Crystallography Open Database

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1553375 CIFC18 H26 O3P 21 21 2110.1815; 10.1849; 15.7912
90; 90; 90
1637.51Huang, Guang-Hui; Hu, Zhu; Lei, Chun; Wang, Pei-Pei; Yang, Jing; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Enantiomeric Pairs of Meroterpenoids with Diverse Heterocyclic Systems from Rhododendron nyingchiense.
Journal of natural products, 2018, 81, 1810-1818
1553382 CIFC16 H20 O7P 21 21 217.73476; 8.02415; 25.5244
90; 90; 90
1584.17Pang, Xiaoyan; Lin, Xiuping; Yang, Jie; Zhou, Xuefeng; Yang, Bin; Wang, Junfeng; Liu, Yonghong
Spiro-Phthalides and Isocoumarins Isolated from the Marine-Sponge-Derived Fungus Setosphaeria sp. SCSIO41009.
Journal of natural products, 2018, 81, 1860-1868
1553385 CIFC18 H26 O6P 21 21 216.7154; 15.1719; 17.1256
90; 90; 90
1744.8Xiong, Juan; Wang, Li-Jun; Qian, Jianchang; Wang, Pei-Pei; Wang, Xue-Jiao; Ma, Guang-Lei; Zeng, Huaqiang; Li, Jia; Hu, Jin-Feng
Structurally Diverse Sesquiterpenoids from the Endangered Ornamental Plant Michelia shiluensis.
Journal of natural products, 2018, 81, 2195-2204
1553388 CIFC19 H23 O6.5P 21 21 218.32583; 13.41861; 29.848
90; 90; 90
3334.65Huang, Hongbo; Song, Yongxiang; Li, Xin; Wang, Xin; Ling, Chunyao; Qin, Xiangjing; Zhou, Zhenbin; Li, Qinglian; Wei, Xiaoyi; Ju, Jianhua
Abyssomicin Monomers and Dimers from the Marine-Derived Streptomyces koyangensis SCSIO 5802.
Journal of natural products, 2018, 81, 1892-1898
1553389 CIFC19 H24 O7P 21 21 216.6414; 14.9068; 17.8924
90; 90; 90
1771.38Huang, Hongbo; Song, Yongxiang; Li, Xin; Wang, Xin; Ling, Chunyao; Qin, Xiangjing; Zhou, Zhenbin; Li, Qinglian; Wei, Xiaoyi; Ju, Jianhua
Abyssomicin Monomers and Dimers from the Marine-Derived Streptomyces koyangensis SCSIO 5802.
Journal of natural products, 2018, 81, 1892-1898
1553395 CIFC27 H46 O9P 21 21 216.9345; 13.2666; 28.7946
90; 90; 90
2649.02Sun, Na; Zhu, Yan; Zhou, Haofeng; Zhou, Junfei; Zhang, Hanqi; Zhang, Mengke; Zeng, Hong; Yao, Guangmin
Grayanane Diterpenoid Glucosides from the Leaves of Rhododendron micranthum and Their Bioactivities Evaluation.
Journal of natural products, 2018, 81, 2673-2681
1553397 CIFC30 H42 O4P 21 21 219.209; 14.6102; 18.3937
90; 90; 90
2474.79Tabefam, Marzieh; Moridi Farimani, Mahdi; Danton, Ombeline; Ramseyer, Justine; Nejad Ebrahimi, Samad; Neuburger, Markus; Kaiser, Marcel; Salehi, Peyman; Potterat, Olivier; Hamburger, Matthias
Antiprotozoal Isoprenoids from Salvia hydrangea.
Journal of natural products, 2018, 81, 2682-2691
1553402 CIFC21 H24 O8P 21 21 219.7873; 10.4684; 18.7272
90; 90; 90
1918.74Fragoso-Serrano, Mabel; Ortiz-Pastrana, Naytzé; Luna-Cruz, Norma; Toscano, Rubén A; Alpuche-Solís, Angel G; Ortega, Alfredo; Bautista, Elihú
Amarisolide F, an Acylated Diterpenoid Glucoside and Related Terpenoids from Salvia amarissima.
Journal of natural products, 2019, 82, 631-635
1553403 CIFC22 H22 O8P 21 21 216.9791; 12.6221; 22.9412
90; 90; 90
2020.91Fragoso-Serrano, Mabel; Ortiz-Pastrana, Naytzé; Luna-Cruz, Norma; Toscano, Rubén A; Alpuche-Solís, Angel G; Ortega, Alfredo; Bautista, Elihú
Amarisolide F, an Acylated Diterpenoid Glucoside and Related Terpenoids from Salvia amarissima.
Journal of natural products, 2019, 82, 631-635
1553419 CIFC28 H22 F3 N O5P 21 21 219.1158; 9.8126; 28.3116
90; 90; 90
2532.46Gao, Tai-Ping; Liu, Dan; Lin, Jun-Bing; Hu, Xiu-Qin; Wang, Zhu-Yin; Xu, Peng-Fei
Direct construction of chiral quaternary dihydropyranones through highly enantioselective organocatalytic hetero-Diels–Alder reactions of olefinic azlactones
Organic Chemistry Frontiers, 2016, 3, 598
1553421 CIFC20 H28 Cl N2 O4.5 SP 21 21 2111.701; 14.628; 25.939
90; 90; 90
4439.8Ye, Jian-Liang; Chen, Hang; Zhang, Yu-Feng; Huang, Pei-Qiang
A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline
Organic Chemistry Frontiers, 2016, 3, 683
1553430 CIFC17 H16 Cl N O2P 21 21 218.1449; 10.8999; 16.4545
90; 90; 90
1460.81Vyas, Vijyesh K.; Bhanage, Bhalchandra M.
Asymmetric transfer hydrogenation of seven membered tricyclic ketones: N-substituted dibenzo[b,e]azepine-6,11-dione driven by nonclassical CH/O interactions
Organic Chemistry Frontiers, 2016, 3, 614
1553444 CIFC16 H16 O3 SP 21 21 215.9262; 8.0475; 31.957
90; 90; 90
1524.06Phanindrudu, Mandalaparthi; Tiwari, Dipak Kumar; Sridhar, B.; Likhar, Pravin R.; Tiwari, Dharmendra Kumar
Magnetically separable nano-copper catalyzed unprecedented stereoselective synthesis of E-vinyl sulfones from tosylmethyl isocyanide and alkynes: TosMIC as a source of the sulfonyl group
Organic Chemistry Frontiers, 2016, 3, 795
1553449 CIFC32 H25 N O6P 21 21 219.02156; 9.44417; 30.948
90; 90; 90
2636.81Ran, Guang-Yao; Wang, Pan; Du, Wei; Chen, Ying-Chun
α-Regioselective [3 + 2] annulations with Morita‒Baylis‒Hillman carbonates of isatins and 2-nitro-1,3-enynes
Organic Chemistry Frontiers, 2016, 3, 861
1553467 CIFC14 H10 Br N O2P 21 21 214.4197; 11.6677; 22.915
90; 90; 90
1181.7Zhang, Xu; Xu, Bin; Xu, Ming-Hua
Rhodium-catalyzed asymmetric arylation of N- and O-containing cyclic aldimines: facile and efficient access to highly optically active 3,4-dihydrobenzo[1,4]oxazin-2-ones and dihydroquinoxalinones
Organic Chemistry Frontiers, 2016, 3, 944
1553487 CIFC21 H19 Br N2 O4P 21 21 218.4058; 10.8659; 21.9188
90; 90; 90
2001.99Ma, Qiao; Gong, Lei; Meggers, Eric
Enantioselective β-alkylation of pyrroles with the formation of an all-carbon quaternary stereocenter
Organic Chemistry Frontiers, 2016, 3, 1319
1553492 CIFC29 H44 O6 SiP 21 21 2111.5223; 14.9948; 16.4141
90; 90; 90
2835.9Pérez-Estrada, S.; Sayar, N.; Granja, J. R.
Towards taxane analogues synthesis by dienyne ring closing metathesis
Organic Chemistry Frontiers, 2016, 3, 1331
1553498 CIFC14 H17 N5 O4P 21 21 217.51038; 17.3551; 23.2172
90; 90; 90
3026.21Naik, Siddhi D.; Chandra, Girish; Sahu, Pramod K.; Kim, Hong-Rae; Qu, Shuhao; Yoon, Ji-seong; Jeong, Lak Shin
Stereo- and regio-selective synthesis of 3′-C-substituted-(N)-methanocarba adenosines as potential anticancer agents
Organic Chemistry Frontiers, 2016, 3, 1472
1553501 CIFC24 H15 NP 21 21 214.8217; 10.1093; 31.14
90; 90; 90
1517.89Zagranyarski, Yulian; Skabeev, Artem; Ma, Yingjie; Müllen, Klaus; Li, Chen
Facile synthesis of annulated heterocyclic benzo[kl]acridine derivatives via one-pot N–H/C–H coupling
Organic Chemistry Frontiers, 2016, 3, 1520
1553506 CIFC31 H27 N2 O2P 21 21 218.681; 17.323; 32.77
90; 90; 90
4928Chen, Zhen; Huo, Yuwen; An, Ping; Wang, Xichao; Song, Chun; Ma, Yudao
[2.2]Paracyclophane-based N-heterocyclic carbene as efficient catalyst or as ligand for copper catalyst for asymmetric α-silylation of N-tosylaldimines
Organic Chemistry Frontiers, 2016, 3, 1725
1553508 CIFC17 H31 N O4P 21 21 216.03; 16.334; 18.224
90; 90; 90
1795Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553510 CIFC13 H21 N O3P 21 21 216.078; 10.204; 19.957
90; 90; 90
1237.73Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553519 CIFC36 H32 F2 N2 O2P 21 21 2111.5593; 14.0068; 17.8914
90; 90; 90
2896.78Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng
Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles
Organic Chemistry Frontiers, 2017, 4, 57
1553531 CIFC30 H50 O3P 21 21 216.52391; 12.9427; 31.7963
90; 90; 90
2684.78Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing
A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum
Organic Chemistry Frontiers, 2017, 4, 42
1553558 CIFC20 H14 OP 21 21 217.9447; 10.3826; 17.0108
90; 90; 90
1403.16Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G.
Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans
Organic Chemistry Frontiers, 2017, 4, 972
1553569 CIFC31 H27 Br N4 O3P 21 21 219.662; 12.286; 24.441
90; 90; 90
2901Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang
Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst
Organic Chemistry Frontiers, 2017, 4, 101
1553571 CIFC15 H17 Cl N2 O3P 21 21 217.2915; 12.7983; 15.9552
90; 90; 90
1488.92Peng, Xiao-Jiao; Ho, Yee Ann; Wang, Zhi-Peng; Shao, Pan-Lin; Zhao, Yu; He, Yun
Formal [3 + 2] cycloaddition of α-unsubstituted isocyanoacetates and methyleneindolinones: enantioselective synthesis of spirooxindoles
Organic Chemistry Frontiers, 2017, 4, 81
1553572 CIFC15 H11 Cl F3 N3 O3P 21 21 217.74798; 9.1129; 21.719
90; 90; 90
1533.5Hao, Xin-Qi; Wang, Cong; Liu, Shuang-Liang; Wang, Xiao; Wang, Li; Gong, Jun-Fang; Song, Mao-Ping
Cobalt(ii)/(imidazoline–oxazoline)-catalyzed enantioselective Michael addition of 2-acetyl azaarenes to β-CF3-β-disubstituted nitroalkenes
Organic Chemistry Frontiers, 2017, 4, 308
1553578 CIFC11 H14 Br F O2P 21 21 215.651; 16.364; 38.4918
90; 90; 90
3559Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian
Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities
Organic Chemistry Frontiers, 2017, 4, 1084
1553603 CIFC71 H46 B F24 Ir N O PP 21 21 2112.2302; 15.3106; 36.571
90; 90; 90
6848Wang, Qian; Zhang, Zongpeng; Chen, Caiyou; Yang, Hailong; Han, Zhengyu; Dong, Xiu-Qin; Zhang, Xumu
Iridium catalysts with modular axial-unfixed biphenyl phosphine‒oxazoline ligands: asymmetric hydrogenation of α,β-unsaturated carboxylic acids
Organic Chemistry Frontiers, 2017, 4, 627
1553611 CIFC31 H23 Cl0 N O4P 21 21 219.9046; 10.4946; 23.736
90; 90; 90
2467.2Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding
Organocatalytic C‒C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins
Organic Chemistry Frontiers, 2017, 4, 560
1553615 CIFC23 H19 N O2 S2P 21 21 218.189; 14.782; 17.421
90; 90; 90
2108.8Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming
A copper-catalyzed arylation/nucleophilic addition/fragmentation/C–S bond formation cascade: synthesis of bis(arylthio)imines
Organic Chemistry Frontiers, 2017, 4, 510
1553629 CIFC51 H29 Cl3 O4P 21 21 2110.5417; 14.8356; 24.1274
90; 90; 90
3773.3Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553632 CIFC20 H19 Br N2 O5 SP 21 21 218.8208; 12.857; 18.1141
90; 90; 90
2054.3Yu, Lu; Cheng, Yuyu; Qi, Fei; Li, Rou; Li, Pengfei
Organocatalytic regioselective, diastereoselective, and enantioselective annulation of cyclic 1-azadienes with γ-nitro ketones via 3,4-cyclization
Organic Chemistry Frontiers, 2017, 4, 1336
1553636 CIFC25 H20 N2 O2 SP 21 21 217.7445; 13.971; 19.15
90; 90; 90
2072Lin, Ye; Liu, Lei; Du, Da-Ming
Squaramide-catalyzed asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles with chalcones for synthesis of pyrrolidinyl spirooxindoles
Organic Chemistry Frontiers, 2017, 4, 1229
1553637 CIFC16 H21 N3 O5P 21 21 218.4855; 15.887; 25.5299
90; 90; 90
3441.7Deng, Tao; Thota, Ganesh Kumar; Li, Yi; Kang, Qiang
Enantioselective conjugate addition of hydroxylamines to α,β-unsaturated 2-acyl imidazoles catalyzed by a chiral-at-metal Rh(iii) complex
Organic Chemistry Frontiers, 2017, 4, 573
1553670 CIFC30 H34 N4 O6P 21 21 216.29545; 15.9502; 28.8235
90; 90; 90
2894.27Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng
Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties
Materials Chemistry Frontiers, 2017, 1, 1041
1553682 CIFC17 H16 I N O2P 21 21 216.1493; 12.443; 19.762
90; 90; 90
1512.1Butler, Tristan; Wang, Fang; Sabat, Michal; Fraser, Cassandra L.
Controlling solid-state optical properties of stimuli responsive dimethylamino-substituted dibenzoylmethane materials
Materials Chemistry Frontiers, 2017, 1, 1804
1553726 CIFC16 H15 N O7P 21 21 2111.4884; 11.9792; 20.8251
90; 90; 90
2866Wang, Junliang; Li, Jianneng; Shen, Xianwang; Dong, Cong; Lin, Jun; Wei, Kun
Asymmetric total synthesis of (−)-δ-lycorane
Organic Chemistry Frontiers, 2017, 4, 1149
1553729 CIFC19 H10 F4 O2 SP 21 21 216.6977; 8.1914; 30.513
90; 90; 90
1674.1Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553730 CIFC15 H15 F3 O5 SP 21 21 217.5426; 13.2312; 15.9887
90; 90; 90
1595.6Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553731 CIFC17 H11 F3 N2 O SP 21 21 218.5502; 11.0835; 16.8212
90; 90; 90
1594.1Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553755 CIFC7.75 H7.75 F7.75 N7.75 O7.75 S7.75P 21 21 218.086; 14.196; 23.304
90; 90; 90
2675Pouambeka, Tony Wheellyam; Zhang, Ge; Zheng, Guang-Fan; Xu, Guo-Xing; Zhang, Qian; Xiong, Tao; Zhang, Qian
Copper-catalyzed oxidative amidation of α,β-unsaturated ketones via selective C‒H or C‒C bond cleavage
Organic Chemistry Frontiers, 2017, 4, 1420
1553756 CIFC27 H21 N O2 S2P 21 21 215.9608; 18.7773; 20.3817
90; 90; 90
2281.3Shi, Qing; Li, Pinhua; Zhang, Yan; Wang, Lei
Visible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions
Organic Chemistry Frontiers, 2017, 4, 1322
1553758 CIFC17 H18 Br F3 N2 O6P 21 21 218.3955; 14.09; 16.7651
90; 90; 90
1983.19Liu, Qiang; Zhao, Kun; Zhi, Ying; Raabe, Gerhard; Enders, Dieter
Squaramide-catalyzed domino Michael/aza-Henry [3 + 2] cycloaddition: asymmetric synthesis of functionalized 5-trifluoromethyl and 3-nitro substituted pyrrolidines
Organic Chemistry Frontiers, 2017, 4, 1416
1553761 CIFC17 H16 OP 21 21 217.738; 11.656; 14.0895
90; 90; 90
1270.79Zhang, Bo-Sheng; Hua, Hui-Liang; Gao, Lu-Yao; Liu, Ce; Qiu, Yi-Feng; Zhou, Ping-Xin; Zhou, Zhao-Zhao; Zhao, Jia-Hui; Liang, Yong-Min
Palladium-catalyzed arene C–H activation/ketone C–H functionalization reaction: route to spirodihydroindenones
Organic Chemistry Frontiers, 2017, 4, 1376
1553777 CIFC10 H12 O2 SP 21 21 215.7817; 8.2558; 19.972
90; 90; 90
953.3Meng, Ke; Xia, Jingzhao; Wang, Yanzhao; Zhang, Xinghua; Yang, Guoqiang; Zhang, Wanbin
Ir/BiphPHOX-catalyzed asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles and 2,5-dihydrothiophene 1,1-dioxides
Organic Chemistry Frontiers, 2017, 4, 1601
1553786 CIFC27 H23 Cl F3 N O3P 21 21 218.5817; 10.4128; 27.6259
90; 90; 90
2468.64Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang
Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2017, 4, 1772
1553787 CIFC15 H16 F3 N O2 SP 21 21 216.2282; 7.0351; 36.2461
90; 90; 90
1588.16Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang
Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2017, 4, 1772
1553792 CIFC33 H27 O2 PP 21 21 219.0757; 10.4623; 26.2445
90; 90; 90
2491.99Li, Bin; Zhang, Mingkai; Huang, Xulun; Gu, Zhenhua
Synthesis of 2,3-dihydro-1H-phosphindole-1-oxides via the t-BuLi-mediated rearrangement of vinyl bromides and phosphine oxides
Organic Chemistry Frontiers, 2017, 4, 1854
1553806 CIFC22 H19 N O5 SP 21 21 218.8173; 14.3926; 15.3659
90; 90; 90
1949.99Xie, Lei; Ma, Hongli; Li, Jiaqi; Yu, Yuan; Qin, Zhaohai; Fu, Bin
Ni(ii)-Catalyzed enantioselective Mukaiyama–Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters
Organic Chemistry Frontiers, 2017, 4, 1858
1553815 CIFC23 H23 Cl O7P 21 21 216.82668; 9.4989; 34.5079
90; 90; 90
2237.7Yao, Qian; Lin, Lili; Zhang, Hang; Yu, Han; Xiong, Qian; Liu, Xiaohua; Feng, Xiaoming
The asymmetric synthesis of multisubstituted diquinanes via the domino reaction of electron-deficient enynes
Organic Chemistry Frontiers, 2017, 4, 2012
1553838 CIFC29 H25 N O7 SP 21 21 218.0159; 15.545; 21.174
90; 90; 90
2638.4Li, Shoulei; Zhang, Enge; Feng, Junjun; Li, Xin
An enantioselective conjugate addition reaction of 3-substituted benzothiophen-2-ones and 2-phthalimidoacrylates
Organic Chemistry Frontiers, 2017, 4, 2301
1553843 CIFC16 H15 N O4P 21 21 217.973; 12.9128; 14.3781
90; 90; 90
1480.28Wu, Qiuju; Li, Chengcheng; Wang, Weihong; Wang, Hongling; Pan, Dingwu; Zheng, Pengcheng
NHC-catalyzed enantioselective synthesis of dihydropyran-4-carbonitriles bearing all-carbon quaternary centers
Organic Chemistry Frontiers, 2017, 4, 2323
1553850 CIFC18 H16 O4 SP 21 21 219.7797; 10.9021; 14.8619
90; 90; 90
1584.6Zhao, Wei-Wei; Liu, Yan-Kai
Enantio- and diastereoselective synthesis of tetrahydrofuro[2,3-b]furan-2(3H)-one derivatives and related oxygen heterocycles via an asymmetric organocatalytic cascade process
Organic Chemistry Frontiers, 2017, 4, 2358
1553855 CIFC18 H16 Cl N O4 SP 21 21 215.1621; 16.3247; 20.251
90; 90; 90
1706.5Deng, Hua; He, Fu-Sheng; Li, Cong-Shan; Yang, Wu-Lin; Deng, Wei-Ping
Enantioselective construction of tricyclic pyrrolidine-fused benzo[b]thiophene 1,1-dioxide derivatives via copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition
Organic Chemistry Frontiers, 2017, 4, 2343
1553871 CIFC31 H38 O9P 21 21 2114.6815; 17.2043; 23.1115
90; 90; 90
5837.62Luo, Jun; Huang, Wan-Sha; Hu, Sheng-Mou; Zhang, Pan-Pan; Zhou, Xu-Wei; Wang, Xiao-Bing; Yang, Ming-Hua; Luo, Jian-Guang; Wang, Chen; Liu, Chang; Yao, He-Quan; Zhang, Can; Sun, Hong-Bin; Chen, Yi-Jun; Kong, Ling-Yi
Rearranged limonoids with unique 6/5/6/5 tetracarbocyclic skeletons from Toona ciliata and biomimetic structure divergence
Organic Chemistry Frontiers, 2017, 4, 2417
1553872 CIFC30 H30 I N3 O5P 21 21 2112.1518; 12.3848; 19.412
90; 90; 90
2921.5Zhu, Jing-Yan; Yang, Wu-Lin; Liu, Yang-Zi; Shang, Shao-Jing; Deng, Wei-Ping
A copper(i)-catalyzed asymmetric Mannich reaction of glycine Schiff bases with isatin-derived ketimines: enantioselective synthesis of 3-substituted 3-aminooxindoles
Organic Chemistry Frontiers, 2018, 5, 70
1553873 CIFC13 H23 N O4 SP 21 21 216.1598; 8.133; 31.1006
90; 90; 90
1558.07Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun
Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters
Organic Chemistry Frontiers, 2018, 5, 36
1553874 CIFC21 H24 N2 O6 SP 21 21 217.9925; 13.9906; 19.0487
90; 90; 90
2130.02Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun
Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters
Organic Chemistry Frontiers, 2018, 5, 36
1553899 CIFC14 H19 N O3 SP 21 21 215.36821; 11.71337; 21.6232
90; 90; 90
1359.66Reboredo, Silvia; García-Marijuan, Ainara; Uria, Uxue; Reyes, Efraím; Carrillo, Luisa; Ugarriza, Iratxe; Vicario, Jose L.
