Crystallography Open Database

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Searching year of publication is 2015

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1553071 CIFC23 H16 OP 1 21 111.008; 7.5883; 19.571
90; 90.988; 90
1634.6Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat
Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds
Organic Chemistry Frontiers, 2015, 2, 312
1553072 CIFC22 H23 N O2P -19.1264; 9.7169; 10.2731
95.504; 91.157; 101.221
888.78Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat
Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds
Organic Chemistry Frontiers, 2015, 2, 312
1553073 CIFC20 H18 N4 O2P -15.6257; 19.7469; 23.768
79.737; 88.28; 82.746
2577.3Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat
Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds
Organic Chemistry Frontiers, 2015, 2, 312
1553074 CIFC20 H13 N O4P -17.1728; 8.0196; 12.8455
84.142; 89.687; 87.901
734.56Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat
Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds
Organic Chemistry Frontiers, 2015, 2, 312
1553075 CIFC9 H9 N7 OP c a 219.9162; 14.8123; 7.3118
90; 90; 90
1073.97Quinodoz, Pierre; Lo, Cheikh; Kletskii, Mikhail; Burov, Oleg; Marrot, Jérôme; Couty, François
Regio- and stereoselective synthesis of α-hydroxy-β-azido tetrazoles
Organic Chemistry Frontiers, 2015, 2, 492
1553076 CIFC15 H13 N O5 SP 3210.3879; 10.3879; 24.218
90; 90; 120
2263.2Quan, Mao; Yang, Guoqiang; Xie, Fang; Gridnev, Ilya D.; Zhang, Wanbin
Pd(ii)-catalyzed asymmetric addition of arylboronic acids to cyclic N-sulfonyl ketimine esters and a DFT study of its mechanism
Organic Chemistry Frontiers, 2015, 2, 398
1553083 CIFC23 H21 B F10 N2P 1 21/c 119.6299; 19.4566; 12.265
90; 101.938; 90
4583.1Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553084 CIFC23 H18.711 B F10 N2P 1 21/n 111.5423; 12.863; 15.801
90; 93.409; 90
2341.8Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553085 CIFC29 H39 B N2P c c n16.756; 19.073; 15.93
90; 90; 90
5091Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553086 CIFC18 H25 B N2P 1 21 18.4021; 10.0498; 9.2882
90; 93.645; 90
782.7Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553087 CIFC13 H23 B N2P 1 21 19.2454; 7.0797; 9.5352
90; 100.812; 90
613.04Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553088 CIFC15 H27 B N2P 1 21/c 17.4085; 9.5348; 20.4481
90; 97.479; 90
1432.14Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553089 CIFC13 H21 B Cl2 N2P 1 21/n 18.8877; 14.4614; 10.8854
90; 91.815; 90
1398.38Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553090 CIFC37 H20 B2 Cl2 F20 N2P 1 c 110.6012; 10.7318; 16.8601
90; 105.327; 90
1849.9Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553091 CIFC11 H24 B PP 1 21/c 111.0408; 6.6868; 16.9825
90; 97.038; 90
1244.3Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553095 CIFC14 H16 O3P -19.017; 12.174; 12.8341
108.889; 99.634; 109.852
1191.34Dethe, Dattatraya H.; Boda, Raghavender; Murhade, Ganesh M.
Lewis acid catalyzed Nazarov type cyclization for the synthesis of a substituted indane framework: total synthesis of (±)-mutisianthol
Organic Chemistry Frontiers, 2015, 2, 645
1553096 CIFC56 H79 B5 O10P 21 21 2112.38928; 20.5595; 23.639
90; 90; 90
6021.26Da Ros, Sara; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Boronic esters of corannulene: potential building blocks toward icosahedral supramolecules
Organic Chemistry Frontiers, 2015, 2, 626
1553097 CIFC46 H46 B5 Cl3 O10P m n 2120.2644; 13.18215; 8.2499
90; 90; 90
2203.78Da Ros, Sara; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Boronic esters of corannulene: potential building blocks toward icosahedral supramolecules
Organic Chemistry Frontiers, 2015, 2, 626
1553098 CIFC32 H22 Cl2 SiP 1 21/c 19.959; 24.396; 11.0384
90; 108.602; 90
2541.8Xu, Liang; Zhang, Shuai; Li, Pengfei
Synthesis of silafluorenes and silaindenes via silyl radicals from arylhydrosilanes: intramolecular cyclization and intermolecular annulation with alkynes
Organic Chemistry Frontiers, 2015, 2, 459
1553099 CIFC25 H29 N O3P 21 21 215.572; 15.48; 25.4858
90; 90; 90
2198.3Arena, Giada; Cini, Elena; Petricci, Elena; Randino, Rosario; Taddei, Maurizio
A highly stereo-controlled protocol to prepare pipecolic acids based on Heck and cyclohydrocarbonylation reactions
Organic Chemistry Frontiers, 2015, 2, 526
1553100 CIFC23 H16 O3.19P 1 21/c 122.264; 10.1945; 30.92
90; 91.849; 90
7014Liu, Tong; Ding, Qiuping; Zong, Qianshou; Qiu, Guanyinsheng
Radical 5-exo cyclization of alkynoates with 2-oxoacetic acids for synthesis of 3-acylcoumarins
Organic Chemistry Frontiers, 2015, 2, 670
1553101 CIFC18 H13 N O2P -17.159; 9.364; 10.541
78.846; 82.356; 72.557
659.3Dethe, Dattatraya H.; Kumar B, Vijay
Concise asymmetric total synthesis of bruceolline J
Organic Chemistry Frontiers, 2015, 2, 548
1553102 CIFC30 H24 F12 N6 Ru Sb2P -3 c 110.786; 10.786; 17.286
