; Li, Zhong; Deng, Wei-Ping
Enantioselective synthesis of 3-amino-hydrobenzofuran-2,5-diones via Cu(i)-catalyzed intramolecular conjugate addition of imino esters
Organic Chemistry Frontiers, 2019, 6, 579
1554574 CIFC116 H162 Br F3 O12P 1 21 115.1538; 13.5668; 27.2737
90; 92.794; 90
5600.5Al-Azemi, Talal F.; Vinodh, Mickey; Alipour, Fatemeh H.; Mohamod, Abdirahman A.
Chiral discrimination of 2-heptlyaminium salt by planar-chiral monohydroxy-functionalized pillar[5]arenes
Organic Chemistry Frontiers, 2019, 6, 603
1554575 CIFC116 H162 Br F3 O12P 1 21 115.0627; 13.3599; 27.1554
90; 94.396; 90
5448.6Al-Azemi, Talal F.; Vinodh, Mickey; Alipour, Fatemeh H.; Mohamod, Abdirahman A.
Chiral discrimination of 2-heptlyaminium salt by planar-chiral monohydroxy-functionalized pillar[5]arenes
Organic Chemistry Frontiers, 2019, 6, 603
1554576 CIFC10 H8 N2 SeP 1 21/c 17.15; 11.643; 12.098
90; 95.268; 90
1002.9Cao, Yuan; Liu, Jie; Liu, Fanmin; Jiang, Lvqi; Yi, Wenbin
Copper-catalyzed direct and odorless selenylation with a sodium selenite-based reagent
Organic Chemistry Frontiers, 2019, 6, 825
1554577 CIFC9 H9 F3 N2P 1 21 15.799; 7.486; 10.479
90; 104.17; 90
441.1Chen, Mu-Wang; Deng, Zhihong; Yang, Qin; Huang, Jian; Peng, Yiyuan
Enantioselective synthesis of trifluoromethylated dihydroquinoxalinones via palladium-catalyzed hydrogenation
Organic Chemistry Frontiers, 2019, 6, 746
1554578 CIFC29 H24 N2 O2P 21 21 219.1297; 10.326; 24.127
90; 90; 90
2274.5Xu, Lubin; Chen, Haohua; Liu, Jian; Zhou, Lan; Liu, Qing; Lan, Yu; Xiao, Jian
Chiral phosphoric acid-catalyzed asymmetric C(sp3)‒H functionalization of biomass-derived 2,5-dimethylfuran via two sequential Cope-type rearrangements
Organic Chemistry Frontiers, 2019, 6, 1162
1554579 CIFC9.23 H13.23 O3.69P 21 21 2132.1461; 11.483; 8.0162
90; 90; 90
2959.05Zhang, Jia; He, Jun; Cheng, Yung-Chi; Zhang, Pei-Cheng; Yan, Yu; Zhang, Hao-Jun; Zhang, Wei-Ku; Xu, Jie-Kun
Fischernolides A‒D, four novel diterpene-based meroterpenoid scaffolds with antitumor activities from Euphorbia fischeriana
Organic Chemistry Frontiers, 2019, 6, 2312
1554580 CIFC35 H26 Cl N5 OP 21 21 2111.351; 11.9996; 21.215
90; 90; 90
2889.6Sun, Bing-Bing; Zhang, Jun-Qi; Chen, Jun-Bo; Fan, Wei-Tai; Yu, Jie-Qiang; Hu, Jia-Ming; Wang, Xing-Wang
Stereoselective synthesis of spirocyclohexadiene-pyrazolones via organic base and/or hydrogen bonding assisted [3 + 3] annulation reactions
Organic Chemistry Frontiers, 2019, 6, 1842
1554581 CIFC33 H23 Cl N4 OP -19.3289; 10.9229; 12.8668
87.237; 78.614; 85.681
1280.91Sun, Bing-Bing; Zhang, Jun-Qi; Chen, Jun-Bo; Fan, Wei-Tai; Yu, Jie-Qiang; Hu, Jia-Ming; Wang, Xing-Wang
Stereoselective synthesis of spirocyclohexadiene-pyrazolones via organic base and/or hydrogen bonding assisted [3 + 3] annulation reactions
Organic Chemistry Frontiers, 2019, 6, 1842
1554582 CIFC16 H14 F3 N O4 SP 21 21 217.9193; 15.3744; 16.4929