Highly diastereoselective C → N acyl rearrangement in polysubstituted pyrrolidine 2,2-dicarboxylates. Stereocontrolled synthesis of densely functionalized prolines
Organic Chemistry Frontiers, 2018, 5, 933
1553901 CIFC17 H17 N O3P 21 21 216.5337; 8.4509; 26.0879
90; 90; 90
1440.46Xu, Youguo; Zhang, Sheng; Li, Lijun; Wang, Yukang; Zha, Zhenggen; Wang, Zhiyong
l-Phenylalanine potassium catalyzed asymmetric formal [3 + 3] annulation of 2-enoyl-pyridine N-oxides with acetone
Organic Chemistry Frontiers, 2018, 5, 376
1553936 CIFC26 H28 Cl2 N3 O5 P RuP 21 21 218.4287; 10.7538; 30.9419
90; 90; 90
2804.59de Julián, E.; Menéndez-Pedregal, E.; Claros, M.; Vaquero, M.; Díez, J.; Lastra, E.; Gamasa, P.; Pizzano, A.
Practical synthesis of enantiopure benzylamines by catalytic hydrogenation or transfer hydrogenation reactions in isopropanol using a Ru-pybox catalyst
Organic Chemistry Frontiers, 2018, 5, 841
1553949 CIFC19 H17 F3 N O3.5P 21 21 218.0275; 13.876; 31.686
90; 90; 90
3529.5Huang, Bing-Bing; Wu, Liang; Liu, Ren-Rong; Xing, Ling-Ling; Liang, Ren-Xiao; Jia, Yi-Xia
Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters
Organic Chemistry Frontiers, 2018, 5, 929
1553963 CIFC23 H21 N O2 SP 21 21 218.0484; 10.6055; 21.9053
90; 90; 90
1869.8Li, Yun; Chen, Jingchao; He, Zhenxiu; Qin, Hongyu; Zhou, Yongyun; Khan, Ruhima; Fan, Baomin
Cobalt-catalyzed asymmetric reactions of heterobicyclic alkenes with in situ generated organozinc halides
Organic Chemistry Frontiers, 2018, 5, 1108
1553966 CIFC18 H21 N O2 SP 21 21 219.4077; 9.9254; 17.562
90; 90; 90
1639.9Song, Bo; Chen, Mu-Wang; Zhou, Yong-Gui
Synthesis of chiral sultams with two adjacent stereocenters via palladium-catalyzed dynamic kinetic resolution
Organic Chemistry Frontiers, 2018, 5, 1113
1553974 CIFC24 H25 Cl2 N OP 21 21 218.799; 14.7395; 16.0279
90; 90; 90
2078.7Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie
Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives
Organic Chemistry Frontiers, 2018, 5, 1366
1553975 CIFC22 H23 N O SP 21 21 215.6782; 8.5568; 38.5091
90; 90; 90
1871.05Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie
Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives
Organic Chemistry Frontiers, 2018, 5, 1366
1553977 CIFC34 H28 N O6 P SP 21 21 2111.9446; 13.7058; 19.238
90; 90; 90
3149.5Gu, Zheng; Zhou, Ji; Jiang, Guo-Fang; Zhou, Yong-Gui
Synthesis of chiral γ-aminophosphonates through the organocatalytic hydrophosphonylation of azadienes with phosphites
Organic Chemistry Frontiers, 2018, 5, 1148
1553978 CIFC18 H18 O2P 21 21 217.9384; 9.9744; 17.126
90; 90; 90
1356Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy
Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems
Organic Chemistry Frontiers, 2018, 5, 1320
1554009 CIFC9 H8 O3P 21 21 215.8715; 9.4021; 13.3312
90; 90; 90
735.94Gianopoulos, Christopher G.; Zarychta, Bartosz; Cenedese, Simone; Zhurov, Vladimir V.; Pinkerton, A. Alan
Experimental and Theoretical Electron Density Determination for Two Norbornene Derivatives: Topological Analysis Provides Insights on Reactivity.
The journal of physical chemistry. A, 2016, 120, 4059-4070
1554010 CIFC8 H6 O4P 21 21 215.3018; 6.9265; 18.6795
90; 90; 90
685.97Gianopoulos, Christopher G.; Zarychta, Bartosz; Cenedese, Simone; Zhurov, Vladimir V.; Pinkerton, A. Alan
Experimental and Theoretical Electron Density Determination for Two Norbornene Derivatives: Topological Analysis Provides Insights on Reactivity.
The journal of physical chemistry. A, 2016, 120, 4059-4070
1554034 CIFC6 Br2 N4 O4 SP 21 21 216.57487; 10.21418; 15.22634
90; 90; 90
1022.55Pavan, Mysore S.; Jana, Ajay Kumar; Natarajan, S.; Guru Row, Tayur N.
Halogen Bonding and Chalcogen Bonding in 4,7-Dibromo-5,6-dinitro-2,1,3-benzothiadiazole.
The journal of physical chemistry. B, 2015, 119, 11382-11390
1554051 CIFC4 H8 B F4 Li O2 SP 21 21 215.156; 8.8536; 18.337
90; 90; 90
837.1Dokko, Kaoru; Watanabe, Daiki; Ugata, Yosuke; Thomas, Morgan L.; Tsuzuki, Seiji; Shinoda, Wataru; Hashimoto, Kei; Ueno, Kazuhide; Umebayashi, Yasuhiro; Watanabe, Masayoshi
Direct Evidence for Li Ion Hopping Conduction in Highly Concentrated Sulfolane-Based Liquid Electrolytes.
The journal of physical chemistry. B, 2018, 122, 10736-10745
1554069 CIFC6 H16 N2 O3P 21 21 215.93493; 6.94133; 20.5754
90; 90; 90
847.63Williams, P. Andrew; Hughes, Colan E.; Martin, Jean; Courvoisier, Emilie; Buanz, Asma B. M.; Gaisford, Simon; Harris, Kenneth D. M.
Understanding the Solid-State Hydration Behavior of a Common Amino Acid: Identification, Structural Characterization, and Hydration/Dehydration Processes of New Hydrate Phases of l-Lysine
The Journal of Physical Chemistry C, 2016, 120, 9385
1554087 CIFC14 H14 N4 SP 21 21 216.0478; 12.876; 16.732
90; 90; 90
1302.9Price, Jacquelyn T.; Li, Michelle S. M.; Brazeau, Allison L.; Tao, Danlei; Xiang, Guiming; Chen, Yanhua; McDonald, Robert; Jones, Nathan D.; Ding, Zhifeng
Structural Insight into Electrogenerated Chemiluminescence of Para-Substituted Aryl–Triazole–Thienyl Compounds
The Journal of Physical Chemistry C, 2016, 120, 21778
1554093 CIFC26 H24 N2 O4P 21 21 219.65062; 11.62065; 19.4417
90; 90; 90
2180.32Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin
Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers
The Journal of Physical Chemistry C, 2017, 121, 25503
1554094 CIFC26 H24 N2 O4P 21 21 219.754; 11.691; 19.628
90; 90; 90
2238.3Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin
Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers
The Journal of Physical Chemistry C, 2017, 121, 25503
1554120 CIFC43 H36 N2 O2 SP 21 21 2112.9552; 12.9939; 20.0294
90; 90; 90
3371.72Kukhta, Nadzeya A.; Batsanov, Andrei S.; Bryce, Martin R.; Monkman, Andrew P.
