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
1554790 CIFC37 H40 O2 S2P 1 21/c 114.4032; 9.233; 24.7181
90; 93.6338; 90		3280.5Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos ‒ precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554792 CIFC24 H12 F6 SeP 1 21/c 112.234; 10.9831; 14.6454
90; 111.492; 90		1831Shi, Xinzhe; Mao, Shuxin; Roisnel, Thierry; Doucet, Henri; Soulé, Jean-François
Palladium-catalyzed successive C‒H bond arylations and annulations toward the π-extension of selenophene-containing aromatic skeletons
Organic Chemistry Frontiers, 2019, 6, 2398
1554795 CIFC36 H23 Br F3 N2 O3P 21 21 2111.6434; 14.186; 17.6525
90; 90; 90		2915.72Li, Boyu; Gao, Fengyun; Feng, Xing; Sun, Mengmeng; Guo, Yifei; Wen, Dongwa; Deng, Yabo; Huang, Jinqi; Wang, Kairong; Yan, Wenjin
Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole-pyrrolidine]s through organocatalytic cycloaddition
Organic Chemistry Frontiers, 2019, 6, 1567
1554799 CIFC27 H40 O6P 1 21 19.8327; 16.984; 16.2007
90; 101.138; 90		2654.54Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui
The absolute configurations of hyperilongenols A‒C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
Organic Chemistry Frontiers, 2019, 6, 1491
1554800 CIFC29 H44 O6P 21 21 2112.0011; 13.3921; 17.7454
90; 90; 90		2852.04Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui
The absolute configurations of hyperilongenols A‒C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
Organic Chemistry Frontiers, 2019, 6, 1491
1554801 CIFC26 H38 O6P 1 21 19.6691; 16.4235; 15.94
90; 101.09; 90		2484.01Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui
The absolute configurations of hyperilongenols A‒C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
Organic Chemistry Frontiers, 2019, 6, 1491
1554805 CIFC162 H174 Au4 Cl16 O8 P4P -112.983; 13.401; 29.22
81.31; 77.62; 61.97		4376Hau, Franky Ka-Wah; Cheung, Kai-Leung; Zhu, Nianyong; Yam, Vivian Wing-Wah
Calixarene-based alkynyl-bridged gold(i) isocyanide and phosphine complexes as building motifs for the construction of chemosensors and supramolecular architectures
Organic Chemistry Frontiers, 2019, 6, 1205
1554807 CIFC27 H23 N OP -110.4979; 10.7112; 10.8365
60.7986; 76.2796; 71.3801		1003.08Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy
Organic Chemistry Frontiers, 2019, 6, 1655
1554808 CIFC27 H23 N OP 1 21 16.7344; 18.9552; 15.1244
90; 90.856; 90		1930.4Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy
Organic Chemistry Frontiers, 2019, 6, 1655
1554811 CIFC34 H30 N2 O7P 21 21 219.7212; 10.3208; 28.5171
90; 90; 90		2861.14Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying
A bifunctional pyrazolone‒chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones
Organic Chemistry Frontiers, 2019, 6, 1485
1554812 CIFC36 H32 F N3 O7P 1 21 111.7466; 12.2636; 22.7319
90; 93.091; 90		3269.89Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying
A bifunctional pyrazolone‒chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones
Organic Chemistry Frontiers, 2019, 6, 1485
1554816 CIFC17 H16 Br F3 O2P 1 21 16.2353; 7.7873; 17.3098
90; 90.759; 90		840.42Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554817 CIFC23 H21 N O7 SP 1 21 110.6202; 6.377; 16.3385