90; 90; 90
2008.08Gui, Yang; Liang, Xinping; Li, Yanan; Li, Kuiliang; Zha, Zhenggen; Wang, Zhiyong
Asymmetric synthesis of fluoroalkylated N,O-ketals via an organocatalytic dehydration/aminalization/aza-Michael desymmetrization
Organic Chemistry Frontiers, 2019, 6, 942
1554583 CIFC36 H32 Br N O4 P2P 21 21 2128.168; 11.3424; 10.2126
90; 90; 90
3262.9Liu, Bing; Li, Wenbo; Wu, Hai-Hong; Zhang, Junliang
Enantiodivergent synthesis of 1,2-bis(diphenylphosphino)ethanes via asymmetric [3 + 2]-cycloaddition
Organic Chemistry Frontiers, 2019, 6, 694
1554584 CIFC22 H20 Br N3 O4P 1 21 19.2282; 9.1743; 12.829
90; 109.724; 90
1022.4Xie, Chao-Chao; Tan, Rui; Liu, Yan-Kai
Asymmetric construction of polycyclic indole derivatives with different ring connectivities by an organocatalysis triggered two-step sequence
Organic Chemistry Frontiers, 2019, 6, 919
1554585 CIFC21 H24 N2 O7P 1 21 19.6264; 10.858; 11.2163
90; 113.736; 90
1073.2Xie, Chao-Chao; Tan, Rui; Liu, Yan-Kai
Asymmetric construction of polycyclic indole derivatives with different ring connectivities by an organocatalysis triggered two-step sequence
Organic Chemistry Frontiers, 2019, 6, 919
1554586 CIFC17 H20 F3 N O3P 1 21/c 111.431; 5.931; 25.849
90; 94.751; 90
1746.5Gupta, Ekta; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor
Additive-free regio- and diastereoselective construction of fully-substituted isoxazolidines employing diazo compounds
Organic Chemistry Frontiers, 2019, 6, 1109
1554587 CIFC14 H14 F3 N O2P -111.218; 12.296; 16.82
108.32; 101.98; 102.65
2051.1Gupta, Ekta; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor
Additive-free regio- and diastereoselective construction of fully-substituted isoxazolidines employing diazo compounds
Organic Chemistry Frontiers, 2019, 6, 1109
1554694 CIFC260 H202 Cu4 N16 O23P 1 21/n 138.372; 43.842; 41.771
90; 101.834; 90
68778Maehara, Takeshi; Sekiya, Ryo; Harada, Kentaro; Haino, Takeharu
Tunable enforced cavities inside self-assembled capsules
Organic Chemistry Frontiers, 2019, 6, 1561
1554695 CIFC40 H40 B Cl4 Cu F4 N4P -110.7588; 13.1415; 15.339
106.956; 100.938; 91.717
2028.3Maehara, Takeshi; Sekiya, Ryo; Harada, Kentaro; Haino, Takeharu
Tunable enforced cavities inside self-assembled capsules
Organic Chemistry Frontiers, 2019, 6, 1561
1554696 CIFC31 H29 Cl N2 O4P 21 21 219.0064; 9.7885; 30.9078
90; 90; 90
2724.81Chu, Ming-Ming; Qi, Suo-Suo; Ju, Wan-Zhen; Wang, Yi-Feng; Chen, Xue-Yang; Xu, Dan-Qian; Xu, Zhen-Yuan
Asymmetric organocatalytic conjugated addition of pyrazolin-5-ones to ortho-quinomethanes: construction of vicinal tertiary and all-carbon quaternary stereocenters
Organic Chemistry Frontiers, 2019, 6, 1140
1554697 CIFC63.5 H60 N6 O14.5C 1 c 136.594; 7.353; 28.802
90; 123.87; 90
6435Ren, Demin; Liu, Bin; Li, Xiaofang; Koniarz, Sebastian; Pawlicki, Miłosz; Chmielewski, Piotr J.