Importance of Chromophore Rigidity on the Efficiency of Blue Thermally Activated Delayed Fluorescence Emitters
The Journal of Physical Chemistry C, 2018, 122, 28564
1554138 CIFC6 H8 F6 Li N O6 S3P 21 21 218.6999; 12.2951; 14.5055
90; 90; 90
1551.6Nakanishi, Azusa; Ueno, Kazuhide; Watanabe, Daiki; Ugata, Yosuke; Matsumae, Yoshiharu; Liu, Jiali; Thomas, Morgan L.; Dokko, Kaoru; Watanabe, Masayoshi
Sulfolane-Based Highly Concentrated Electrolytes of Lithium Bis(trifluoromethanesulfonyl)amide: Ionic Transport, Li-Ion Coordination, and Li‒S Battery Performance
The Journal of Physical Chemistry C, 2019, 123, 14229
1554214 CIFC34 H16 N4P 21 21 217.1719; 10.8284; 29.7864
90; 90; 90
2313.2Yoshida, Yukihiro; Tango, Shunsuke; Isomura, Kazuhide; Nakamura, Yuto; Kishida, Hideo; Koretsune, Takashi; Sakata, Masafumi; Nakano, Yoshiaki; Yamochi, Hideki; Saito, Gunzi
Charge-transfer complexes based on C2v-symmetric benzo[ghi]perylene: comparison of their dynamic and electronic properties with those of D6h-symmetric coronene
Materials Chemistry Frontiers, 2018, 2, 1165
1554229 CIFC26 H16 I4P 21 21 219.8155; 15.6764; 22.6588
90; 90; 90
3486.55Xiong, Jianbo; Li, Xinyue; Yuan, Chunqing; Semin, Sergey; Yao, Zhaoquan; Xu, Jialiang; Rasing, Theo; Bu, Xian-He
Wavelength dependent nonlinear optical response of tetraphenylethene aggregation-induced emission luminogens
Materials Chemistry Frontiers, 2018, 2, 2263
1554230 CIFC26 H16 Br4P 21 21 219.6034; 15.4711; 22.0743
90; 90; 90
3279.69Xiong, Jianbo; Li, Xinyue; Yuan, Chunqing; Semin, Sergey; Yao, Zhaoquan; Xu, Jialiang; Rasing, Theo; Bu, Xian-He
Wavelength dependent nonlinear optical response of tetraphenylethene aggregation-induced emission luminogens
Materials Chemistry Frontiers, 2018, 2, 2263
1554237 CIFC25 H20 SP 21 21 215.988; 7.36; 45.02
90; 90; 90
1984.1Wang, Can; Yu, Yun; Chai, Zhaofei; He, Fangdi; Wu, Chaozheng; Gong, Yanbin; Han, Mengmeng; Li, Qianqian; Li, Zhen
Recyclable mechanoluminescent luminogen: different polymorphs, different self-assembly effects of the thiophene moiety and recovered molecular packing via simple thermal-treatment
Materials Chemistry Frontiers, 2019, 3, 32
1554253 CIFC25 H21 Br F3 N3 O4 SP 21 21 218.8119; 10.4134; 27.1396
90; 90; 90
2490.38Zhu, Wen-Run; Chen, Qing; Lin, Ning; Chen, Kai-Bin; Zhang, Zhen-Wei; Fang, Gang; Weng, Jiang; Lu, Gui
Organocatalytic Michael/cyclization cascade reactions of 3-isothiocyanato oxindoles with 3-trifluoroethylidene oxindoles: an approach for the synthesis of 3′-trifluoromethyl substituted 3,2′-pyrrolidinyl-bispirooxindoles
Organic Chemistry Frontiers, 2018, 5, 1375
1554255 CIFC28 H38 O9P 21 21 218.3949; 15.0525; 22.267
90; 90; 90
2813.8Yin, Guo-Ping; Wu, Ya-Rong; Han, Chao; Wang, Xiao-Bing; Gao, Hong-Liang; Yin, Yong; Kong, Ling-Yi; Yang, Ming-Hua
Asperones A–E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1–15
Organic Chemistry Frontiers, 2018, 5, 2432
1554256 CIFC37 H42 O11P 21 21 219.34542; 14.58845; 24.65138
90; 90; 90
3360.85Xu, Jianlin; Tan, Haibo; Chen, Yuchan; Li, Saini; Huang, Zilei; Guo, Heng; Li, Haohua; Gao, Xiaoxia; Liu, Hongxin; Zhang, Weimin
Lithocarpins A–D: four tenellone-macrolide conjugated [4 + 2] hetero-adducts from the deep-sea derived fungus Phomopsis lithocarpus FS508
Organic Chemistry Frontiers, 2018, 5, 1792
1554271 CIFC35 H44 O12P 21 21 219.18292; 12.4621; 28.4369
90; 90; 90
3254.28Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554272 CIFC74 H90 Cl12 O24P 21 21 2115.8696; 16.1185; 32.0556
90; 90; 90
8199.6Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554274 CIFC74 H91 N2 O24P 21 21 2115.2487; 16.1229; 29.1352
90; 90; 90
7163Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554298 CIFC26 H39 Cl2 Co N3 O12P 21 21 2110.4066; 26.417; 12.0692
90; 90; 90
3318Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554299 CIFC26 H39 Cl2 N3 Ni O12P 21 21 2110.3907; 11.9429; 26.537
90; 90; 90
3293.1Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554301 CIFC26 H41 Cl2 Fe N3 O12P 21 21 2110.3081; 11.98; 26.1548
90; 90; 90
3229.88Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554316 CIFC32 H31 N O5P 21 21 2110.1535; 10.5316; 25.565
90; 90; 90
2733.73Duan, Chuan-Qi; He, Xiao-Long; Du, Wei; Chen, Ying-Chun
Asymmetric [4 + 2] cycloadditions with 3-furfural derivatives and α-cyano-α,β-unsaturated ketones
Organic Chemistry Frontiers, 2018, 5, 2057
1554320 CIFC38 H28 N2 O3 SP 21 21 219.00774; 11.44511; 29.0288
90; 90; 90
2992.71Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming
Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives
Organic Chemistry Frontiers, 2018, 5, 2126
1554334 CIFC34 H34 Cl3 Fe N3 O4P 21 21 219.5467; 13.5703; 26.06
90; 90; 90
3376.1Zhang, Yuehua; Wang, Chunting; Huang, Wei; Haruehanroengra, Phensinee; Peng, Cheng; Sheng, Jia; Han, Bo; He, Gu
Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone–ferrocene hybrids as novel RalA inhibitors
Organic Chemistry Frontiers, 2018, 5, 2229
1554340 CIFC20 H24 Cl N O3P 21 21 217.508; 11.2397; 21.9828
90; 90; 90
1855.08Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.
Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines
Organic Chemistry Frontiers, 2018, 5, 2171
1554355 CIFC20 H32 O5P 21 21 216.6084; 11.8396; 22.9114
90; 90; 90
1792.61Hu, Zheng-Xi; Xu, Hou-Chao; Hu, Kun; Liu, Miao; Li, Xiao-Nian; Li, Xing-Ren; Du, Xue; Zhang, Yong-Hui; Puno, Pema-Tenzin; Sun, Han-Dong
Structurally diverse diterpenoids from Isodon pharicus
Organic Chemistry Frontiers, 2018, 5, 2379
1554380 CIFC29 H28 Cl N3 O7P 21 21 218.611; 11.3415; 28.819
90; 90; 90
2814.5Wei, Qinghua; Ma, Xiaochu; Chen, Jianghui; Niu, Li; Yang, Xi; Xia, Fei; Liu, Shunying
A triple-functionalised metal centre-catalyzed enantioselective multicomponent reaction
Organic Chemistry Frontiers, 2018, 5, 2799
1554423 CIFC17 H0.25 N OP 21 21 216.229; 13.6065; 14.6177
90; 90; 90
1238.92Xu, Xin-Ming; Lei, Chuan-Hu; Tong, Shuo; Zhu, Jieping; Wang, Mei-Xiang
Lewis acid catalyst-steered divergent synthesis of functionalized vicinal amino alcohols and pyrroles from tertiary enamides
Organic Chemistry Frontiers, 2018, 5, 3138
1554436 CIFC21 H21 Br N O7 P SP 21 21 218.8385; 14.3341; 17.8495
90; 90; 90
2261.4Sun, Jun; Mou, Chengli; Liu, Changyi; Huang, Ruoyan; Zhang, Shupeng; Zheng, Pengcheng; Chi, Yonggui Robin
Enantioselective access to multi-cyclic α-amino phosphonates via carbene-catalyzed cycloaddition reactions between enals and six-membered cyclic imines
Organic Chemistry Frontiers, 2018, 5, 2992
1554456 CIFC6 H7 O5 PP 21 21 214.6005; 10.122; 16.4334
90; 90; 90
765.24Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.
Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes
Organic Chemistry Frontiers, 2018, 5, 3113
1554484 CIFC11 H9 F O2P 21 21 214.9693; 5.8579; 31.3863
90; 90; 90
913.64Han, Sang Hoon; Pandey, Ashok Kumar; Lee, Heeyoung; Kim, Saegun; Kang, Dahye; Jung, Young Hoon; Kim, Hyung Sik; Hong, Sungwoo; Kim, In Su
One-pot synthesis of 2-naphthols from nitrones and MBH adducts via decarboxylative N–O bond cleavage
Organic Chemistry Frontiers, 2018, 5, 3210
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
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
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
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
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
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
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
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 CIFC31 H42 O11P 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
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
1554593 CIFC15 H13 O6.5P 21 21 217.4082; 7.9771; 43.956
90; 90; 90
2597.6Szwalbe, Agnieszka J.; Williams, Katherine; Song, Zhongshu; de Mattos-Shipley, Kate; Vincent, Jason L.; Bailey, Andrew M.; Willis, Christine L.; Cox, Russell J.; Simpson, Thomas J.
Characterisation of the biosynthetic pathway to agnestins A and B reveals the reductive route to chrysophanol in fungi.
Chemical science, 2019, 10, 233-238
1554602 CIFC77 H77 N15 O2 Rb UP 21 21 2113.6821; 21.8875; 24.244
90; 90; 90
7260.28Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554603 CIFC62 H62 I N12 O2 U ZnP 21 21 2113.273; 16.4368; 27.8646
90; 90; 90
6079.1Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554637 CIFC43 H38 Cl2 N4 O2 Pt2P 21 21 2111.0565; 16.7748; 20.3659
90; 90; 90
3777.3Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554639 CIFC51 H35 Cl3 N4 O2 Pt2P 21 21 2110.7354; 20.1891; 21.7815
90; 90; 90
4720.9Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554640 CIFC43 H38 Cl2 N4 O2 Pt2P 21 21 2111.05822; 16.7782; 20.3868
90; 90; 90
3782.51Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554680 CIFC27 H18 N4 O PtP 21 21 217.7277; 13.36; 20.072
90; 90; 90
2072.3Ma, Huili; Shen, Kang; Wu, Yipei; Xia, Fang; Yu, Feiling; Sun, Zhengyi; Qian, Chunyue; Peng, Qiming; Zhang, Hong-Hai; You, Cong; Xie, Guohua; Hang, Xiao-Chun; Huang, Wei
High-color-purity and efficient solution-processable blue phosphorescent light-emitting diodes with Pt(ii) complexes featuring 3ππ* transitions
Materials Chemistry Frontiers, 2019, 3, 2448
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
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
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
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
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
1554753 CIFC31 H26 Cl N O4P 21 21 217.9152; 11.4088; 28.388
90; 90; 90
2563.5He, Zhao-Lin; Sheong, Fu Kit; Li, Qing-Hua; Lin, Zhenyang; Wang, Chun-Jiang
Exoselective 1,3-dipolar [3 + 6] cycloaddition of azomethine ylides with 2-acylcycloheptatrienes: stereoselectivity and mechanistic insight.
Organic letters, 2015, 17, 1365-1368
1554776 CIFC35 H26 N1.6 O10P 21 21 2113.871; 15.1622; 64.627
90; 90; 90
13592Cao, Pei; Yang, Jing; Miao, Cui-Ping; Yan, Yijun; Ma, Ya-Tuan; Li, Xiao-Nian; Zhao, Li-Xing; Huang, Sheng-Xiong
New duclauxamide from Penicillium manginii YIM PH30375 and structure revision of the duclauxin family.
Organic letters, 2015, 17, 1146-1149
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
1554793 CIFC24 H21 I N2 O3 SP 21 21 2110.7482; 12.7229; 16.152
90; 90; 90
2208.76Fu, Shaomin; Yang, Honghao; Li, Guoqiang; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Copper(II)-catalyzed enantioselective intramolecular cyclization of N-alkenylureas.
Organic letters, 2015, 17, 1018-1021
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
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
1554804 CIFC40 H43 B2 Fe PP 21 21 2110.3874; 17.4963; 18.3521
90; 90; 90
3335.3Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
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
1554814 CIFC34 H35 N O6 SP 21 21 219.4387; 22.551; 28.131
90; 90; 90
5987.7Peng, Peng; Geng, Yiqun; Göttker-Schnetmann, Inigo; Schmidt, Richard R.
2-Nitro-thioglycosides: α- and β-selective generation and their potential as β-selective glycosyl donors.
Organic letters, 2015, 17, 1421-1424
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
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
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
1554841 CIFC14 H15 Br N2 O2P 21 21 219.2455; 10.1411; 14.412
90; 90; 90
1351.3Gu, Xiaodong; Dai, Yuanyuan; Guo, Tingting; Franchino, Allegra; Dixon, Darren J.; Ye, Jinxing
A general, scalable, organocatalytic nitro-Michael addition to enones: enantioselective access to all-carbon quaternary stereocenters.
Organic letters, 2015, 17, 1505-1508
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
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
1554873 CIFC20 H16 O2P 21 21 215.9724; 14.8969; 16.4863
90; 90; 90
1466.79Peraino, Nicholas J.; Wheeler, Kraig A.; Kerrigan, Nessan J.