90; 90; 120
1741.59Gomes, Filipe; Narbonne, Vanessa; Blanchard, Florent; Maestri, Giovanni; Malacria, Max
Formal base-free homolytic aromatic substitutions via photoredox catalysis
Organic Chemistry Frontiers, 2015, 2, 464
1553103 CIFC16 H22 N O3 SP -16.2097; 11.272; 11.547
104.782; 101.238; 100.235
744.1Zhang, Yan-Yan; Hao, Jian; Shi, Min
One pot cascade synthesis of fused heterocycles from furan-tethered terminal alkynes and aldehydes in the presence of amines and CuBr
Organic Chemistry Frontiers, 2015, 2, 394
1553104 CIFC16 H17 N O3 SP -18.3878; 9.8582; 19.139
76.354; 84.421; 73.985
1477.3Zhang, Yan-Yan; Hao, Jian; Shi, Min
One pot cascade synthesis of fused heterocycles from furan-tethered terminal alkynes and aldehydes in the presence of amines and CuBr
Organic Chemistry Frontiers, 2015, 2, 394
1553105 CIFC17 H19 N O3 SP 1 21/c 114.5933; 9.6858; 11.3977
90; 92.745; 90
1609.2Zhang, Yan-Yan; Hao, Jian; Shi, Min
One pot cascade synthesis of fused heterocycles from furan-tethered terminal alkynes and aldehydes in the presence of amines and CuBr
Organic Chemistry Frontiers, 2015, 2, 394
1553106 CIFC33 H30 Br N O5I 2 2 215.713; 28.08; 28.507
90; 90; 90
12578Zhang, Jun-Wei; Liu, Xiao-Wei; Gu, Qing; Shi, Xiao-Xin; You, Shu-Li
Enantioselective synthesis of 4,5,6,7-tetrahydroindoles via olefin cross-metathesis/intramolecular Friedel–Crafts alkylation reaction of pyrroles
Organic Chemistry Frontiers, 2015, 2, 476
1553107 CIFC17 H0 I2 N3 O6P 1 21/c 15.5881; 18.985; 10.6706
90; 94.113; 90
1129.13Zhang, Shuo; Chen, Ying; Wang, Jianwu; Pan, Yue; Xu, Zhenghu; Tung, Chen-Ho
An efficient synthesis of gem-diiodoolefins and (E)-iodoalkenes from propargylic amides with a Cu(i)/Cu(iii) cycle
Organic Chemistry Frontiers, 2015, 2, 578
1553108 CIFC23 H25 N O5P -19.2215; 10.9612; 11.6484
87.764; 69.092; 73.409
1051.48Zhang, Shuo; Chen, Ying; Wang, Jianwu; Pan, Yue; Xu, Zhenghu; Tung, Chen-Ho
An efficient synthesis of gem-diiodoolefins and (E)-iodoalkenes from propargylic amides with a Cu(i)/Cu(iii) cycle
Organic Chemistry Frontiers, 2015, 2, 578
1553109 CIFC23 H17 I O3C 1 2/c 126.291; 8.781; 18.363
90; 111.863; 90
3934Zhu, Hai-Tao; Fan, Ming-Jin; Yang, De-Suo; Wang, Xiao-Ling; Ke, Sen; Zhang, Chao-Yang; Guan, Zheng-Hui
An iodine-promoted Meyer–Schuster rearrangement for the synthesis of α-iodo unsaturated ketones
Organic Chemistry Frontiers, 2015, 2, 506
1553110 CIFC59 H49 Cl4 F6 N P3 RhP 1 21/c 112.3535; 28.8354; 15.2713
90; 99.472; 90
5365.7Chen, Shanshan; Su, Yan; Han, Keli; Li, Xingwei
Mechanistic studies on C‒C reductive coupling of five-coordinate Rh(iii) complexes
Organic Chemistry Frontiers, 2015, 2, 783
1553111 CIFC65 H61 F6 N O2 P3 RhP -110.8319; 13.2288; 22.0889
75.156; 79.856; 69.201
2847.44Chen, Shanshan; Su, Yan; Han, Keli; Li, Xingwei
Mechanistic studies on C–C reductive coupling of five-coordinate Rh(iii) complexes
Organic Chemistry Frontiers, 2015, 2, 783
1553112 CIFC59 H46 Cl2 F9 N P3 RhP 1 21/n 113.6534; 25.7008; 15.5862
90; 93.092; 90
5461.29Chen, Shanshan; Su, Yan; Han, Keli; Li, Xingwei
Mechanistic studies on C‒C reductive coupling of five-coordinate Rh(iii) complexes
Organic Chemistry Frontiers, 2015, 2, 783
1553113 CIFC58 H52 B Cl6 F4 N O Os P2P 1 21/n 116.5731; 19.6848; 18.1839
90; 112.182; 90
5493.2Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping
Reactions of osmapyridinium with terminal alkynes
Organic Chemistry Frontiers, 2015, 2, 560
1553114 CIFC56.25 H52.25 B Cl2.75 F4 N O3 Os P2P 1 21/c 111.9299; 14.1946; 33.0235
90; 98.576; 90
5529.7Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping
Reactions of osmapyridinium with terminal alkynes
Organic Chemistry Frontiers, 2015, 2, 560
1553115 CIFC50 H43 B Cl5 F4 N3 O Os PP 1 21/c 112.0746; 18.8448; 20.9677
90; 90.023; 90
4771.06Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping
Reactions of osmapyridinium with terminal alkynes
Organic Chemistry Frontiers, 2015, 2, 560
1553116 CIFC52 H55 B Cl4 F4 N3 Os PC 1 c 119.3445; 16.8974; 16.1902
90; 111.004; 90
4940.5Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping
Reactions of osmapyridinium with terminal alkynes
Organic Chemistry Frontiers, 2015, 2, 560
1553117 CIFC19 H21 N O3P 1 21/c 17.2941; 13.2249; 17.2264
90; 96.919; 90
1649.62Santos, Hugo; Distiller, Amy; D'Souza, Asha M.; Arnoux, Quentin; White, Jonathan M.; Meyer, Adam G.; Ryan, John H.
1,3-Dipolar cycloaddition reactions of phthalic anhydrides with an azomethine ylide
Organic Chemistry Frontiers, 2015, 2, 705
1553118 CIFC32 H37 N O4 S SnP 1 21 18.592; 10.956; 16.545
90; 92.673; 90
1556Kamimura, Akio; Yoshinaga, Tatsuro; Noguchi, Fumiaki; Miyazaki, Koichiro; Uno, Hidemitsu
A mechanistic study on the SHi reaction at tin atoms in a radical cascade reaction
Organic Chemistry Frontiers, 2015, 2, 713
1553119 CIFC16 H16 Cl I O SP 21 21 217.6495; 12.803; 16.9343
90; 90; 90
1658.5Berthelot-Bréhier, Anaïs; Panossian, Armen; Colobert, Françoise; Leroux, Frédéric R.