Reactions of 2-aza-21-carbaporphyrin with aniline derivatives
Organic Chemistry Frontiers, 2019, 6, 908
1554698 CIFC79 H72 N6 O6P 1 21/c 133.74; 12.9479; 14.8229
90; 100.325; 90
6370.7Ren, Demin; Liu, Bin; Li, Xiaofang; Koniarz, Sebastian; Pawlicki, Miłosz; Chmielewski, Piotr J.
Reactions of 2-aza-21-carbaporphyrin with aniline derivatives
Organic Chemistry Frontiers, 2019, 6, 908
1554699 CIFC18 H16 Br2 F N O3 SP -16.9921; 11.2113; 12.4434
96.443; 95.376; 95.626
959.19Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554700 CIFC19 H20 Cl N O3 SC 1 2/c 118.258; 13.081; 15.4466
90; 91.845; 90
3687.2Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554701 CIFC17 H14 N2 O7 SP 1 21/n 17.4466; 24.7338; 9.6421
90; 104.56; 90
1718.87Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554702 CIFC21 H25 N O4 SP -110.994; 12.052; 16.9
95.131; 99.76; 103.107
2130Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554703 CIFC17 H16 Br3 N O2 SP 1 21/c 18.2985; 12.4303; 19.4432
90; 101.322; 90
1966.59Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554704 CIFC17 H14 Br3 N O3 SP -16.9458; 10.9848; 12.6203
95.166; 94.677; 97.68
946.11Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554705 CIFC16 H11 F3 N2 OP 1 21/c 16.5927; 24.4163; 9.1339
90; 108.268; 90
1396.18Zhu, Chuanle; Liu, Chi; Zeng, Hao; Chen, Fulin; Jiang, Huanfeng
Transition-metal free selective C(α)‒C(β) bond cleavage of trifluoromethyl ketones with amidines under air: facile access to 5-trifluoromethylated Imidazol-4-ones
Organic Chemistry Frontiers, 2019, 6, 858
1554706 CIFC21 H22 Cl N5 O8C 1 2 125.9456; 8.8451; 23.3704
90; 101.146; 90
5262.1Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming
Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes
Organic Chemistry Frontiers, 2019, 6, 863
1554707 CIFC22 H26 Cl N5 O9P 1 21/c 114.6444; 19.027; 9.2992
90; 98.115; 90
2565.17Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming
Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes
Organic Chemistry Frontiers, 2019, 6, 863
1554708 CIFC25 H22 Cl N5 O8P -18.9522; 12.3288; 12.6211
103.938; 101.104; 102.417
1275.71Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming
Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes
Organic Chemistry Frontiers, 2019, 6, 863
1554709 CIFC21 H23 Br N2 O4 SP 21 21 219.4007; 10.8468; 21.7267
90; 90; 90
2215.42Shen, Guoli; Khan, Ruhima; Lv, Haiping; Yang, Yong; Zhang, Xia; Zhan, Yong; Zhou, Yongyun; Fan, Baomin
Palladium/silver co-catalyzed syn-stereoselective asymmetric ring-opening reactions of azabenzonorbornadienes with amides
Organic Chemistry Frontiers, 2019, 6, 1423
1554710 CIFC14 H8 F2 S2P 1 21/c 17.4893; 3.8493; 19.835
90; 94.273; 90
570.23Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554711 CIFC12 H6 F N2 S2P 1 21/n 15.9315; 4.9497; 18.794
90; 95.89; 90
548.86Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554712 CIFC12 H6 F2 N2 S2P 1 21/n 15.7427; 5.5541; 17.1753
90; 90.509; 90
547.79Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554713 CIFC14 H6 F4 S2P 1 21/n 16.2999; 5.0655; 18.6515
90; 90.341; 90
595.2Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554714 CIFC30 H46 F N2 S2 Si2P 1 21/c 19.3302; 12.3529; 14.5826
90; 106.185; 90
1614.11Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554715 CIFC30 H48 N2 S2 Si2P 1 21/c 19.2882; 12.3511; 14.5307
90; 105.826; 90
1603.77Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554716 CIFC12 H4 F4 N2 S2P -15.0225; 7.1949; 17.29
84.549; 83.096; 70.873
584.99Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554717 CIFC30 H46 F2 N2 S2 Si2P 1 21/c 19.3622; 12.3591; 14.6437
90; 106.674; 90