Diastereoselective synthesis of γ-lactones through reaction of enediolates with α,β-unsaturated sulfoxonium salts.
Organic letters, 2015, 17, 1735-1737
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
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
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
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
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
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
1554900 CIFC14 H18 Cl N O8 SP 21 21 216.1403; 13.657; 20.719
90; 90; 90
1737.5Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
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
1554902 CIFC6 H12 Cl2 O2P 21 21 215.8932; 9.8358; 14.7998
90; 90; 90
857.86Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554912 CIFC20 H41 B2 F8 N5 OP 21 21 219.9728; 10.8425; 25.575
90; 90; 90
2765.4Mirabdolbaghi, Roya; Dudding, Travis
Expanding the forefront of strong organic Brønsted acids: proton-catalyzed hydroamination of unactivated alkenes and activation of Au(I) for alkyne hydroamination.
Organic letters, 2015, 17, 1930-1933
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
1554917 CIFC18 H16 F3 N OP 21 21 215.8836; 19.2027; 26.5181
90; 90; 90
2996Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
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
1554924 CIFC19 H29 F N2 O5 SiP 21 21 216.42; 8.0707; 40.1927
90; 90; 90
2082.54Istrate, Alena; Medvecky, Michal; Leumann, Christian J.
2'-Fluorination of tricyclo-DNA controls furanose conformation and increases RNA affinity.
Organic letters, 2015, 17, 1950-1953
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
1554930 CIFC16 H25 N O2 S3P 21 21 215.36225; 12.0412; 27.5363
90; 90; 90
1777.96Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
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
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
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
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
1554990 CIFC15 H13 N O4 SP 21 21 218.1609; 9.0398; 19.318
90; 90; 90
1425.1Liu, Yan-Kai; Li, Zhi-Long; Li, Ji-Yao; Feng, Huan-Xi; Tong, Zhi-Ping
Open-close: an alternative strategy to α-functionalization of lactone via enamine catalysis in one pot under mild conditions.
Organic letters, 2015, 17, 2022-2025
1554992 CIFC15 H13 N O3P 21 21 215.2776; 10.8907; 22.1326
90; 90; 90
1272.11Sun, Yao-Liang; Wei, Yin; Shi, Min
Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion
Organic Chemistry Frontiers, 2019, 6, 2420
1554997 CIFC21 H18 N4 O4 SP 21 21 216.0211; 16.1241; 20.634
90; 90; 90
2003.25Li, Shi-Wu; Du, Yu; Kang, Qiang
A chiral-at-metal asymmetric catalyzed vinylogous Michael addition of ortho-methyl aromatic nitro compounds for isoxazole derivative synthesis
Organic Chemistry Frontiers, 2019, 6, 2775
1555004 CIFC28 H32 F N O2P 21 21 218.03153; 10.686; 28.3689
90; 90; 90
2434.76Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555022 CIFC17 H22 O2P 21 21 218.6511; 11.009; 15.784
90; 90; 90
1503.3Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J.
Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.
Organic letters, 2015, 17, 2278-2281
1555052 CIFC15 H20 O5P 21 21 217.3936; 10.5735; 17.817
90; 90; 90
1392.9Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555057 CIFC21 H22 O11P 21 21 218.2302; 14.4554; 16.2394
90; 90; 90
1932.01Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555087 CIFC10 H9 F3 N2 OP 21 21 217.1385; 7.5039; 19.126
90; 90; 90
1024.5Wang, Xiaonan; Gao, Yuan; Wei, Zhonglin; Cao, Jungang; Liang, Dapeng; Lin, Yingjie; Duan, Haifeng
An enantioselective aza-Henry reaction of trifluoromethyl ketimines catalyzed by phase-transfer catalysts
Organic Chemistry Frontiers, 2019, 6, 3269
1555101 CIFC25 H22 F N O5P 21 21 218.9187; 14.6101; 16.5218
90; 90; 90
2152.8Bhattacharya, Aditya; mani Shukla, Pushpendra; Kumar Kaushik, Lalit; Maji, Biswajit
Synthesis of chromans and kinetic resolution of 2-aryl-3-nitro-2H-chromenes via the NHC-bound azolium homoenolate pathway
Organic Chemistry Frontiers, 2019, 6, 3523
1555108 CIFC9 H12 O4P 21 21 216.345; 8.9881; 15.108
90; 90; 90
861.6Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555110 CIFC26 H20 O3 SP 21 21 217.9759; 16.1628; 31.7213
90; 90; 90
4089.3Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan
A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds
Organic Chemistry Frontiers, 2019, 6, 3259
1555111 CIFC27 H21 N O3 SP 21 21 215.7472; 16.912; 22.0104
90; 90; 90
2139.34Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan
A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds
Organic Chemistry Frontiers, 2019, 6, 3259
1555112 CIFC19 H22 N2 OP 21 21 217.4987; 12.2482; 16.8063
90; 90; 90
1543.58Wong, Suet-Pick; Gan, Chew-Yan; Lim, Kuan-Hon; Ting, Kang-Nee; Low, Yun-Yee; Kam, Toh-Seok
Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon-Nitrogen Skeleton Derived from a Pericine Precursor.
Organic letters, 2015, 17, 3628-3631
1555126 CIFC13 H19 N O3 SP 21 21 217.789; 11.669; 15.029
90; 90; 90
1366Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555131 CIFC16 H9 N3 O2 SP 21 21 215.168; 15.6589; 15.9344
90; 90; 90
1289.49Recio, Javier; Pérez-Redondo, Adrián; Alvarez-Builla, Julio; Burgos, Carolina
Access to 2-substituted 1-pyridin-3-yl-β-carboline derivatives by intramolecular radical cyclization-ring opening-SNAr substitution
Organic Chemistry Frontiers, 2019, 6, 3300
1555134 CIFC20 H23 Br Cl N O4 SP 21 21 217.6751; 12.59; 22.275
90; 90; 90
2152.4Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555141 CIFC24 H21 N O3 SP 21 21 217.3838; 11.2551; 24.298
90; 90; 90
2019.3Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555148 CIFC43 H48 N O3 S2P 21 21 2111.13642; 14.74032; 46.2616
90; 90; 90
7594.04Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui
A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.
Organic letters, 2015, 17, 4128-4131
1555149 CIFC8 H8 N2 O4P 21 21 214.888; 9.8; 18.388
90; 90; 90
880.8Salahifar, Eslam; Nematollahi, Davood; Bayat, Mehdi; Mahyari, Amir; Amiri Rudbari, Hadi
Regioselective Green Electrochemical Approach to the Synthesis of Nitroacetaminophen Derivatives.
Organic letters, 2015, 17, 4666-4669
1555153 CIFC17 H16 O2P 21 21 217.3872; 10.8747; 16.4977
90; 90; 90
1325.32Cecchini, Chiara; Cera, Gianpiero; Lanzi, Matteo; Marchiò, Luciano; Malacria, Max; Maestri, Giovanni
Diastereoselective bicyclization of enynols via gold catalysis
Organic Chemistry Frontiers, 2019, 6, 3584
1555160 CIFC16 H14 O5P 21 21 218.594; 11.8962; 13.1105
90; 90; 90
1340.36Sun, Zhaocui; Zhu, Nailiang; Zhou, Man; Huo, Xiaowei; Wu, Haifeng; Tian, Yu; Yang, Junshan; Ma, Guoxu; Yang, Yan-Long; Xu, Xudong
Clavipines A‒C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes
Organic Chemistry Frontiers, 2019, 6, 3759
1555169 CIFC25 H22 N2 O6 SiP 21 21 215.9864; 18.2027; 21.5323
90; 90; 90
2346.35Vale, João R.; Valkonen, Arto; Afonso, Carlos A. M.; Candeias, Nuno R.
Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes
Organic Chemistry Frontiers, 2019, 6, 3793
1555170 CIFC22 H26 O7P 21 21 219.136; 10.6809; 42.2825
90; 90; 90
4126Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido
Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.
Organic letters, 2015, 17, 4940-4943
1555171 CIFC23 H28 O7P 21 21 218.5586; 9.2119; 27.3349
90; 90; 90
2155.11Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido
Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.
Organic letters, 2015, 17, 4940-4943
1555174 CIFC22 H30.66667 O4.33333P 21 21 2112.7263; 18.5197; 24.0727
90; 90; 90
5673.6Wang, Jia-Peng; Shu, Yan; Liu, Shi-Xi; Hu, Jun-Tao; Sun, Cheng-Tong; Zhou, Hao; Gan, Dong; Cai, Xue-Yun; Pu, Wei; Cai, Le; Ding, Zhong-Tao
Expanstines A–D: four unusual isoprenoid epoxycyclohexenones generated by Penicillium expansum YJ-15 fermentation and photopromotion
Organic Chemistry Frontiers, 2019, 6, 3839
1555183 CIFC48 H38 Cl2 N4 O4 S4P 21 21 2112.652; 19.153; 22.403
90; 90; 90
5428.8Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang
Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation.
Organic letters, 2015, 17, 4188-4191
1555187 CIFC19 H21 Cl2 N O2 SP 21 21 216.1472; 11.724; 27.834
90; 90; 90
2006Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555192 CIFC19 H20 Cl N O2 SP 21 21 218.434; 9.511; 23.843
90; 90; 90
1913Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555194 CIFC25 H19 N3 OP 21 21 217.2944; 14.078; 19.047
90; 90; 90
1955.9Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.
Organic letters, 2015, 17, 4066-4069
1555221 CIFC32 H22.67 N2 O2.33P 21 21 2110.41941; 18.297; 36.8632
90; 90; 90
7027.75Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555222 CIFC32 H22 N2 O2P 21 21 217.9491; 16.7592; 18.1848
90; 90; 90
2422.6Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555226 CIFC28 H24 N2 O3 SP 21 21 218.9629; 14.1297; 18.6198
90; 90; 90
2358.1Wang, Linqing; Yang, Dongxu; Li, Dan; Liu, Xihong; Zhao, Qian; Zhu, Ranran; Zhang, Bangzhi; Wang, Rui
Catalytic Asymmetric [3 + 2] Cyclization Reactions of 3-Isothiocyanato Oxindoles and Alkynyl Ketones Via an in Situ Generated Magnesium Catalyst.
Organic letters, 2015, 17, 4260-4263
1555236 CIFC14 H17 F O2P 21 21 215.8616; 11.0435; 18.6965
90; 90; 90
1210.27Navuluri, Chandrasekhar; Charette, André B
Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.
Organic letters, 2015, 17, 4288-4291
1555249 CIFC40 H34 Br N3 O3P 21 21 2112.8306; 13.8096; 19.054
90; 90; 90
3376.1Jing, Changcheng; Xing, Dong; Hu, Wenhao
Catalytic Asymmetric Four-Component Reaction for the Rapid Construction of 3,3-Disubstituted 3-Indol-3'-yloxindoles.
Organic letters, 2015, 17, 4336-4339
1555281 CIFC43 H69 N3 O12P 21 21 2111.226; 12.666; 33.431
90; 90; 90
4753.5Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.
γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.