90; 98.252; 90		1095.07Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554818 CIFC18 H17 F3 O3P 21 21 216.4981; 15.2542; 17.146
90; 90; 90		1699.57Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554819 CIFC24 H31 Ag F6 N2 P2P 1 c 115.277; 8.0788; 21.7171
90; 98.481; 90		2651.01Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554820 CIFC31 H41 Ag F6 N4 P2P 1 21/c 112.7111; 17.36; 15.7081
90; 105.588; 90		3338.73Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554821 CIFC25 H31 Ag F3 N2 O PP 1 21/c 111.3702; 12.6386; 17.83
90; 103.361; 90		2492.88Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554823 CIFC27 H40 O4P 21 21 218.061; 10.8588; 27.7356
90; 90; 90		2427.77Xu, Hou-Chao; Hu, Kun; Shi, Xiao-Huo; Tang, Jian-Wei; Li, Xiao-Nian; Sun, Han-Dong; Puno, Pema-Tenzin
Synergistic use of NMR computation and quantitative interproton distance analysis in the structural determination of neokadcoccitane A, a rearranged triterpenoid featuring an aromatic ring D from Kadsura coccinea
Organic Chemistry Frontiers, 2019, 6, 1619
1554825 CIFC15 H13 N3P -15.4882; 11.1825; 11.6413
62.292; 80.059; 76.727		613.82Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554826 CIFC17 H17 N3 O2C 1 2/c 115.105; 12.8664; 15.5822
90; 91.952; 90		3026.6Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554827 CIFC19 H17 B F2 N4 O2P -17.1859; 12.0427; 12.0895
93.791; 100.927; 98.538		1011.05Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554828 CIFC17 H16 N3 O2.5P 1 21/c 110.668; 24.498; 11.286
90; 93.034; 90		2945.4Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554829 CIFC17.14 H14.5 B F2 N3 O2P 1 21/c 111.1306; 11.7622; 24.0194
90; 91.217; 90		3143.92Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554836 CIFC22 H26 N4 O5P 21 21 219.5782; 11.765; 20.2153
90; 90; 90		2278.01Dai, Chuan; Ma, Jun; Li, Min; Wu, Wen; Xia, Xuefeng; Zhang, Jinqiang
Diversity-oriented submonomer synthesis of azapeptides mediated by the Mitsunobu reaction
Organic Chemistry Frontiers, 2019, 6, 2529
1554843 CIFC16 H23 Cl F6 N3 O2 PC 1 c 110.7226; 12.3939; 15.6108
90; 92.991; 90		2071.77Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554844 CIFC17 H23 Cl2 F6 N2 O2 PP 1 21/c 111.8795; 14.5176; 12.6593
90; 102.138; 90		2134.44Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554845 CIFC28 H41 F6 N4 O2 PC 1 2/c 136.485; 10.158; 16.856
90; 92.44; 90		6241Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554846 CIFC34 H49 F12 N7 O4 P2I 1 2/a 124.915; 8.8562; 19.8464
90; 105.666; 90		4216.5Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554847 CIFC26 H39.5 F9 N4.5 O5 P SP -110.7516; 12.0558; 14.8348
107.62; 93.413; 109.731		1696.8Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554848 CIFC19 H29 Cl F6 N3 O2 PP 1 21/n 17.59057; 26.3895; 12.488
90; 107.133; 90		2390.48Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554849 CIFC21 H32 F6 N4 O2 PP 1 21/c 112.3903; 16.1931; 13.6174
90; 113.783; 90		2500.1Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554850 CIFC16 H23 F12 N3 O2 P2P 1 21/n 110.5891; 16.2883; 13.903
90; 102.985; 90		2336.65Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554851 CIFC26 H41 Cl2 F6 N2 O2 PP 1 21/c 118.6093; 10.778; 15.4265
90; 101.706; 90		3029.76Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554852 CIFC30.33 H52.53 Cl2.12 F6 N3 O2.44 PP -19.5322; 18.6061; 21.1198