1623.15Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554718 CIFC12 H5 F N2 S2P 1 21/c 13.8093; 6.6644; 21.5126
90; 94.338; 90
544.57Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554719 CIFC30 H44 F4 N2 S2 Si2P n a 2119.9633; 12.2859; 13.3676
90; 90; 90
3278.6Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554720 CIFC12 H6 F2 N2 S2P 1 21/n 16.6214; 25.6046; 7.2049
90; 116.456; 90
1093.59Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554721 CIFC12 H4 F4 N2 S2P 1 21/n 13.8531; 23.868; 6.121
90; 95.29; 90
560.53Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554722 CIFC12 H8 N2 S2F d d 215.9825; 9.7302; 13.6524
90; 90; 90
2123.12Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554723 CIFC29 H28 O2P -110.2239; 11.009; 11.0538
73.729; 86.05; 65.798
1087.85Zhang, He; Cao, Tongxiang; Luo, Hejiang; Chen, Lianfen; Zhu, Shifa
Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes
Organic Chemistry Frontiers, 2019, 6, 1118
1554724 CIFC26 H20 O3P 1 21/n 111.5269; 6.9766; 23.812
90; 98.369; 90
1894.54Zhang, He; Cao, Tongxiang; Luo, Hejiang; Chen, Lianfen; Zhu, Shifa
Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes
Organic Chemistry Frontiers, 2019, 6, 1118
1554725 CIFC76 H32 F8 O8C 1 2/c 122.035; 15.426; 17.593
90; 121.518; 90
5098Ma, Yue; Uchiyama, Kouya; Ueno, Hiroshi; Okada, Hiroshi; Moriyama, Hiroshi; Matsuo, Yutaka
Highly soluble C2v-symmetrical fullerene derivatives: efficient synthesis, characterization, and electrochemical study
Organic Chemistry Frontiers, 2019, 6, 1372
1554726 CIFC76 H16 Cl24 O8P 1 21/n 121.782; 13.957; 24.511
90; 110.66; 90
6972.41Ma, Yue; Uchiyama, Kouya; Ueno, Hiroshi; Okada, Hiroshi; Moriyama, Hiroshi; Matsuo, Yutaka
Highly soluble C2v-symmetrical fullerene derivatives: efficient synthesis, characterization, and electrochemical study
Organic Chemistry Frontiers, 2019, 6, 1372
1554727 CIFC15 H18 Br N O4P 21 21 215.0429; 11.88; 25.83
90; 90; 90
1547.5Hu, Hui-Juan; Chen, Peng; Ao, Yu-Fei; Wang, Qi-Qiang; Wang, De-Xian; Wang, Mei-Xiang
Highly efficient biocatalytic desymmetrization of meso carbocyclic 1,3-dicarboxamides: a versatile route for enantiopure 1,3-disubstituted cyclohexanes and cyclopentanes
Organic Chemistry Frontiers, 2019, 6, 808
1554728 CIFC15 H18 Br N O4P 21 21 216.5631; 12.796; 18.385
90; 90; 90
1544Hu, Hui-Juan; Chen, Peng; Ao, Yu-Fei; Wang, Qi-Qiang; Wang, De-Xian; Wang, Mei-Xiang
Highly efficient biocatalytic desymmetrization of meso carbocyclic 1,3-dicarboxamides: a versatile route for enantiopure 1,3-disubstituted cyclohexanes and cyclopentanes
Organic Chemistry Frontiers, 2019, 6, 808
1554729 CIFC20 H17 O2 PC 1 c 116.191; 17.7337; 8.5986
90; 137.72; 90
1661Zhao, Xiuli; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Wu, Yangjie
Stepwise photosensitized C(sp3)‒C(CO) bond cleavage and C‒P bond formation of 1,3-dicarbonyls with arylphosphine oxides
Organic Chemistry Frontiers, 2019, 6, 1433
1554730 CIFC34 H25 Cl O2P -112.1117; 15.5259; 21.575
95.307; 97.116; 101.212
3920.6Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554731 CIFC32 H20 N2 O6P 1 21/n 110.7141; 20.1653; 12.3094
90; 107.329; 90
2538.8Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554732 CIFC32 H21 Br O2P 1 21/c 110.602; 20.505; 12.2951
90; 114.94; 90
2423.6Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554733 CIFC26 H19 Cl OP -19.998; 15.063; 15.716
63.252; 83.527; 76.536
2055Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554734 CIFC34 H25 Br O4P 1 21/n 113.3814; 10.6318; 19.2274
90; 92.604; 90
2732.6Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554735 CIFC32 H33 Cl3 N4 Ni O4P 19.3743; 13.379; 14.9327
81.008; 89.658; 80.276
1822.85Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I.