Organic letters, 2015, 17, 4738-4741
1555308 CIFC17 H13 N O3P 21 21 217.1386; 8.0009; 23.6032
90; 90; 90
1348.1Cheng, Tanyu; Ye, Qunqun; Zhao, Qiankun; Liu, Guohua
Dynamic Kinetic Resolution of Phthalides via Asymmetric Transfer Hydrogenation: A Strategy Constructs 1,3-Distereocentered 3-(2-Hydroxy-2-arylethyl)isobenzofuran-1(3H)-one.
Organic letters, 2015, 17, 4972-4975
1555314 CIFC20 H18 F3 N3 O5P 21 21 218.1216; 11.5944; 21.1982
90; 90; 90
1996.1Henderson, Alexander S.; Medina, Sandra; Bower, John F.; Galan, M. Carmen
Nucleophilic Aromatic Substitution (SNAr) as an Approach to Challenging Carbohydrate-Aryl Ethers.
Organic letters, 2015, 17, 4846-4849
1555339 CIFC22 H28 O3P 21 21 2111.3754; 11.9359; 14.185
90; 90; 90
1925.98Liao, Hai-Bing; Lei, Chun; Gao, Li-Xin; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Two Enantiomeric Pairs of Meroterpenoids from Rhododendron capitatum.
Organic letters, 2015, 17, 5040-5043
1555343 CIFC13 H21 N O2P 21 21 216.0749; 8.2818; 25.017
90; 90; 90
1258.6Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.
Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.
Organic letters, 2015, 17, 5204-5207
1555344 CIFC11 H19 N O2P 21 21 2110.7069; 10.8672; 19.656
90; 90; 90
2287.1Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.
Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.
Organic letters, 2015, 17, 5204-5207
1555347 CIFC8 H11 N O2P 21 21 216.742; 7.2944; 15.8577
90; 90; 90
779.86Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.
Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.
Organic letters, 2015, 17, 5204-5207
1555354 CIFC18 H32 N2 OP 21 21 215.287; 9.4826; 34.033
90; 90; 90
1706.23Bosch, Caroline; Fiser, Béla; Gómez-Bengoa, Enrique; Bradshaw, Ben; Bonjoch, Josep
Approach to cis-Phlegmarine Alkaloids via Stereodivergent Reduction: Total Synthesis of (+)-Serratezomine E and Putative Structure of (-)-Huperzine N.
Organic letters, 2015, 17, 5084-5087
1555355 CIFC24 H24 Br N O4P 21 21 216.6742; 12.874; 25.688
90; 90; 90
2207.2Das, Tapas; Saha, Prasenjit; Singh, Vinod K.
Silver(I)-Ferrophox Catalyzed Enantioselective Desymmetrization of Cyclopentenedione: Synthesis of Highly Substituted Bicyclic Pyrrolidines.
Organic letters, 2015, 17, 5088-5091
1555358 CIFC25 H26 F6 N3 P PdP 21 21 219.6947; 12.5617; 21.062
90; 90; 90
2565Álvarez-Casao, Yolanda; Monge, David; Álvarez, Eleuterio; Fernández, Rosario; Lassaletta, José M
Pyridine-Hydrazones as N,N'-Ligands in Asymmetric Catalysis: Pd(II)-Catalyzed Addition of Boronic Acids to Cyclic Sulfonylketimines.
Organic letters, 2015, 17, 5104-5107
1555371 CIFC14 H11 N O2 S2P 21 21 217.5169; 10.5263; 16.5993
90; 90; 90
1313.42Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.
Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.
Organic letters, 2015, 17, 5340-5343
1555372 CIFC15 H17 N O4 SP 21 21 217.7171; 7.9486; 23.816
90; 90; 90
1460.88Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.
Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.
Organic letters, 2015, 17, 5340-5343
1555374 CIFC14 H11 N O3 SP 21 21 217.5472; 10.3052; 16.2327
90; 90; 90
1262.5Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.
Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.
Organic letters, 2015, 17, 5340-5343
1555375 CIFC11 H11 N O2 SP 21 21 218.0916; 9.4218; 13.8016
90; 90; 90
1052.2Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.
Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.
Organic letters, 2015, 17, 5340-5343
1555376 CIFC24 H21 Br O6P 21 21 216.625; 10.223; 31.029
90; 90; 90
2101.5Liang, Zhi-Qin; Wang, Dong-Ling; Zhang, Han-Ming; Ye, Song
Enantioselective Synthesis of Bicyclic δ-Lactones via N-Heterocyclic Carbene-Catalyzed Cascade Reaction.
Organic letters, 2015, 17, 5140-5143
1555387 CIFC37 H42 N4 O6P 21 21 217.8202; 15.433; 28.4386
90; 90; 90
3432.2Chingle, Ramesh; Lubell, William D.
Azopeptides: Synthesis and Pericyclic Chemistry.
Organic letters, 2015, 17, 5400-5403
1555391 CIFC48 H70 Cl I2 N7 OP 21 21 2111.7863; 15.6266; 27.3025
90; 90; 90
5028.57Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.
Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.
Organic letters, 2015, 17, 5740-5743
1555396 CIFC13 H20 N2 O7P 21 21 217.5247; 13.1309; 15.066
90; 90; 90
1488.61Habibian, Maryam; Martínez-Montero, Saúl; Portella, Guillem; Chua, Zhijie; Bohle, D. Scott; Orozco, Modesto; Damha, Masad J.
Seven-Membered Ring Nucleoside Analogues: Stereoselective Synthesis and Studies on Their Conformational Properties.
Organic letters, 2015, 17, 5416-5419
1555399 CIFC18 H22 O3P 21 21 217.5988; 8.4424; 21.953
90; 90; 90
1408.33Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond
Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.
Organic letters, 2015, 17, 5432-5435
1555400 CIFC20 H23 N O3P 21 21 217.2672; 12.3762; 18.5597
90; 90; 90
1669.27Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond
Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.
Organic letters, 2015, 17, 5432-5435
1555407 CIFC24 H21 N O6 SP 21 21 217.7963; 11.5859; 23.086
90; 90; 90
2085.3Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555409 CIFC20 H19 N O5 SP 21 21 217.7017; 8.4118; 27.288
90; 90; 90
1767.9Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555412 CIFC17 H12 Br F2 N O5 SP 21 21 216.8957; 12.551; 22.629
90; 90; 90
1958.5Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555414 CIFC19 H17 Br Cl N O5 SP 21 21 219.155; 9.47; 23.095
90; 90; 90
2002.3Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555415 CIFC14 H22 O4P 21 21 216.5953; 9.079; 21.403
90; 90; 90
1281.6Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong
Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.
Organic letters, 2015, 17, 5480-5483
1555416 CIFC18 H28 O4 SiP 21 21 217.2691; 11.4811; 21.668
90; 90; 90
1808.4Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong
Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.
Organic letters, 2015, 17, 5480-5483
1555421 CIFC24 H31 N O5 SP 21 21 215.8376; 10.6992; 37.5454
90; 90; 90
2345Serpier, Fabien; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain
Access to Polyfunctionalized Chiral Piperidines through Enantioselective Addition-Carbocyclization Cascade Reaction Catalyzed by a Rhodium(I)-Diene Complex.
Organic letters, 2015, 17, 5496-5499
1555437 CIFC25 H28 N4 O5P 21 21 218.2785; 9.2956; 29.7576
90; 90; 90
2289.96Yang, Van-Wei; Hong, Bor-Cherng; Kao, Hsin-Kai; Tu, Ting-Hsun; Shen, Jiun-Yi; Chen, Chi-Lin; Lee, Gene-Hsiang; Chou, Pi-Tai
One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment.
Organic letters, 2015, 17, 5816-5819
1555446 CIFC18 H22 O2P 21 21 219.0068; 10.478; 16.4734
90; 90; 90
1554.65Lai, Zengwei; Wang, Zhaobin; Sun, Jianwei
Organocatalytic Asymmetric Nucleophilic Addition to o-Quinone Methides by Alcohols.
Organic letters, 2015, 17, 6058-6061
1555453 CIFC38 H54 O5P 21 21 2110.0955; 13.4185; 24.927
90; 90; 90
3376.8Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555467 CIFC20 H14 O2P 21 21 217.3238; 9.814; 19.747
90; 90; 90
1419.3Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555495 CIFC24 H22 Br N3 O5.5P 21 21 2112.8376; 12.9227; 14.0967
90; 90; 90
2338.59Kumarswamyreddy, Nandarapu; Kesavan, Venkitasamy
Enantioselective Synthesis of Dihydrospiro[indoline-3,4'-pyrano[2,3-c]pyrazole] Derivatives via Michael/Hemiketalization Reaction.
Organic letters, 2016, 18, 1354-1357
1555496 CIFC25 H22 F N O2P 21 21 219.56524; 18.64102; 22.57118
90; 90; 90
4024.57Ošeka, Maksim; Kimm, Mariliis; Kaabel, Sandra; Järving, Ivar; Rissanen, Kari; Kanger, Tõnis
Asymmetric Organocatalytic Wittig [2,3]-Rearrangement of Oxindoles.
Organic letters, 2016, 18, 1358-1361
1555500 CIFC19 H26 O3P 21 21 216.43415; 13.9695; 18.8234
90; 90; 90
1691.88Lin, Han; Xiao, Li-Jun; Zhou, Min-Jie; Yu, Hong-Ming; Xie, Jian-Hua; Zhou, Qi-Lin
Enantioselective Approach to (-)-Hamigeran B and (-)-4-Bromohamigeran B via Catalytic Asymmetric Hydrogenation of Racemic Ketone To Assemble the Chiral Core Framework.
Organic letters, 2016, 18, 1434-1437
1555505 CIFC164 H260 N4 O75 S3P 21 21 2118.0825; 18.5554; 56.7015
90; 90; 90
19024.9Inouye, Masahiko; Yoshizawa, Atsushi; Shibata, Mari; Yonenaga, Yuki; Fujimoto, Kazuhisa; Sakata, Takuma; Matsumoto, Shinya; Shiro, Motoo
Cyclodextrin-Isolated Alkynylpyrenes as UV-Stable and Blue-Light-Emitting Molecules Even in Condensed States.
Organic letters, 2016, 18, 1960-1963
1555509 CIFC17 H18 Cl N O5P 21 21 216.891; 11.883; 20.413
90; 90; 90
1671.5Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555511 CIFC17 H19 N O5P 21 21 217.7825; 12.1682; 16.9656
90; 90; 90
1606.63Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555525 CIFC23 H39 N O3 S SiP 21 21 2111.2183; 17.958; 25.733
90; 90; 90
5184.1Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555526 CIFC25 H37 N3 O3P 21 21 218.174; 12.797; 21.823
90; 90; 90
2282.7Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555528 CIFC18 H31 N O5P 21 21 217.71375; 8.88494; 28.0459
90; 90; 90
1922.16Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555542 CIFC20 H26 O3P 21 21 219.7169; 10.1381; 17.5286
90; 90; 90
1726.76Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555546 CIFC28 H25 N O2P 21 21 215.9977; 8.669; 42.0392
90; 90; 90
2185.79Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555553 CIFC18 H22 F N O4P 21 21 219.7821; 11.5835; 14.8591
90; 90; 90
1683.7Zhu, Luyi; Chen, Qiliang; Shen, Dan; Zhang, Weihao; Shen, Cong; Zeng, Xiaofei; Zhong, Guofu
Enantioselective Construction of Spirocyclic Oxindole Derivatives with Multiple Stereocenters via an Organocatalytic Michael/Aldol/Hemiacetalization Cascade Reaction.