Atroposelective synthesis of axially chiral P,S-ligands based on arynes
Organic Chemistry Frontiers, 2015, 2, 634
1553120 CIFC28 H26 Cl P SP 21 21 219.4309; 13.5255; 19.3191
90; 90; 90
2464.3Berthelot-Bréhier, Anaïs; Panossian, Armen; Colobert, Françoise; Leroux, Frédéric R.
Atroposelective synthesis of axially chiral P,S-ligands based on arynes
Organic Chemistry Frontiers, 2015, 2, 634
1553121 CIFC35 H34 Cl3 P Pd SP 21 21 2111.8312; 15.3726; 17.795
90; 90; 90
3236.49Berthelot-Bréhier, Anaïs; Panossian, Armen; Colobert, Françoise; Leroux, Frédéric R.
Atroposelective synthesis of axially chiral P,S-ligands based on arynes
Organic Chemistry Frontiers, 2015, 2, 634
1553122 CIFC19 H20 F3 NP 1 21 110.4422; 33.2582; 10.4466
90; 114.77; 90
3294.2Chen, Mu-Wang; Ye, Zhi-Shi; Chen, Zhang-Pei; Wu, Bo; Zhou, Yong-Gui
Enantioselective synthesis of trifluoromethyl substituted piperidines with multiple stereogenic centers via hydrogenation of pyridinium hydrochlorides
Organic Chemistry Frontiers, 2015, 2, 586
1553123 CIFC23 H35 N S Si TiP 1 21/c 118.029; 9.695; 14.246
90; 110.517; 90
2332.1Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro
Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes
Organic Chemistry Frontiers, 2015, 2, 681
1553124 CIFC23 H35 N S Si ZrP 1 21/c 118.125; 9.87; 14.346
90; 110.563; 90
2402.9Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro
Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes
Organic Chemistry Frontiers, 2015, 2, 681
1553125 CIFC18 H25 N S Si ZrP 1 21/c 115.471; 9.164; 14.06
90; 108.282; 90
1892.8Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro
Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes
Organic Chemistry Frontiers, 2015, 2, 681
1553126 CIFC8 H17 N S SiP -16.2605; 6.9304; 14.4299
92.0278; 99.0665; 112.207
569.305Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro
Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes
Organic Chemistry Frontiers, 2015, 2, 681
1553127 CIFC18 H16 O2 SP 1 21/n 18.3022; 11.1608; 16.3992
90; 94.272; 90
1515.31Chen, Dianpeng; Xing, Gangdong; Zhou, Hongwei
Sulfone promoted Rh(iii)-catalyzed C–H activation and base assisted 1,5-H shift strategy for the construction of seven-membered rings
Organic Chemistry Frontiers, 2015, 2, 947
1553128 CIFC17 H21 N O3P -18.6808; 8.9707; 11.2873
104.818; 112.003; 92.742
777.67Liu, Xianglei; Gu, Zhenhua
Pd-catalyzed Heck cyclization and in situ hydrocarboxylation or hydromethenylation via a hydrogen borrowing strategy
Organic Chemistry Frontiers, 2015, 2, 778
1553129 CIFC16 H25 F O2P 21 21 215.9958; 13.644; 17.789
90; 90; 90
1455.3Zhang, Xiaofei; Guo, Shuo; Tang, Pingping
Transition-metal free oxidative aliphatic C–H fluorination
Organic Chemistry Frontiers, 2015, 2, 806
1553130 CIFC24 H31 F O8P 21 21 218.7359; 12.804; 20.625
90; 90; 90
2307Zhang, Xiaofei; Guo, Shuo; Tang, Pingping
Transition-metal free oxidative aliphatic C–H fluorination
Organic Chemistry Frontiers, 2015, 2, 806
1553131 CIFC16 H24 Cl2 N2 O PdP 1 21 112.1876; 9.8204; 15.854
90; 96.796; 90
1884.2Yu, Feng; Chen, Pinhong; Liu, Guosheng
Pd(ii)-catalyzed intermolecular enantioselective hydroamination of styrenes
Organic Chemistry Frontiers, 2015, 2, 819
1553132 CIFC13 H23 N O3 SP 1 21 110.291; 5.9808; 12.068
90; 103.531; 90
722.1Ye, Jian-Liang; Zhang, Yu-Feng; Liu, Yang; Zhang, Jin-Yuan; Ruan, Yuan-Ping; Huang, Pei-Qiang
Studies on the asymmetric synthesis of pandamarilactonines: an unexpected syn-selective vinylogous Mannich reaction of N-tert-butanesulfinimines
Organic Chemistry Frontiers, 2015, 2, 697
1553133 CIFC33 H36 N O8 P SP -110.3564; 12.0563; 14.1956
69.77; 82.139; 68.496
1547.3Kondoh, Azusa; Terada, Masahiro
Brønsted base-catalyzed α-oxygenation of carbonyl compounds utilizing the [1,2]-phospha-Brook rearrangement
Organic Chemistry Frontiers, 2015, 2, 801
1553134 CIFC11 H13 N O7 S2P 21 21 217.82043; 10.2265; 17.491
90; 90; 90
1398.85Kang, Jian; Zhu, Baofu; Liu, Jiewei; Wang, Bo; Zhang, Li; Su, Cheng-Yong
Chiral dirhodium catalysts derived from l-serine, l-threonine and l-cysteine: design, synthesis and application
Organic Chemistry Frontiers, 2015, 2, 890
1553135 CIFC11 H12 N2 O7 SP 4115.41418; 15.41418; 5.95145
90; 90; 90
1414.05Kang, Jian; Zhu, Baofu; Liu, Jiewei; Wang, Bo; Zhang, Li; Su, Cheng-Yong
Chiral dirhodium catalysts derived from l-serine, l-threonine and l-cysteine: design, synthesis and application
Organic Chemistry Frontiers, 2015, 2, 890
1553136 CIFC14 H14 N2 O3P 1 2/c 112.8276; 8.4882; 24.8068
90; 91.044; 90
2700.6Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie
Palladium-catalyzed direct ortho C‒O bond construction of azoxybenzenes with carboxylic acids and alcohols
Organic Chemistry Frontiers, 2015, 2, 951
1553137 CIFC28 H21 F3 N4 O6 Pd2P 1 21/c 114.4863; 17.2032; 11.5651
90; 105.969; 90
2770.93Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie
Palladium-catalyzed direct ortho C‒O bond construction of azoxybenzenes with carboxylic acids and alcohols
Organic Chemistry Frontiers, 2015, 2, 951
1553138 CIFC17 H18 N2 O3P -16.8879; 8.282; 14.4023
104.655; 94.121; 91.668
791.85Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie
Palladium-catalyzed direct ortho C–O bond construction of azoxybenzenes with carboxylic acids and alcohols
Organic Chemistry Frontiers, 2015, 2, 951
1553139 CIFC20 H26 N O2 SP -18.6248; 9.8158; 11.6537
99.05; 101.411; 96.596
944.1Pan, Dong; Chen, Gen-Qiang; Tang, Xiang-Ying; Shi, Min
Palladium-catalyzed intramolecular rearrangement of vinylidenecyclopropanes through C‒C bond activation
Organic Chemistry Frontiers, 2015, 2, 792
1553140 CIFC30 H31 N O2 SP 1 21/n 18.5768; 10.2978; 28.986
90; 90.183; 90
2560.1Pan, Dong; Chen, Gen-Qiang; Tang, Xiang-Ying; Shi, Min
Palladium-catalyzed intramolecular rearrangement of vinylidenecyclopropanes through C–C bond activation
Organic Chemistry Frontiers, 2015, 2, 792
1553141 CIFC21 H22 Br N3 O5P 1 21 19.8915; 9.4814; 11.942
90; 102.048; 90
1095.31Hu, Ying; Zhou, Zijun; Gong, Lei; Meggers, Eric
Asymmetric aza-Henry reaction to provide oxindoles with quaternary carbon stereocenter catalyzed by a metal-templated chiral Brønsted base
Organic Chemistry Frontiers, 2015, 2, 968
1553142 CIFC14 H15 Br N2 O3P n a 217.1573; 21.4898; 9.4975
90; 90; 90
1460.8Hu, Ying; Zhou, Zijun; Gong, Lei; Meggers, Eric
Asymmetric aza-Henry reaction to provide oxindoles with quaternary carbon stereocenter catalyzed by a metal-templated chiral Brønsted base
Organic Chemistry Frontiers, 2015, 2, 968
1553143 CIFC70 H66 Cl34 N8 P2 Ru2P 1 21/n 113.25; 16.9695; 23.3436
90; 103.948; 90
5093.95Mejuto, Carmen; García-Eleno, Marco A.; Guisado-Barrios, Gregorio; Spasyuk, Denis; Gusev, Dmitri; Peris, Eduardo
Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties
Organic Chemistry Frontiers, 2015, 2, 936
1553144 CIFC32 H35 Cl2 N4 O5 P RuP 1 21/c 118.2792; 11.74106; 17.1049
90; 117.389; 90
3259.49Mejuto, Carmen; García-Eleno, Marco A.; Guisado-Barrios, Gregorio; Spasyuk, Denis; Gusev, Dmitri; Peris, Eduardo
Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties
Organic Chemistry Frontiers, 2015, 2, 936
1553145 CIFC26 H17 O3 PP 21 21 218.4926; 12.013; 19.248
90; 90; 90
1963.7Xu, Guangqing; Li, Minghong; Wang, Shouliang; Tang, Wenjun
Efficient synthesis of P-chiral biaryl phosphonates by stereoselective intramolecular cyclization
Organic Chemistry Frontiers, 2015, 2, 1342
1553146 CIFC25 H23 Au I N3 OC 1 2/c 132.577; 10.964; 15.077
90; 101.267; 90
5281.3Xu, Qin; Gu, Peng; Wang, Feijun; Shi, Min
Selectfluor promoted NHC‒oxazoline gold(i) complex catalyzed cycloaddition/oxidation reaction of enynones with alkenes
Organic Chemistry Frontiers, 2015, 2, 1475
1553147 CIFC23 H19 Au I N3 OP 21 21 2110.3025; 16.0231; 26.3966
90; 90; 90
4357.5Xu, Qin; Gu, Peng; Wang, Feijun; Shi, Min
Selectfluor promoted NHC‒oxazoline gold(i) complex catalyzed cycloaddition/oxidation reaction of enynones with alkenes
Organic Chemistry Frontiers, 2015, 2, 1475
1553148 CIFC24 H34 O10P 21 21 215.8507; 14.177; 30.834
90; 90; 90
2557.5Huang, Xin; Xue, Can; Fu, Chunling; Ma, Shengming
A concise construction of carbohydrate-tethered axially chiral allenes via copper catalysis
Organic Chemistry Frontiers, 2015, 2, 1040
1553149 CIFC21 H19 N O6P 21 21 2110.8569; 14.913; 23.1808
90; 90; 90
3753.2Duan, Jindian; Cheng, Jing; Li, Pengfei
Enantioselective construction of spiro-1,3-indandiones with three stereocenters via organocatalytic Michael-aldol reaction of 2-arylideneindane-1,3-diones and nitro aldehydes
Organic Chemistry Frontiers, 2015, 2, 1048
1553150 CIFC72 H74 I2 N36 O16P n a 2113.093; 25.621; 27.14
90; 90; 90
9104Zhou, Tian-You; Qi, Qiao-Yan; Zhang, Ying; Xu, Xiao-Na; Zhao, Xin
A thermally stable pH-responsive “supramolecular buckle” based on the encapsulation of 4-(4-aminophenyl)-N-methylpyridinium by cucurbit[8]uril
Organic Chemistry Frontiers, 2015, 2, 1030
1553151 CIFC18 H19 N O2C 1 2/c 120.293; 6.84225; 22.5979
90; 90.8593; 90
3137.36Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553152 CIFC18 H19 N O2P 1 21/c 17.63367; 29.2305; 6.84862
90; 102.295; 90
1493.12Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553153 CIFC19 H21 N O2P b c a12.4972; 14.1613; 17.5538
90; 90; 90