A general synthesis of unnatural α-amino acids by iron-catalysed olefin‒olefin coupling via generated radicals
Organic Chemistry Frontiers, 2019, 6, 1094
1554736 CIFC18.5 H19.5 N1.5 Ni0.5 O2P 1 21 19.846; 12.0451; 14.2648
90; 110.181; 90
1587.89Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I.
A general synthesis of unnatural α-amino acids by iron-catalysed olefin‒olefin coupling via generated radicals
Organic Chemistry Frontiers, 2019, 6, 1094
1554737 CIFC36 H39 Cl4 N3 Ni O3P 21 21 2111.452; 13.8346; 22.8016
90; 90; 90
3612.5Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I.
A general synthesis of unnatural α-amino acids by iron-catalysed olefin‒olefin coupling via generated radicals
Organic Chemistry Frontiers, 2019, 6, 1094
1554738 CIFC24 H27 Br O3P 21 21 215.459; 7.8884; 51.7461
90; 90; 90
2228.33Xin, Xiaodong; Pan, Xinhui; Meng, Zhilin; Liu, Xigong; Liu, Lei
Catalytic enantioselective cross-dehydrogenative coupling of 3,6-dihydro-2H-pyrans with aldehydes
Organic Chemistry Frontiers, 2019, 6, 1448
1554739 CIFC23 H19 Br N2 O3 SP 1 21/c 112.1948; 18.8246; 10.1822
90; 105.486; 90
2252.6Xu, Ze-Feng; Shan, Lihong; Zhang, Wan; Cen, Mengjie; Li, Chuan-Ying
Synthesis of α-aminoketones from N-sulfonyl-1,2,3-triazoles via N-sulfinyl imines generated by intramolecular oxygen transfer
Organic Chemistry Frontiers, 2019, 6, 1391
1554740 CIFC43 H36 N4 O9C 2 2 2117.41181; 27.6471; 17.61491
90; 90; 90
8479.57Liu, Xiong-Li; Gong, Yi; Chen, Shuang; Zuo, Xiong; Yao, Zhen; Zhou, Ying
Bifunctional oxindole-chromone 4C building block directed asymmetric synthesis of bispirocyclic hexahydroxanthones featuring five contiguous stereocenters and two side-by-side oxindoles
Organic Chemistry Frontiers, 2019, 6, 1603
1554741 CIFC40 H37.5 N4 O9C 1 2 129.1304; 17.2687; 17.7328
90; 103.665; 90
8667.88Liu, Xiong-Li; Gong, Yi; Chen, Shuang; Zuo, Xiong; Yao, Zhen; Zhou, Ying
Bifunctional oxindole-chromone 4C building block directed asymmetric synthesis of bispirocyclic hexahydroxanthones featuring five contiguous stereocenters and two side-by-side oxindoles
Organic Chemistry Frontiers, 2019, 6, 1603
1554742 CIFC31 H26 Cl2 HfP 1 21/m 18.1722; 16.0848; 9.1272
90; 95.0903; 90
1195.02Amaya, Toru; Katoh, Shun; Moriuchi, Toshiyuki; Hirao, Toshikazu
Synthesis of a sumanenyl hafnocene complex
Organic Chemistry Frontiers, 2019, 6, 1032
1554743 CIFC24 H34 O6P 1 21 17.272; 12.369; 12.296
90; 105.99; 90
1063.2Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei
Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate
Organic Chemistry Frontiers, 2019, 6, 868
1554744 CIFC30 H43 N O7P 6517.407; 17.407; 17.977
90; 90; 120
4717.3Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei
Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate
Organic Chemistry Frontiers, 2019, 6, 868
1554745 CIFC24 H34 O5P 1 21 17.323; 12.384; 12.233
90; 106.42; 90
1064.1Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei
Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate
Organic Chemistry Frontiers, 2019, 6, 868
1554746 CIFC28 H35 N O3P 21 21 2110.391; 12.429; 18.269
90; 90; 90
2359.4Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei
Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate
Organic Chemistry Frontiers, 2019, 6, 868
1554747 CIFC25 H17 Cl3 N2 O2 SP 1 21/c 113.0109; 11.5329; 16.1284
90; 109.629; 90