83.275; 88.086; 80.993		3673.7Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554853 CIFC22 H35 Cl F6 N3 O2 PP 1 21/n 112.7678; 11.6389; 36.278
90; 94.051; 90		5377.6Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554854 CIFC33 H47.66 F12 N6.5 O4.08 P2P -112.1931; 15.3991; 22.7102
95.65; 102.392; 94.7722		4120.61Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554857 CIFC19 H20 O3 SP -16.9512; 8.6039; 15.1128
102.337; 92.466; 108.002		833.95He, Fu-Sheng; Wu, Youqian; Li, Xiaofang; Xia, Hongguang; Wu, Jie
Photoredox-catalyzed sulfonylation of alkenylcyclobutanols with the insertion of sulfur dioxide through semipinacol rearrangement
Organic Chemistry Frontiers, 2019, 6, 1873
1554859 CIFC17 H23 N O5 SP 1 21/n 16.0877; 10.8073; 26.052
90; 93.948; 90		1709.9Xu, Dongyang; Wei, Hongbo; Zhen, Yanxia; Gao, Yu-Qi; Li, Ruoxin; Li, Xingzhou; He, Yupeng; Zhang, Zhong; Xie, Weiqing
Carboxylate phosphabetaine as a bifunctional organocatalyst for the intramolecular ring opening of oxetane
Organic Chemistry Frontiers, 2019, 6, 1681
1554861 CIFC9 H11 B0.75 O2.25P 1 21/n 16.4968; 22.26; 7.1909
90; 116.2; 90		933.1Bhavanarushi, Sangepu; Xu, Yin; Khan, Imran; Luo, Zhibin; Liu, Bin; Xie, Jimin
Transition-metal-free borylation of propargylic alcohols: structurally variable synthesis in ionic liquid medium
Organic Chemistry Frontiers, 2019, 6, 1895
1554863 CIFC11 H7 F3 N2 O2P 1 21/n 15.41; 17.433; 11.237
90; 93.29; 90		1058Peng, Xiaofeng; Zhang, Xiaofei; Li, Shunyao; Lu, Yunfu; Lan, Lefu; Yang, Chunhao
Silver-mediated synthesis of novel 3-CF3/CN/phosphonate-substituted pyrazoles as pyrrolomycin analogues from 3-formylchromones and diazo compounds
Organic Chemistry Frontiers, 2019, 6, 1775
1554865 CIFC24 H22 N2 O9 SP 21 21 2112.2161; 12.5468; 16.7879
90; 90; 90		2573.13Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong
Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes
Organic Chemistry Frontiers, 2019, 6, 1891
1554866 CIFC24 H24 O6P 1 21/c 110.3133; 11.2328; 19.0954
90; 99.604; 90		2181.14Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong
Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes
Organic Chemistry Frontiers, 2019, 6, 1891
1554868 CIFC24 H19 Cl N2 O3P 21 21 215.9309; 17.47; 19.675
90; 90; 90		2038.6Chu, Ming-Ming; Qi, Suo-Suo; Wang, Yi-Feng; Wang, Biao; Jiang, Zhen-Hui; Xu, Dan-Qian; Xu, Zhen-Yuan
Organocatalytic asymmetric [4 + 1] annulation of in situ generated ortho-quinomethanes with 4-halo pyrazolones: straightforward access to chiral spiro-benzofuran pyrazolones
Organic Chemistry Frontiers, 2019, 6, 1977
1554870 CIFC19 H18 N2 O4P 1 21/c 19.3579; 12.566; 29.371
90; 96.6; 90		3430.9Zhang, Wei; Zheng, Han-Liang; Liu, Yang; Yu, Ao; Yang, Chen; Li, Xin; Cheng, Jin-Pei
Catalyst-free amination of α-cyanoarylacetates enabled by single-electron transfer
Organic Chemistry Frontiers, 2019, 6, 1900
1554872 CIFC28 H29 N3 O4P 1 21 17.807; 15.9924; 10.5193
90; 109.003; 90		1241.79Zhang, Yan-Ping; You, Yong; Zhao, Jian-Qiang; Zhou, Xiao-Jian; Zhang, Xiao-Mei; Xu, Xiao-Ying; Yuan, Wei-Cheng
A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of α,β-unsaturated 7-azaindoline amides and azomethine ylides
Organic Chemistry Frontiers, 2019, 6, 1879