3106.61Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553154 CIFC16 H17 N O3P 21 21 216.86998; 15.21957; 27.0563
90; 90; 90
2828.96Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553155 CIFC19 H21 N O3P -16.98428; 15.3845; 16.6168
110.497; 97.0023; 102.274
1596.16Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553156 CIFC18 H20 N2 O3P -16.8071; 15.0202; 15.8559
90.798; 101.156; 100.035
1564.3Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553157 CIFC11 H14 N2 O2P -17.5414; 11.8446; 12.2635
80.154; 88.093; 88.519
1078.48Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553158 CIFC46 H42 N2 OC 1 2/c 112.55604; 15.09459; 18.9643
90; 105.866; 90
3457.35Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553159 CIFC48 H46 N2 O3P -110.1705; 10.2903; 19.4528
99.778; 99.679; 106.888
1868.04Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553160 CIFC34 H34 N2 OP 1 21/c 111.9986; 10.6018; 20.9045
90; 104.851; 90
2570.36Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553161 CIFC15 H18 N2 O2P 1 21/n 118.06936; 17.802; 18.2203
90; 90.5295; 90
5860.69Huang, Pei-Qiang; Ou, Wei; Ye, Jian-Liang
Aza-Knoevenagel-type condensation of secondary amides: direct access to N-monosubstituted β,β-difunctionalized enamines
Organic Chemistry Frontiers, 2015, 2, 1094
1553162 CIFC10 H9 F3 O2 S2P 1 21/n 19.4647; 5.7312; 22.1678
90; 100.283; 90
1183.16Yang, Hai-Bin; Fan, Xing; Wei, Yin; Shi, Min
Solvent-controlled nucleophilic trifluoromethylthiolation of Morita–Baylis–Hillman carbonates: dual roles of DABCO in activating the Zard's trifluoromethylthiolation reagent and the MBH carbonates
Organic Chemistry Frontiers, 2015, 2, 1088
1553163 CIFC23 H27 N O3P 1 21/c 110.695; 21.389; 9.1312
90; 99.66; 90
2059.2Li, Ming; Qiu, Bin; Kong, Xiang-Jing; Wen, Li-Rong
Synthesis of Passerini adducts from aldehydes and isocyanides under the auxiliary of water
Organic Chemistry Frontiers, 2015, 2, 1326
1553164 CIFC22 H24 Cl N O4P b c a12.5003; 9.5999; 34.846
90; 90; 90
4181.6Li, Ming; Qiu, Bin; Kong, Xiang-Jing; Wen, Li-Rong
Synthesis of Passerini adducts from aldehydes and isocyanides under the auxiliary of water
Organic Chemistry Frontiers, 2015, 2, 1326
1553165 CIFC30 H23 N O2P -18.8044; 9.6097; 13.3333
93.346; 95.699; 90.433
1120.5Guo, Tenglong; Jiang, Quanbin; Yu, Zhengkun
Palladium-catalyzed oxidative annulation of in situ generated enones to pyrroles: a concise route to functionalized indoles
Organic Chemistry Frontiers, 2015, 2, 1361
1553166 CIFC10 H8 N4 OP b c a7.008; 13.515; 19.467
90; 90; 90
1843.8Li, Pan; Zhao, Jingjing; Xia, Chungu; Li, Fuwei
The development of carbene-stabilized N–O radical coupling strategy in metal-free regioselective C–H azidation of quinoline N-oxides
Organic Chemistry Frontiers, 2015, 2, 1313
1553167 CIFC25 H0 N24 O0.5P -110.974; 13.036; 14.337
68.085; 67.898; 73.316
1737Song, Chuanling; Sun, Yihua; Wang, Jianwu; Chen, Hui; Yao, Jiannian; Tung, Chen-Ho; Xu, Zhenghu
Successive Cu/Pd transmetalation relay catalysis in stereoselective synthesis of tetraarylethenes
Organic Chemistry Frontiers, 2015, 2, 1366
1553168 CIFC36 H40 O8C 1 2/c 18.621; 21.744; 18.379
90; 100.954; 90
3382.5Song, Chuanling; Sun, Yihua; Wang, Jianwu; Chen, Hui; Yao, Jiannian; Tung, Chen-Ho; Xu, Zhenghu
Successive Cu/Pd transmetalation relay catalysis in stereoselective synthesis of tetraarylethenes
Organic Chemistry Frontiers, 2015, 2, 1366
1553169 CIFC33 H41 N O9P 1 21/c 19.7518; 17.4971; 20.0458
90; 101.206; 90
3355.17Song, Chuanling; Sun, Yihua; Wang, Jianwu; Chen, Hui; Yao, Jiannian; Tung, Chen-Ho; Xu, Zhenghu
Successive Cu/Pd transmetalation relay catalysis in stereoselective synthesis of tetraarylethenes
Organic Chemistry Frontiers, 2015, 2, 1366
1553170 CIFC15 H14 O3 SP -18.503; 10.6762; 15.8607
76.75; 81.107; 88.437
1384.6Li, Siyu; Li, Xiang; Yang, Fan; Wu, Yangjie
Copper-catalyzed direct decarboxylative hydrosulfonylation of aryl propiolic acids with sulfonylhydrazides leading to vinylsulfones
Organic Chemistry Frontiers, 2015, 2, 1076
1553171 CIFC28 H29 N3 O4 S2P 1 21/n 110.2945; 18.1137; 14.6463
90; 105.831; 90
2627.5Zhang, Yong-Sheng; Tang, Xiang-Ying; Shi, Min
Divergent synthesis of indole-fused polycycles via Rh(ii)-catalyzed intramolecular [3 + 2] cycloaddition and C–H functionalization of indolyltriazoles
Organic Chemistry Frontiers, 2015, 2, 1516
1553172 CIFC27 H24 Cl3 N3 O4 S2P -111.3585; 11.981; 13.438
106.42; 108.985; 104.217
1539.6Zhang, Yong-Sheng; Tang, Xiang-Ying; Shi, Min
Divergent synthesis of indole-fused polycycles via Rh(ii)-catalyzed intramolecular [3 + 2] cycloaddition and C–H functionalization of indolyltriazoles