2279.5Wang, Shengzheng; Guo, Zhongjie; Wu, Ying; Liu, Wei; Liu, Xueying; Zhang, Shengyong; Sheng, Chunquan
Organocatalytic asymmetric synthesis of highly functionalized spiro-thiazolone‒cyclopropane-oxindoles bearing two vicinal spiro quaternary centers
Organic Chemistry Frontiers, 2019, 6, 1442
1554748 CIFC40 H34 I3 N3P 41 21 213.41045; 13.41045; 40.0935
90; 90; 90
7210.42Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A.
Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands
Organic Chemistry Frontiers, 2019, 6, 1226
1554749 CIFC152 H120 B4 F16 N8 Pd2P 42 21 232.9899; 32.9899; 14.3593
90; 90; 90
15627.7Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A.
Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands
Organic Chemistry Frontiers, 2019, 6, 1226
1554750 CIFC280 H248 F24 N8 O27 P8 Pd4 S8C 1 2/c 146.6905; 26.3232; 31.9982
90; 97.75; 90
38968Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A.
Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands
Organic Chemistry Frontiers, 2019, 6, 1226
1554751 CIFC62 H74 N22 Na O21 S2P -112.4931; 18.1989; 20.9673
89.537; 87.89; 72.498
4543.3Bauer, Daniel; Andrae, Beatrice; Gaß, Patrick; Trenz, Danjano; Becker, Sabine; Kubik, Stefan
Functionalisable acyclic cucurbiturils
Organic Chemistry Frontiers, 2019, 6, 1555
1554752 CIFC64 H72 Cl2 N18 Na2 O19 S2P b c n19.1042; 43.808; 23.0275
90; 90; 90
19272.1Bauer, Daniel; Andrae, Beatrice; Gaß, Patrick; Trenz, Danjano; Becker, Sabine; Kubik, Stefan
Functionalisable acyclic cucurbiturils
Organic Chemistry Frontiers, 2019, 6, 1555
1554754 CIFC108 H150 F12 N2 O18 P2P 1 21/n 117.6358; 25.0174; 26.064
90; 109.616; 90
10832.1Li, Dong-Hao; Yang, Liu-Pan; Chai, Hongxin; Jia, Fei; Ke, Hua; Jiang, Wei
Temperature-induced large amplitude conformational change in the complex of oxatub[4]arene revealed via rotaxane synthesis
Organic Chemistry Frontiers, 2019, 6, 1027
1554757 CIFC19 H11 F5 N2 O2P 1 21/c 112.1293; 8.5068; 15.8667
90; 92.925; 90
1635.02Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C‒H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554758 CIFC19 H20 N4 O3P -17.886; 9.5658; 11.4661
86.429; 79.097; 77.958
830.42Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C‒H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554759 CIFC21 H16 Cl N3 O3P -18.0444; 10.7234; 11.5467
71.104; 70.41; 73.474
870.38Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C‒H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554760 CIFC19 H20 N4 O3P -17.7358; 9.6039; 11.631
85.647; 76.146; 78.816
822.65Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C‒H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554761 CIFC22 H19 N3 O4P 1 21/c 18.7562; 23.4732; 8.8632
90; 92.21; 90
1820.35Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C‒H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554762 CIFC21 H15 Cl F N3 O3P 1 21/c 17.3959; 19.3566; 12.7098
90; 91.147; 90
1819.2Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C‒H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554763 CIFC29 H19 F6 N3 O4P 1 21/c 115.9357; 13.7866; 11.8725
90; 93.908; 90
2602.3Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C‒H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554766 CIFC60 H78 Cl2 N4 O16P -115.267; 19.087; 24.39
87.94; 83.839; 73.08
6760Jordan, Jacobs H.; Wishard, Anthony; Mague, Joel T.; Gibb, Bruce C.