1554874 CIFC23 H30 O8P 21 21 218.0029; 15.3468; 17.8042
90; 90; 90		2186.69Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong
Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018
Organic Chemistry Frontiers, 2019, 6, 3053
1554876 CIFC29 H27 N2 O4.5C 1 c 114.3037; 14.0845; 23.7866
90; 91.922; 90		4789.36Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong
Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018
Organic Chemistry Frontiers, 2019, 6, 3053
1554879 CIFC28.33333 H40.33333 N O9.33333P 21 21 218.09067; 25.4976; 41.3088
90; 90; 90		8521.7Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong
Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018
Organic Chemistry Frontiers, 2019, 6, 3053
1554881 CIFC17 H23 N O4P 1 21/c 112.0924; 16.7422; 8.278
90; 107.825; 90		1595.5Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554882 CIFC14 H13 F3 O5P -16.4241; 10.1906; 11.3167
68.951; 83.144; 83.818		684.79Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554883 CIFC17 H20 O4P 1 21/c 112.1636; 10.2486; 12.3402
90; 110.011; 90		1445.5Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554884 CIFC16 H18 O4P 1 21/c 17.6075; 9.2096; 19.424
90; 98.561; 90		1345.7Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554886 CIFC33 H27 Cl3 N2 O5 SP 21 21 2110.9357; 11.7723; 24.8931
90; 90; 90		3204.7Ren, Xiao-Rui; Lin, Jun-Bing; Hu, Xiu-Qin; Xu, Peng-Fei
Bifunctional Brønsted base catalyzed inverse-electron-demand aza-Diels‒Alder reactions of saccharin-derived 1-azadienes with azlactones
Organic Chemistry Frontiers, 2019, 6, 2280
1554888 CIFC3.33 H3 N0.33 O0.33 Se0.33P 1 21/c 15.4632; 16.8139; 10.7302
90; 98.574; 90		974.64Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua
Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates
Organic Chemistry Frontiers, 2019, 6, 1967
1554889 CIFC3.43 H4.71 N0.14 O0.43 Se0.14P 1 21 110.1323; 7.4394; 15.4852
90; 100.787; 90		1146.62Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua
Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates
Organic Chemistry Frontiers, 2019, 6, 1967
1554891 CIFC21 H21 Cl O5P 21 21 217.229; 11.212; 22.921
90; 90; 90		1857.8Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai
Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways
Organic Chemistry Frontiers, 2019, 6, 1972
1554892 CIFC20 H18 O4P 1 21 110.3231; 8.3376; 10.651
90; 116.926; 90		817.35Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai
Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways
Organic Chemistry Frontiers, 2019, 6, 1972
1554893 CIFC21 H19 Cl O4P 21 21 2110.5134; 7.5193; 22.921
90; 90; 90		1812Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai
Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways
Organic Chemistry Frontiers, 2019, 6, 1972
1554895 CIFC16 H15 N3 O4 SP 1 21/n 114.05; 8.3338; 14.2852
90; 101.509; 90		1639Wang, Guodong; Sun, Jian; Wang, Kai; Han, Junfen; Li, Hongshuang; Duan, Guiyun; You, Guirong; Li, Furong; Xia, Chengcai
Palladium-catalyzed direct C‒H nitration and intramolecular C‒H functionalization for the synthesis of 3-nitro-1-(phenylsulfonyl)-1H-indazole derivatives
Organic Chemistry Frontiers, 2019, 6, 1608
1554897 CIFC16 H19 N O3P 1 21 17.9218; 6.5193; 13.434
90; 101.58; 90		679.67Mandzhulo, Aleksandr; Vashchenko, Iryna; Gerasov, Andrii; Vovk, Mykhaylo; Rusanov, Eduard; Fetyukhin, Volodymyr; Lukin, Oleg; Shivanyuk, Alexander