Organic Chemistry Frontiers, 2015, 2, 1516
1553173 CIFC26 H23 Cl F7 N OC 1 c 112.89225; 15.11065; 24.8076
90; 101.997; 90
4727.22Lao, Ye-Xing; Wu, Jia-Qiang; Chen, Yunyun; Zhang, Shang-Shi; Li, Qingjiang; Wang, Honggen
Palladium-catalyzed methylene C(sp3)–H arylation of the adamantyl scaffold
Organic Chemistry Frontiers, 2015, 2, 1374
1553174 CIFC9 H6 F3 N3P 1 21/c 111.6048; 11.0429; 22.106
90; 94.237; 90
2825.2Wang, Shuai; Yang, Li-Jun; Zeng, Jun-Liang; Zheng, Yan; Ma, Jun-An
Silver-catalyzed [3 + 2] cycloaddition of isocyanides with diazo compounds: new regioselective access to 1,4-disubstituted-1,2,3-triazoles
Organic Chemistry Frontiers, 2015, 2, 1468
1553175 CIFC11 H7 F6 N3P 1 21/c 110.63; 8.222; 13.645
90; 100.814; 90
1171.4Wang, Shuai; Yang, Li-Jun; Zeng, Jun-Liang; Zheng, Yan; Ma, Jun-An
Silver-catalyzed [3 + 2] cycloaddition of isocyanides with diazo compounds: new regioselective access to 1,4-disubstituted-1,2,3-triazoles
Organic Chemistry Frontiers, 2015, 2, 1468
1553176 CIFC23 H19 Cl O2C 1 2/c 128.386; 9.195; 17.591
90; 125.324; 90
3746.1Li, Yang; Liu, Bang; Ouyang, Xuan-Hui; Song, Ren-Jie; Li, Jin-Heng
Alkylation/1,2-aryl migration of α-aryl allylic alcohols with α-carbonyl alkyl bromides using visible-light photoredox catalysis
Organic Chemistry Frontiers, 2015, 2, 1457
1553177 CIFC25 H27 Br2 N5 O2P -18.8674; 9.3784; 16.618
82.99; 87.24; 62.65
1218.3Zende, V. M.; Schulzke, C.; Kapdi, A. R.
Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki–Miyaura arylation of bromoanthracene and related substrates
Organic Chemistry Frontiers, 2015, 2, 1397
1553178 CIFC21 H14 O2C 1 2/c 123.657; 7.2556; 18.859
90; 111.31; 90
3015.7Zende, V. M.; Schulzke, C.; Kapdi, A. R.
Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki–Miyaura arylation of bromoanthracene and related substrates
Organic Chemistry Frontiers, 2015, 2, 1397
1553179 CIFC26 H18P 1 21/n 110.441; 7.4965; 22.577
90; 94.06; 90
1762.7Zende, V. M.; Schulzke, C.; Kapdi, A. R.
Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki–Miyaura arylation of bromoanthracene and related substrates
Organic Chemistry Frontiers, 2015, 2, 1397
1553180 CIFC26 H18C 1 2/c 110.596; 13.501; 12.12
90; 90.38; 90
1733.8Zende, V. M.; Schulzke, C.; Kapdi, A. R.
Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki–Miyaura arylation of bromoanthracene and related substrates
Organic Chemistry Frontiers, 2015, 2, 1397
1553181 CIFC29 H27 N O4P -110.767; 11.483; 19.2866
88.719; 87.476; 80.292
2347.8Patra, Atanu; Bhunia, Anup; Yetra, Santhivardhana Reddy; Gonnade, Rajesh G.; Biju, Akkattu T.
Diastereoselective synthesis of cyclopentanone-fused spirooxindoles by N-heterocyclic carbene-catalyzed homoenolate annulation with isatilidenes
Organic Chemistry Frontiers, 2015, 2, 1584
1553183 CIFC21 H33 N O4 SiP 21 21 216.3258; 17.6205; 20.9213
90; 90; 90
2331.97Si, Chang-Mei; Mao, Zhuo-Ya; Liu, Yi-Wen; Du, Zhen-Ting; Wei, Bang-Guo; Lin, Guo-Qiang
Stereoselective formation of chiral trans-4-hydroxy-5-substituted 2-pyrrolidinones: syntheses of streptopyrrolidine and 3-epi-epohelmin A
Organic Chemistry Frontiers, 2015, 2, 1485
1553184 CIFC76 H19 N3 O5P 1 21/n 113.06; 13.2703; 29.7423
90; 95.06; 90
5134.6Xu, Liang; Liang, Sisi; Sun, Jiahao; Gan, Liangbing
Open-cage fullerene with a stopper acts as a molecular vial for a single water molecule
Organic Chemistry Frontiers, 2015, 2, 1500
1553185 CIFC82 H27 N5 O5P 1 21/c 117.987; 18.451; 19.171
90; 117.87; 90
5624Xu, Liang; Liang, Sisi; Sun, Jiahao; Gan, Liangbing
Open-cage fullerene with a stopper acts as a molecular vial for a single water molecule
Organic Chemistry Frontiers, 2015, 2, 1500
1553186 CIFC16 H8 Br F3 O2 SP 1 21/n 112.9202; 7.9412; 14.2105
90; 91.2584; 90
1457.67Zeng, Yao-Fu; Tan, Dong-Hang; Chen, Yunyun; Lv, Wen-Xin; Liu, Xu-Ge; Li, Qingjiang; Wang, Honggen
Direct radical trifluoromethylthiolation and thiocyanation of aryl alkynoate esters: mild and facile synthesis of 3-trifluoromethylthiolated and 3-thiocyanated coumarins
Organic Chemistry Frontiers, 2015, 2, 1511
1553187 CIFC22 H16 N2 OP 1 21/c 18.4582; 11.1421; 18.5214
90; 100.439; 90
1716.61Li, Yaxuan; Fu, Yajie; Ren, Chaojie; Tang, Dong; Wu, Ping; Meng, Xu; Chen, Baohua
Copper-catalyzed oxidative coupling reaction of α,β-unsaturated aldehydes with amidines: synthesis of 1,2,4-trisubstituted-1H-imidazole-5-carbaldehydes
Organic Chemistry Frontiers, 2015, 2, 1632
1553188 CIFC26 H23 F6 N2 O P2 RhP 1 21/c 110.6439; 11.6245; 21.782
90; 100.416; 90
2650.7Tang, Z.; Mandal, S.; Paul, N. D.; Lutz, M.; Li, P.; van der Vlugt, J. I.; de Bruin, B.