Organic letters, 2016, 18, 2387-2390
1555564 CIFC16 H24 N2 O3 SP 21 21 218.6938; 9.8115; 18.943
90; 90; 90
1615.8Crossley, Steven W. M.; Martinez, Ruben M.; Guevara-Zuluaga, Sebastián; Shenvi, Ryan A.
Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol.
Organic letters, 2016, 18, 2620-2623
1555572 CIFC25 H34 N2 O4P 21 21 216.0956; 15.5691; 24.6358
90; 90; 90
2338.01Nagaraju, Karre; Chegondi, Rambabu; Chandrasekhar, Srivari
Expanding Diversity without Protecting Groups: (+)-Sclareolide to Indolosesquiterpene Alkaloid Mycoleptodiscin A and Analogues.
Organic letters, 2016, 18, 2684-2687
1555575 CIFC16 H15 F3 N2P 21 21 216.37164; 8.13751; 26.6535
90; 90; 90
1381.96Ma, Wenpeng; Chen, Fei; Liu, Youran; He, Yan-Mei; Fan, Qing-Hua
Ruthenium-Catalyzed Enantioselective Hydrogenation of 1,8-Naphthyridine Derivatives.
Organic letters, 2016, 18, 2730-2733
1555585 CIFC15 H23 N O2 SP 21 21 216.5067; 10.2546; 22.3875
90; 90; 90
1493.77Kubiak, 2nd, Robert W; Mighion, Jeffrey D.; Wilkerson-Hill, Sidney M; Alford, Joshua S.; Yoshidomi, Tetsushi; Davies, Huw M. L.
Enantioselective Intermolecular C-H Functionalization of Allylic and Benzylic sp(3) C-H Bonds Using N-Sulfonyl-1,2,3-triazoles.
Organic letters, 2016, 18, 3118-3121
1555587 CIFC22 H24 Br N O5P 21 21 218.662; 9.2342; 26.0487
90; 90; 90
2083.55Das, Saikat; Chakrabarty, Shyamal; Daniliuc, Constantin G.; Studer, Armido
Tetrahydroquinolines via Stereospecific [3 + 3]-Annulation of Donor-Acceptor Cyclopropanes with Nitrosoarenes.
Organic letters, 2016, 18, 2784-2787
1555599 CIFC19 H20 N2 OP 21 21 216.8328; 11.6515; 19.2975
90; 90; 90
1536.32Rahman, M. Toufiqur; Deschamps, Jeffrey R.; Imler, Gregory H.; Schwabacher, Alan W.; Cook, James M.
Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide.
Organic letters, 2016, 18, 4174-4177
1555616 CIFC49 H25 F9P 21 21 219.7462; 17.2319; 23.8323
90; 90; 90
4002.5Rao, M. Rajeswara; Johnson, Shea; Perepichka, Dmitrii F.
Aromatization of Benzannulated Perylene-3,9-diones: Unexpected Photophysical Properties and Reactivity.
Organic letters, 2016, 18, 3574-3577
1555617 CIFC26 H30 N4 O5P 21 21 219.7084; 15.1043; 16.6406
90; 90; 90
2440.2Wang, Kai-Bo; Li, Da-Hong; Hu, Ping; Wang, Wen-Jing; Lin, Clement; Wang, Jian; Lin, Bin; Bai, Jiao; Pei, Yue-Hu; Jing, Yong-Kui; Li, Zhan-Lin; Yang, Danzhou; Hua, Hui-Ming
A Series of β-Carboline Alkaloids from the Seeds of Peganum harmala Show G-Quadruplex Interactions.
Organic letters, 2016, 18, 3398-3401
1555622 CIFC19 H15 N O SP 21 21 215.5711; 6.5999; 40.0657
90; 90; 90
1473.16Ahlemeyer, Nicholas A.; Birman, Vladimir B.
Asymmetric Catalytic Synthesis of Thiochromenes via an Acyl Transfer-Initiated Cascade.
Organic letters, 2016, 18, 3454-3457
1555623 CIFC24 H32 O3P 21 21 217.9418; 9.0278; 28.012
90; 90; 90
2008.4Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555625 CIFC28 H38 O8P 21 21 218.352; 14.9946; 40.87
90; 90; 90
5118.4Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555626 CIFC31 H46 O8P 21 21 217.4728; 11.6974; 33.552
90; 90; 90
2932.9Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555628 CIFC28 H40 O7P 21 21 2113.3481; 15.278; 36.973
90; 90; 90
7540Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555629 CIFC28 H44 O9P 21 21 219.3211; 11.4032; 26.089
90; 90; 90
2773Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555635 CIFC20 H26 N2 O2P 21 21 219.01057; 10.9727; 17.5326
90; 90; 90
1733.45Tokuda, Ryoko; Okamoto, Yoshiki; Koyama, Tetsuya; Kogure, Noriyuki; Kitajima, Mariko; Takayama, Hiromitsu
Asymmetric Total Synthesis of Kopsiyunnanine K, a Monoterpenoid Indole Alkaloid with a Rearranged Skeleton.
Organic letters, 2016, 18, 3490-3493
1555638 CIFC41 H26P 21 21 219.8499; 11.1882; 24.6237
90; 90; 90
2713.6Oyama, Hiromi; Akiyama, Midori; Nakano, Koji; Naito, Masanobu; Nobusawa, Kazuyuki; Nozaki, Kyoko
Synthesis and Properties of [7]Helicene-like Compounds Fused with a Fluorene Unit.
Organic letters, 2016, 18, 3654-3657
1555645 CIFC28 H29 N O2P 21 21 215.0975; 10.807; 40.2707
90; 90; 90
2218.46Li, Wenbo; Yu, Xiuzhao; Yue, Zhenting; Zhang, Junliang
Asymmetric Construction of 2,3-Dihydroisoxazoles via an Organocatalytic Formal [3 + 2] Cycloaddition of Enynes with N-Hydroxylamines.
Organic letters, 2016, 18, 3972-3975
1555646 CIFC27 H22 Cl2 O6P 21 21 217.2743; 10.1737; 32.241
90; 90; 90
2386Ashtekar, Kumar Dilip; Ding, Xinliang; Toma, Edmond; Sheng, Wei; Gholami, Hadi; Rahn, Christopher; Reed, Paul; Borhan, Babak
Mechanistically Inspired Route toward Hexahydro-2H-chromenes via Consecutive [4 + 2] Cycloadditions.
Organic letters, 2016, 18, 3976-3979
1555647 CIFC31 H32 Cl4 O8P 21 21 2110.9256; 14.7077; 19.6645
90; 90; 90
3159.9Ashtekar, Kumar Dilip; Ding, Xinliang; Toma, Edmond; Sheng, Wei; Gholami, Hadi; Rahn, Christopher; Reed, Paul; Borhan, Babak
Mechanistically Inspired Route toward Hexahydro-2H-chromenes via Consecutive [4 + 2] Cycloadditions.
Organic letters, 2016, 18, 3976-3979
1555660 CIFC20 H20 O6P 21 21 2110.2949; 10.4128; 16.2831
90; 90; 90
1745.53Zhou, Jinchuan; Zhang, Jiaozhen; Li, Ruijuan; Liu, Jun; Fan, Peihong; Li, Yi; Ji, Mei; Dong, Yiwen; Yuan, Huiqing; Lou, Hongxiang
Hapmnioides A-C, Rearranged Labdane-Type Diterpenoids from the Chinese Liverwort Haplomitrium mnioides.
Organic letters, 2016, 18, 4274-4276
1555665 CIFC30 H46 O3P 21 21 216.3412; 17.9097; 23.6648
90; 90; 90
2687.59Zhang, Ya-Long; Chen, Chen; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Zhang, Can; Sun, Hong-Bin; Luo, Jian-Guang; Kong, Ling-Yi
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Organic letters, 2016, 18, 4068-4071
1555666 CIFC45 H68 O6P 21 21 219.6502; 13.9527; 31.7405
90; 90; 90
4273.7Zhang, Ya-Long; Chen, Chen; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Zhang, Can; Sun, Hong-Bin; Luo, Jian-Guang; Kong, Ling-Yi
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Organic letters, 2016, 18, 4068-4071
1555668 CIFC30 H46 O3P 21 21 219.9104; 10.8418; 26.6369
90; 90; 90
2862.04Zhang, Ya-Long; Chen, Chen; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Zhang, Can; Sun, Hong-Bin; Luo, Jian-Guang; Kong, Ling-Yi
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Organic letters, 2016, 18, 4068-4071
1555669 CIFC30 H46 O3P 21 21 2111.9618; 20.1271; 23.2612
90; 90; 90
5600.28Zhang, Ya-Long; Chen, Chen; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Zhang, Can; Sun, Hong-Bin; Luo, Jian-Guang; Kong, Ling-Yi
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Organic letters, 2016, 18, 4068-4071
1555677 CIFC14 H14 N2 O4P 21 21 216.7657; 12.1602; 16.0507
90; 90; 90
1320.53Mondal, Mukulesh; Wheeler, Kraig A.; Kerrigan, Nessan J.
Alkaloid-Catalyzed Enantioselective [3 + 2] Cycloaddition of Ketenes and Azomethine Imines.
Organic letters, 2016, 18, 4108-4111
1555678 CIFC14 H16 N2 O3P 21 21 216.7037; 8.7886; 21.923
90; 90; 90
1291.62Mondal, Mukulesh; Wheeler, Kraig A.; Kerrigan, Nessan J.
Alkaloid-Catalyzed Enantioselective [3 + 2] Cycloaddition of Ketenes and Azomethine Imines.
Organic letters, 2016, 18, 4108-4111
1555687 CIFC16 H23 N O2P 21 21 217.4804; 10.4902; 18.4048
90; 90; 90
1444.24Ma, Donghui; Zhong, Zhuliang; Liu, Zaimin; Zhang, Mingjie; Xu, Shiyan; Xu, Dengyu; Song, Dengpeng; Xie, Xingang; She, Xuegong
Protecting-Group-Free Total Synthesis of (-)-Lycopodine via Phosphoric Acid Promoted Alkyne Aza-Prins Cyclization.
Organic letters, 2016, 18, 4328-4331
1555688 CIFC16 H23 N O2P 21 21 2110.9468; 13.1316; 19.8805
90; 90; 90
2857.8Ma, Donghui; Zhong, Zhuliang; Liu, Zaimin; Zhang, Mingjie; Xu, Shiyan; Xu, Dengyu; Song, Dengpeng; Xie, Xingang; She, Xuegong
Protecting-Group-Free Total Synthesis of (-)-Lycopodine via Phosphoric Acid Promoted Alkyne Aza-Prins Cyclization.
Organic letters, 2016, 18, 4328-4331
1555695 CIFC19 H19 Cl O3P 21 21 218.4147; 9.8374; 20.9238
90; 90; 90
1732Su, Yan; Li, Qing-Fang; Zhao, Yu-Ming; Gu, Peiming
Preparation of Optically Active cis-Cyclopropane Carboxylates: Cyclopropanation of α-Silyl Stryenes with Aryldiazoacetates and Desilylation of the Resulting Silyl Cyclopropanes.