Selective synthesis of N-protected exo-spiro[oxirane-3,2′-tropanes]
Organic Chemistry Frontiers, 2019, 6, 1692
1554899 CIFC24 H36 O3P 21 21 218.9194; 12.8315; 18.5057
90; 90; 90		2118Zhao, Nan; Xie, Shengling; Tian, Peilin; Tong, Rongbiao; Ning, Chengqing; Xu, Jing
Asymmetric total synthesis of (+)-astellatol and (−)-astellatene
Organic Chemistry Frontiers, 2019, 6, 2014
1554901 CIFC20 H30 O4P 21 21 219.9964; 10.5385; 17.4587
90; 90; 90		1839.22Zhang, Jing; Tang, Xuli; Han, Xiao; Feng, Danqing; Luo, Xiangchao; Ofwegen, Leen van; Li, Pinglin; Li, Guoqiang
Sarcoglaucins A-I, new antifouling cembrane-type diterpenes from the South China Sea soft coral Sarcophyton glaucum
Organic Chemistry Frontiers, 2019, 6, 2004
1554903 CIFC19 H20 N2 O3P 1 21 16.5666; 16.4713; 8.0376
90; 111.405; 90		809.39Wang, Bo; Wang, Yuankai; Wang, Zixuan; Wang, Jianbo
Rh(i)-Catalyzed intramolecular [2 + 2 + 1] cycloaddition of diynes with the N-terminal of the diazo group
Organic Chemistry Frontiers, 2019, 6, 2329
1554905 CIFC45 H42 F4 O7C 1 2/c 115.1446; 24.455; 20.982
90; 93.45; 90		7756.8Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R.
Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight
Organic Chemistry Frontiers, 2019, 6, 1961
1554906 CIFC47 H45 F4 O7P -111.4709; 13.897; 14.895
107.986; 112.427; 96.387		2015.5Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R.
Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight
Organic Chemistry Frontiers, 2019, 6, 1961
1554908 CIFC24 H19 N OP 1 21/c 110.273; 10.178; 16.954
90; 99.61; 90		1747.8Zhao, Hong-Ping; Ma, Xiao-Pan; Nie, Shu-Min; Xiao, Yuhong; Mo, Dong-Liang
Synthesis of chromeno[4,3-b]quinolines and spirobenzofuran-3,3′-quinolines through silver-mediated Appel reaction/C‒Br bond cleavage/double selective rearrangement sequence
Organic Chemistry Frontiers, 2019, 6, 2334
1554910 CIFC30 H21 N O2P 1 21/n 110.5982; 10.2369; 20.9415
90; 99.629; 90		2240Wang, Jian; Cai, Panyuan; He, Yimiao; Liu, Yuan; Zhong, Ling; Ding, Shumin; Shang, Yongjia
Tuneable access to isoquinolines via a transition-metal-free C(sp3)‒C(sp3) bond cleavage rearrangement reaction
Organic Chemistry Frontiers, 2019, 6, 2430
1554911 CIFC27 H29 F6 N2 O P RuP -110.7138; 10.8978; 12.099
92.748; 96.702; 90.476		1401.24Hong, Xi; Zhou, Quan; Huang, Shuang; Cui, He-Zhen; Li, Zhi-Ming; Hou, Xiu-Feng
Transition metal catalysed C7 and ortho-selective halogenation of 2-arylbenzo[d]oxazoles
Organic Chemistry Frontiers, 2019, 6, 2226
1554913 CIFC14 H12 N2 OP 21 21 216.8959; 7.1261; 24.02
90; 90; 90		1180.4Feng, Guang-Shou; Zhao, Zi-Biao; Shi, Lei; Zhou, Yong-Gui
Iridium-catalyzed asymmetric hydrogenation of quinazolinones
Organic Chemistry Frontiers, 2019, 6, 2250
1554918 CIFC35 H27 Br F3 N3 O3P 21 21 218.4795; 18.0358; 21.5437
90; 90; 90		3294.78Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing
Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts
Organic Chemistry Frontiers, 2019, 6, 1989
1554919 CIFC40 H31 Cl2 F4 N2 O3P 21 21 2111.9726; 16.0021; 18.2529
90; 90; 90		3497.01Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing
Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts
Organic Chemistry Frontiers, 2019, 6, 1989