Rhodium catalysed conversion of carbenes into ketenes and ketene imines using PNN pincer complexes
Organic Chemistry Frontiers, 2015, 2, 1561
1553189 CIFC20 H27 F6 N2 O P2 RhP 1 21/n 113.4021; 10.9937; 15.6906
90; 97.462; 90
2292.3Tang, Z.; Mandal, S.; Paul, N. D.; Lutz, M.; Li, P.; van der Vlugt, J. I.; de Bruin, B.
Rhodium catalysed conversion of carbenes into ketenes and ketene imines using PNN pincer complexes
Organic Chemistry Frontiers, 2015, 2, 1561
1553190 CIFC22 H25 F6 N2 O2 P2 RhP -19.70447; 9.77001; 14.1603
83.358; 74.636; 74.636
1246.84Tang, Z.; Mandal, S.; Paul, N. D.; Lutz, M.; Li, P.; van der Vlugt, J. I.; de Bruin, B.
Rhodium catalysed conversion of carbenes into ketenes and ketene imines using PNN pincer complexes
Organic Chemistry Frontiers, 2015, 2, 1561
1553191 CIFC24 H25 Cl N2 O0.25 Ru SP -110.0366; 10.6641; 12.3895
70.891; 84.601; 64.031
1124.59Xie, Xiaoke; Huynh, Han Vinh
Cyclometallated ruthenium(ii) complexes with ditopic thienyl‒NHC ligands: syntheses and alkyne annulations
Organic Chemistry Frontiers, 2015, 2, 1598
1553192 CIFC30 H29 Cl N2 Ru SP 1 21/c 110.4555; 15.1572; 16.4668
90; 94.422; 90
2601.83Xie, Xiaoke; Huynh, Han Vinh
Cyclometallated ruthenium(ii) complexes with ditopic thienyl‒NHC ligands: syntheses and alkyne annulations
Organic Chemistry Frontiers, 2015, 2, 1598
1553193 CIFC24 H25 Br N2 Ru SP -110.5184; 10.8146; 11.5002
87.04; 64.781; 69.987
1105.18Xie, Xiaoke; Huynh, Han Vinh
Cyclometallated ruthenium(ii) complexes with ditopic thienyl‒NHC ligands: syntheses and alkyne annulations
Organic Chemistry Frontiers, 2015, 2, 1598
1553194 CIFC28 H27 Cl N2 Ru SP 1 21/n 114.301; 11.104; 15.932
90; 108.464; 90
2399.7Xie, Xiaoke; Huynh, Han Vinh
Cyclometallated ruthenium(ii) complexes with ditopic thienyl‒NHC ligands: syntheses and alkyne annulations
Organic Chemistry Frontiers, 2015, 2, 1598
1553244 CIFC37 H28 OP 1 21/c 111.6881; 17.6933; 12.7663
90; 97.516; 90
2617.4Hoang, Giang T.; Kubo, Tomohiro; Young, Victor G.; Kautzky, Jacob A.; Wissinger, Jane E.
Illustrating the Utility of X-ray Crystallography for Structure Elucidation through a Tandem Aldol Condensation/Diels–Alder Reaction Sequence
Journal of Chemical Education, 2015, 92, 1381
1553245 CIFC37 H28 OP -110.6896; 11.5817; 12.2608
118.181; 94.775; 99.292
1298.1Hoang, Giang T.; Kubo, Tomohiro; Young, Victor G.; Kautzky, Jacob A.; Wissinger, Jane E.
Illustrating the Utility of X-ray Crystallography for Structure Elucidation through a Tandem Aldol Condensation/Diels–Alder Reaction Sequence
Journal of Chemical Education, 2015, 92, 1381
1553249 CIFC21 H24 O5P 21 21 214.9653; 10.6228; 34.2129
90; 90; 90
1804.57Jiang, Junhang; Zheng, Canhui; Zhu, Kongkai; Liu, Jia; Sun, Nannan; Wang, Chongqing; Jiang, Hualiang; Zhu, Ju; Luo, Cheng; Zhou, Youjun
Quantum chemistry calculation-aided structural optimization of combretastatin A-4-like tubulin polymerization inhibitors: improved stability and biological activity.
Journal of medicinal chemistry, 2015, 58, 2538-2546
1553280 CIFC34 H54 O4P 21 21 219.3781; 12.6568; 27.0482
90; 90; 90
3210.53Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553281 CIFC69 H92 O13C 1 2 118.0066; 13.5854; 13.2739
90; 93.898; 90
3239.64Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553282 CIFC36 H54 O5P 1 21 19.3216; 13.2025; 13.8291
90; 107.968; 90
1618.92Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553283 CIFC30 H36 O4P 1 21 110.7509; 7.7655; 14.8907
90; 99.69; 90
1225.43Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553284 CIFC30 H44 O5P 21 21 2110.0575; 16.0634; 17.39
90; 90; 90
2809.49Yang, Xing-Wei; Li, Ming-Ming; Liu, Xia; Ferreira, Daneel; Ding, Yuanqing; Zhang, Jing-Jing; Liao, Yang; Qin, Hong-Bo; Xu, Gang
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi.
Journal of natural products, 2015, 78, 885-895
1553285 CIFC16 H24.6667 N2 O1.3333P 21 21 219.7135; 13.9213; 31.7069
90; 90; 90
4287.6Cao, Ming-Ming; Zhang, Yu; Huang, Sheng-Dian; Di, Ying-Tong; Peng, Zong-Gen; Jiang, Jian-Dong; Yuan, Chun-Mao; Chen, Duo-Zhi; Li, Shun-Lin; He, Hong-Ping; Hao, Xiao-Jiang
Alkaloids with Different Carbon Units from Myrioneuron faberi.
Journal of natural products, 2015, 78, 2609-2616
1553286 CIFC15 H26 N2P 1 21 19.1535; 5.1702; 14.568
90; 106.495; 90
661.06Cao, Ming-Ming; Zhang, Yu; Huang, Sheng-Dian; Di, Ying-Tong; Peng, Zong-Gen; Jiang, Jian-Dong; Yuan, Chun-Mao; Chen, Duo-Zhi; Li, Shun-Lin; He, Hong-Ping; Hao, Xiao-Jiang
Alkaloids with Different Carbon Units from Myrioneuron faberi.