Organic letters, 2016, 18, 4356-4359
1555696 CIFC21 H25 Br O2 SiP 21 21 218.9734; 9.5887; 24.3831
90; 90; 90
2098Su, Yan; Li, Qing-Fang; Zhao, Yu-Ming; Gu, Peiming
Preparation of Optically Active cis-Cyclopropane Carboxylates: Cyclopropanation of α-Silyl Stryenes with Aryldiazoacetates and Desilylation of the Resulting Silyl Cyclopropanes.
Organic letters, 2016, 18, 4356-4359
1555700 CIFC23 H43 N2 O10 P SP 21 21 2110.3757; 11.5557; 24.7257
90; 90; 90
2964.57Lin, Long-Zhi; Fang, Jim-Min
Total Synthesis of Anti-Influenza Agents Zanamivir and Zanaphosphor via Asymmetric Aza-Henry Reaction.
Organic letters, 2016, 18, 4400-4403
1555701 CIFC16 H30 N2 O7 SP 21 21 2110.1789; 11.9132; 18.0755
90; 90; 90
2191.89Lin, Long-Zhi; Fang, Jim-Min
Total Synthesis of Anti-Influenza Agents Zanamivir and Zanaphosphor via Asymmetric Aza-Henry Reaction.
Organic letters, 2016, 18, 4400-4403
1555702 CIFC22 H38 N2 O9 SP 21 21 2110.2553; 11.3826; 23.6017
90; 90; 90
2755.07Lin, Long-Zhi; Fang, Jim-Min
Total Synthesis of Anti-Influenza Agents Zanamivir and Zanaphosphor via Asymmetric Aza-Henry Reaction.
Organic letters, 2016, 18, 4400-4403
1555703 CIFC16 H21 N O2P 21 21 218.5903; 9.1195; 17.5588
90; 90; 90
1375.54Tang, Yu; Xiong, Juan; Zhang, Jing-Jing; Wang, Wei; Zhang, Hai-Yan; Hu, Jin-Feng
Annotinolides A-C, Three Lycopodane-Derived 8,5-Lactones with Polycyclic Skeletons from Lycopodium annotinum.
Organic letters, 2016, 18, 4376-4379
1555704 CIFC16 H21 N O2P 21 21 218.7114; 9.1691; 16.9047
90; 90; 90
1350.27Tang, Yu; Xiong, Juan; Zhang, Jing-Jing; Wang, Wei; Zhang, Hai-Yan; Hu, Jin-Feng
Annotinolides A-C, Three Lycopodane-Derived 8,5-Lactones with Polycyclic Skeletons from Lycopodium annotinum.
Organic letters, 2016, 18, 4376-4379
1555705 CIFC16 H19 N O4P 21 21 217.8847; 12.731; 13.5189
90; 90; 90
1357.03Tang, Yu; Xiong, Juan; Zhang, Jing-Jing; Wang, Wei; Zhang, Hai-Yan; Hu, Jin-Feng
Annotinolides A-C, Three Lycopodane-Derived 8,5-Lactones with Polycyclic Skeletons from Lycopodium annotinum.
Organic letters, 2016, 18, 4376-4379
1555706 CIFC16 H21 N O2P 21 21 218.7313; 10.0431; 14.6801
90; 90; 90
1287.29Tang, Yu; Xiong, Juan; Zhang, Jing-Jing; Wang, Wei; Zhang, Hai-Yan; Hu, Jin-Feng
Annotinolides A-C, Three Lycopodane-Derived 8,5-Lactones with Polycyclic Skeletons from Lycopodium annotinum.
Organic letters, 2016, 18, 4376-4379
1555711 CIFC14 H7 Br N2 O4P 21 21 213.8804; 7.5188; 43.727
90; 90; 90
1275.8Verma, Ajay; Kumar, Sangit
Selective Oxidative Decarbonylative Cleavage of Unstrained C(sp(3))-C(sp(2)) Bond: Synthesis of Substituted Benzoxazinones.
Organic letters, 2016, 18, 4388-4391
1555720 CIFC29.64 H34.56 O10.36P 21 21 216.9086; 13.0711; 29.2663
90; 90; 90
2642.8Zhou, Ming; Liu, Ye; Song, Jian; Peng, Xiao-Gang; Cheng, Qi; Cao, Hui; Xiang, Ming; Ruan, Han-Li
Schincalide A, a Schinortriterpenoid with a Tricyclo[5.2.1.0(1,6)]decane-Bridged System from the Stems and Leaves of Schisandra incarnate.
Organic letters, 2016, 18, 4558-4561
1555725 CIFC27 H16 F N OP 21 21 217.3458; 11.9086; 21.862
90; 90; 90
1912.45Cai, Zhong-Jian; Li, Fang-Hui; Wang, Shun-Yi; Ji, Shun-Jun
Palladium-Catalyzed Cascade Arene/Alkyne Annulation: Synthesis of Fluorene-Benzoxazine Derivatives.
Organic letters, 2016, 18, 4810-4813
1555741 CIFC15 H23 N O3P 21 21 218.5731; 9.2969; 17.1079
90; 90; 90
1363.56Xu, Shiyan; Zhang, Jing; Ma, Donghui; Xu, Dengyu; Xie, Xingang; She, Xuegong
Asymmetric Total Synthesis of (-)-Lycospidine A.
Organic letters, 2016, 18, 4682-4685
1555747 CIFC19 H21 N O4P 21 21 218.4444; 10.0554; 18.0941
90; 90; 90
1536.4Garcia, Alfredo; Drown, Bryon S.; Hergenrother, Paul J.
Access to a Structurally Complex Compound Collection via Ring Distortion of the Alkaloid Sinomenine.
Organic letters, 2016, 18, 4852-4855
1555751 CIFC23 H29 Cl3 N2 O3 SP 21 21 2110.8104; 11.1726; 21.1349
90; 90; 90
2552.68Zhang, Juan; Chen, Zhi-Xiong; Du, Ting; Li, Bing; Gu, Yonghong; Tian, Shi-Kai
Aryne-Mediated [2,3]-Sigmatropic Rearrangement of Tertiary Allylic Amines.
Organic letters, 2016, 18, 4872-4875
1555756 CIFC24 H23 N O3P 21 21 216.9578; 11.041; 24.685
90; 90; 90
1896.3Huang, Yu-Wen; Frontier, Alison J.
Nazarov Cyclization/Internal Redox Cyclization Sequence for the Synthesis of N-Heterocyclic Bridged Ring Systems.
Organic letters, 2016, 18, 4896-4899
1555767 CIFC19 H21 N O2P 21 21 215.3836; 31.775; 9.5511
90; 90; 90
1633.85Lynch, Denis; Deasy, Rebecca E.; Clarke, Leslie-Ann; Slattery, Catherine N.; Khandavilli, U. B. Rao; Lawrence, Simon E.; Maguire, Anita R.; Magnus, Nicholas A.; Moynihan, Humphrey A.
Exploring the Scope of Asymmetric Synthesis of β-Hydroxy-γ-lactams via Noyori-type Reductions.
Organic letters, 2016, 18, 4978-4981
1555775 CIFC9 H8 Cl N O2P 21 21 215.961; 7.819; 20.316
90; 90; 90
946.9Gao, Mingchun; Xu, Bin
Copper Nitrate Mediated Regio- and Stereoselective Difunctionalization of Alkynes: A Direct Approach to α-Chloro-β-nitroolefins.
Organic letters, 2016, 18, 4746-4749
1555776 CIFC10 H8 N2 O2 SP 21 21 216.758; 8.245; 18.741
90; 90; 90
1044.2Gao, Mingchun; Xu, Bin
Copper Nitrate Mediated Regio- and Stereoselective Difunctionalization of Alkynes: A Direct Approach to α-Chloro-β-nitroolefins.
Organic letters, 2016, 18, 4746-4749
1555778 CIFC21 H18 O2P 21 21 2112.151; 23.564; 5.864
90; 90; 90
1679Li, Jingfu; Chang, Wenju; Ren, Wenlong; Dai, Jie; Shi, Yian
Palladium-Catalyzed Highly Regio- and Enantioselective Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2016, 18, 5456-5459
1555800 CIFC17 H13 N OP 21 21 217.2723; 12.1743; 13.9939
90; 90; 90
1239Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Wu, Yan-Dong; Wu, An-Xin
Substrates as Electron-Donor Precursors: Synthesis of Naphtho-Fused Oxindoles via Benzannulation of 2-Halobenzaldehydes and Indolin-2-ones.
Organic letters, 2016, 18, 5232-5235
1555801 CIFC21 H17 Br O2P 21 21 218.2974; 13.684; 15.775
90; 90; 90
1791.12Chen, Tao; Li, Yi-Fan; An, Yang; Zhang, Fu-Min
Iron-Catalyzed α-Arylation of Deoxybenzoins with Arenes through an Oxidative Dehydrogenative Approach.
Organic letters, 2016, 18, 4754-4757
1555808 CIFC24 H19 F N2 O3P 21 21 215.86821; 16.6995; 20.8172
90; 90; 90
2040.01Guo, Songsong; Liu, Xiaohua; Shen, Bin; Lin, Lili; Feng, Xiaoming
Organocatalytic Asymmetric Cascade Reaction of 2-Hydroxyphenyl-Substituted Enones and Isocyanates To Construct 1,3-Benzoxazin-2-ones.
Organic letters, 2016, 18, 5070-5073
1555817 CIFC19 H15 Br O4P 21 21 216.86; 10.8272; 22.448
90; 90; 90
1667.3Zhang, Ming-Liang; Wu, Zhi-Jun; Zhao, Jian-Qiang; Luo, Yuan; Xu, Xiao-Ying; Zhang, Xiao-Mei; Yuan, Wei-Cheng
Michael Addition-Lactonization of Arylacetyl Phosphonate to β,γ-Unsaturated α-Keto Esters for the Synthesis of Chiral syn-3,4-Dihydropyranones and 5,6-Dihydropyranones.
Organic letters, 2016, 18, 5110-5113
1555819 CIFC30 H25 O2 P SeP 21 21 217.48; 16.779; 19.319
90; 90; 90
2424.7Maekawa, Yuuki; Maruyama, Toshifumi; Murai, Toshiaki
Sequential Deprotonation-Alkylation of Binaphthyloxy-Substituted Phosphonochalcogenoates: Chiral Tri- and Tetrasubstituted Carbon Centers Adjacent to a Phosphorus Atom.
Organic letters, 2016, 18, 5264-5267
1555820 CIFC36 H27 O4 P SeP 21 21 2111.8545; 15.6874; 16.0313
90; 90; 90
2981.3Maekawa, Yuuki; Maruyama, Toshifumi; Murai, Toshiaki
Sequential Deprotonation-Alkylation of Binaphthyloxy-Substituted Phosphonochalcogenoates: Chiral Tri- and Tetrasubstituted Carbon Centers Adjacent to a Phosphorus Atom.
Organic letters, 2016, 18, 5264-5267
1555838 CIFC34 H33 Cl N2 O3P 21 21 217.61287; 18.37433; 18.9503
90; 90; 90
2650.79Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319

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