1554922 CIFC31 H28 N2 O5P n a 2121.4324; 13.5256; 8.8733
90; 90; 90		2572.2Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei
Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes
Organic Chemistry Frontiers, 2019, 6, 2415
1554923 CIFC30 H25 N3 O3P -18.9859; 10.004; 15.8029
97.57; 90.211; 115.564		1267.4Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei
Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes
Organic Chemistry Frontiers, 2019, 6, 2415
1554925 CIFC38 H31 Br Cl3 N3 O4P 21 21 219.1965; 9.694; 38.3086
90; 90; 90		3415.2Zhang, Jing; Chan, Wai-Lun; Chen, Ligong; Ullah, Nisar; Lu, Yixin
Creation of bispiro[pyrazolone-3,3′-oxindoles] via a phosphine-catalyzed enantioselective [3 + 2] annulation of the Morita‒Baylis‒Hillman carbonates with pyrazoloneyldiene oxindoles
Organic Chemistry Frontiers, 2019, 6, 2210
1554927 CIFC16 H18 OR 3 :H20.961; 20.961; 7.086
90; 90; 120		2696.2Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong
Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F
Organic Chemistry Frontiers, 2019, 6, 2771
1554928 CIFC27 H34 O3 SiC 1 2/c 142.742; 10.4771; 10.9037
90; 93.609; 90		4873.1Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong
Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F
Organic Chemistry Frontiers, 2019, 6, 2771
1554929 CIFC14 H18 O5P -17.3423; 8.4321; 10.4623
85.681; 85.985; 78.332		631.55Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong
Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F
Organic Chemistry Frontiers, 2019, 6, 2771
1554931 CIFC18 H19 N O4 SP b c a17.4772; 10.488; 19.6463
90; 90; 90		3601.2Huang, Guofei; Ren, Xiaoyu; Jiang, Chunhui; Wu, Jia-Hong; Gao, Guowei; Wang, Tianli
Efficient synthesis of (E)-2-nitromethylcinnamates via phosphine-catalyzed tandem α-addition and 1,3-rearrangement
Organic Chemistry Frontiers, 2019, 6, 2872
1554933 CIFC10 H8 N2 SP n a 2115.971; 4.2214; 13.319
90; 90; 90		898Peng, Yingyuan; He, Qian; Zhang, Xiaofei; Yang, Chunhao
Pd-Catalyzed intramolecular C‒H activation and C‒S formation to synthesize pyrazolo[5,1-b]benzothiazoles without an additional oxidant
Organic Chemistry Frontiers, 2019, 6, 3234
1554936 CIFC20 H21 N3 O4P 1 21/n 110.8238; 10.3557; 17.8199
90; 96.908; 90		1982.9Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei
Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates
Organic Chemistry Frontiers, 2019, 6, 3321
1554938 CIFC20 H21 N3 O4P 42 b c21.7832; 21.7832; 8.49552
90; 90; 90		4031.19Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei
Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates
Organic Chemistry Frontiers, 2019, 6, 3321
1554939 CIFC15 H13 N3 O2P -16.9944; 7.8586; 26.1858
85.696; 89.837; 79.658		1411.87Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei
Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates
Organic Chemistry Frontiers, 2019, 6, 3321
1554940 CIFC22 H18 F3 N O3P 21 21 219.69927; 10.835; 16.94975
90; 90; 90		1781.28Rabasa-Alcañiz, Fernando; Hammerl, Daniel; Sánchez-Merino, Anabel; Tejero, Tomás; Merino, Pedro; Fustero, Santos; del Pozo, Carlos
Asymmetric synthesis of polycyclic 3-fluoroalkylproline derivatives by intramolecular azomethine ylide cycloaddition
Organic Chemistry Frontiers, 2019, 6, 2916
1554942 CIFC26 H20 Cu F6 PP b c n15.5529; 7.3629; 19.8862