Binding properties and supramolecular polymerization of a water-soluble resorcin[4]arene
Organic Chemistry Frontiers, 2019, 6, 1236
1554768 CIFC6.21 H2.28 Cl0.48 N0.07 O0.28 S0P -19.9983; 16.3521; 19.4651
102.163; 90.869; 105.091
2995.41Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554769 CIFC143 H54 N2 O10 S2P 1 21/n 110.4701; 25.097; 16.2566
90; 91.218; 90
4270.8Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554770 CIFC70 H22.75 N O4.88 S2C 1 c 114.4203; 27.3088; 10.3569
90; 94.182; 90
4067.7Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554771 CIFC81 H42.7 N O5.85 S2P -110.4366; 16.3952; 16.824
110.869; 99.019; 100.619
2565.14Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554772 CIFC143 H57.4 N2 O11.7 S2P 1 21/n 110.4595; 25.0584; 16.2556
90; 91.316; 90
4259.4Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554775 CIFC19 H20 N2 SeP 1 21/c 113.3462; 10.2259; 12.0633
90; 96.466; 90
1635.89Guo, Tao; Wei, Xu-Ning; Liu, Yu; Zhang, Pan-Ke; Zhao, Yun-Hui
Oxidative dual C‒H selenation of imidazoheterocycles with ethers or alkanes using selenium powder via a radical pathway
Organic Chemistry Frontiers, 2019, 6, 1414
1554777 CIFC21 H18 N O3 PP 21 21 218.4621; 19.7458; 21.2129
90; 90; 90
3544.5Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554778 CIFC25 H23 N2 O2 PP 1 21/n 118.5757; 6.176; 18.9148
90; 98.809; 90
2144.38Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554779 CIFC22.5 H14.5 Cl1.5 F3 N2 O2 PC 1 2/c 129.394; 6.3419; 28.119
90; 121.188; 90
4484.2Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554780 CIFC21 H15 N2 O2 PC 1 2/c 124.331; 10.2408; 14.54
90; 102.686; 90
3534.5Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554781 CIFC21 H15 N2 O2 PC 1 2/c 126.4131; 9.7872; 14.9148
90; 115.7; 90
3474.22Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554784 CIFC13 H18 N2 O2 S2P b c a14.1538; 10.7714; 20.0319
90; 90; 90
3054Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos ‒ precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554785 CIFC11 H12 O4 S2P -15.1535; 7.3073; 16.2864
81.694; 82.41; 74.561
582.16Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos ‒ precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554786 CIFC36 H38 O2 S2C 1 c 119.6986; 10.9502; 16.5805
90; 122.988; 90
2999.9Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos ‒ precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554787 CIFC40 H46 O2 S2P -19.4599; 10.4995; 17.9405
82.254; 86.522; 88.292
1762Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos ‒ precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554788 CIFC41 H48 O2 S2P 1 21/n 111.3446; 17.747; 17.3945
90; 97.039; 90
3475.7Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos ‒ precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554789 CIFC13 H18 N2 O2 S2P 1 21/c 110.5966; 11.0075; 13.0168
90; 103.286; 90
1477.67Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos ‒ precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244

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