90; 90; 90		2277.26Liu, He; Shen, Qilong
Bistrifluoromethylated organocuprate [Ph4P]+[Cu(CF3)2]−: synthesis, characterization and its application for trifluoromethylation of activated heteroaryl bromides, chlorides and iodides
Organic Chemistry Frontiers, 2019, 6, 2324
1554943 CIFC20 H22 N2 O4P 1 21/c 110.5905; 16.0282; 11.3851
90; 116.637; 90		1727.47Yakkala, Prasanna Anjaneyulu; Giri, Deepesh; Chaudhary, Bharatkumar; Auti, Prashant; Sharma, Satyasheel
Regioselective C‒H alkylation and alkenylation at the C5 position of 2-amino-1,4-naphthoquinones with maleimides under Rh(iii) catalysis
Organic Chemistry Frontiers, 2019, 6, 2441
1554945 CIFC17 H15 Br2 N O2P -17.5896; 10.9767; 11.9609
110.338; 100.049; 106.048		856.49Wang, Yu-Chao; Wang, Rui-Xiang; Qiu, Guanyinsheng; Zhou, Hongwei; Xie, Wenlin; Liu, Jin-Biao
ortho-Amide-directed 2,4-dibromohydration of conjugated enynes
Organic Chemistry Frontiers, 2019, 6, 2471
1554946 CIFC14 H12 N2 OP -17.2536; 9.2341; 9.3515
85.065; 81.059; 68.355		574.85Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines
Organic Chemistry Frontiers, 2019, 6, 2404
1554947 CIFC25 H15 N3 OP 1 21/n 19.8811; 14.4238; 13.7948
90; 109.258; 90		1856.1Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines
Organic Chemistry Frontiers, 2019, 6, 2404
1554949 CIFC25 H23 F2 N O3 SP -18.0332; 8.5272; 16.9075
99.329; 99.436; 101.204		1097.99Hu, Xiao-Si; Ding, Pei-Gang; Yu, Jin-Sheng; Zhou, Jian
A Sc(OTf)3 catalyzed Mukaiyama‒Mannich reaction of difluoroenoxysilanes with unactivated ketimines
Organic Chemistry Frontiers, 2019, 6, 2500
1554951 CIFC24 H24 O2 S2C 1 2 123.8323; 5.5909; 15.658
90; 103.617; 90		2027.7Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554952 CIFC25 H25 N O2 SP 21 21 216.07714; 13.1618; 27.1117
90; 90; 90		2168.56Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554953 CIFC32 H30.52 O4.26 SC 1 2/c 113.9336; 19.7182; 20.3209
90; 103.298; 90		5433.4Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554954 CIFC27 H24 Fe O2 SP b c a28.3482; 19.5347; 7.5873
90; 90; 90		4201.6Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554957 CIFC27 H22 Cl N O5 SP 21 21 2110.1603; 10.173; 23.5179
90; 90; 90		2430.83Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun
Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes
Organic Chemistry Frontiers, 2019, 6, 2452
1554958 CIFC27 H23 N O5 SP 1 21 110.0757; 10.4448; 10.8094
90; 92.786; 90		1136.2Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun
Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes
Organic Chemistry Frontiers, 2019, 6, 2452
1554961 CIFC30 H29 N O3 SP 1 21/n 19.8296; 13.4413; 22.608
90; 94.433; 90		2978.1Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554962 CIFC20 H27 N O2 SP 21 21 215.8832; 8.7875; 37.5443
90; 90; 90		1940.99Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554963 CIFC22 H29 N O2 SP 21 21 218.87; 10.6671; 21.508
90; 90; 90		2035Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554964 CIFC19 H23 N O2 SC 1 2/c 135.164; 8.6573; 11.5114
90; 94.241; 90		3494.8Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554965 CIFC23 H33 N O2 SP 1 21/c 119.505; 8.6857; 13.1687
90; 92.309; 90		2229.2Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506

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