Journal of natural products, 2015, 78, 2609-2616
1553287 CIFC15 H24 N2 OP -18.8466; 9.1188; 9.5971
95.094; 112.717; 112.004
636.97Cao, Ming-Ming; Zhang, Yu; Huang, Sheng-Dian; Di, Ying-Tong; Peng, Zong-Gen; Jiang, Jian-Dong; Yuan, Chun-Mao; Chen, Duo-Zhi; Li, Shun-Lin; He, Hong-Ping; Hao, Xiao-Jiang
Alkaloids with Different Carbon Units from Myrioneuron faberi.
Journal of natural products, 2015, 78, 2609-2616
1553992 CIFC16 H19 I N4 O4P -17.0211; 8.3237; 15.1967
86.651; 85.306; 89.485
883.62Rosokha, Sergiy V.; Loboda, Eric A.
Interplay of Halogen and π-π Charge-Transfer Bondings in Intermolecular Associates of Bromo- or Iododinitrobenzene with Tetramethyl-p-phenylenediamine.
The journal of physical chemistry. A, 2015, 119, 3833-3842
1553993 CIFC16 H19 Br N4 O4P -16.9478; 8.2799; 15.0522
94.6594; 93.2402; 90.2781
861.63Rosokha, Sergiy V.; Loboda, Eric A.
Interplay of Halogen and π-π Charge-Transfer Bondings in Intermolecular Associates of Bromo- or Iododinitrobenzene with Tetramethyl-p-phenylenediamine.
The journal of physical chemistry. A, 2015, 119, 3833-3842
1553994 CIFC18 H18 B Cl N2 O3P 1 21/n 17.7528; 19.1764; 11.3962
90; 93.209; 90
1691.63Golub, Igor E.; Gulyaeva, Ekaterina S.; Filippov, Oleg A.; Dyadchenko, Victor P.; Belkova, Natalia V.; Epstein, Lina M.; Arkhipov, Dmitry E.; Shubina, Elena S.
Dihydrogen bond intermediated alcoholysis of dimethylamine-borane in nonaqueous media.
The journal of physical chemistry. A, 2015, 119, 3853-3868
1553995 CIFC10 H16 B F12 N O4P 1 21/n 19.4694; 13.2943; 14.0325
90; 90.038; 90
1766.5Golub, Igor E.; Gulyaeva, Ekaterina S.; Filippov, Oleg A.; Dyadchenko, Victor P.; Belkova, Natalia V.; Epstein, Lina M.; Arkhipov, Dmitry E.; Shubina, Elena S.
Dihydrogen bond intermediated alcoholysis of dimethylamine-borane in nonaqueous media.
The journal of physical chemistry. A, 2015, 119, 3853-3868
1553996 CIFC12 H25.95 Cd N6 O8.98P 1 21/c 112.1161; 29.0903; 11.0501
90; 92.127; 90
3892Colaneri, Michael J.; Teat, Simon J.; Vitali, Jacqueline
Models for Copper Dynamic Behavior in Doped Cadmium dl-Histidine Crystals: Electron Paramagnetic Resonance and Crystallographic Analysis.
The journal of physical chemistry. A, 2015, 119, 11119-11127
1553997 CIFC12 H25.8 Cd N6 O8.9P 1 21/c 112.2555; 29.4689; 11.1087
90; 92.396; 90
4008.5Colaneri, Michael J.; Teat, Simon J.; Vitali, Jacqueline
Models for Copper Dynamic Behavior in Doped Cadmium dl-Histidine Crystals: Electron Paramagnetic Resonance and Crystallographic Analysis.
The journal of physical chemistry. A, 2015, 119, 11119-11127
1553998 CIFC29 H21 Cl NP -19.9486; 10.079; 10.8072
100.318; 90.072; 96.899
1058.1Pati, Avik Kumar; Gharpure, Santosh J.; Mishra, Ashok K.
Contrasting Solid-State Fluorescence of Diynes with Small and Large Aryl Substituents: Crystal Packing Dependence and Stimuli-Responsive Fluorescence Switching.
The journal of physical chemistry. A, 2015, 119, 10481-10493
1553999 CIFC18 H14 O2P 1 21/c 17.2042; 15.6697; 12.5803
90; 91.753; 90
1419.5Pati, Avik Kumar; Gharpure, Santosh J.; Mishra, Ashok K.
Contrasting Solid-State Fluorescence of Diynes with Small and Large Aryl Substituents: Crystal Packing Dependence and Stimuli-Responsive Fluorescence Switching.
The journal of physical chemistry. A, 2015, 119, 10481-10493
1554000 CIFC18 H15 NP 1 21/c 19.872; 12.082; 12.46
90; 103.028; 90
1447.9Pati, Avik Kumar; Gharpure, Santosh J.; Mishra, Ashok K.
Contrasting Solid-State Fluorescence of Diynes with Small and Large Aryl Substituents: Crystal Packing Dependence and Stimuli-Responsive Fluorescence Switching.
The journal of physical chemistry. A, 2015, 119, 10481-10493
1554001 CIFC17 H12 OP 1 21/c 113.8324; 9.3533; 10.2395
90; 101.943; 90
1296.1Pati, Avik Kumar; Gharpure, Santosh J.; Mishra, Ashok K.
Contrasting Solid-State Fluorescence of Diynes with Small and Large Aryl Substituents: Crystal Packing Dependence and Stimuli-Responsive Fluorescence Switching.
The journal of physical chemistry. A, 2015, 119, 10481-10493
1554002 CIFC16 H24 N5 OP 1 21/n 15.89; 14.574; 19.326
90; 93.463; 90
1655.9Haller, Benjamin C.; Chambers, Dallas; Cheng, Ran; Chemistruck, Victoria; Hom, Timothy F.; Li, Zhengzheng; Nguyen, Jeffrey; Ichimura, Andrew; Brook, David J. R.
Oxidation of Electron Donor-Substituted Verdazyls: Building Blocks for Molecular Switches.
The journal of physical chemistry. A, 2015, 119, 10750-10760
1554003 CIFC17 H25 F3 N5 O4 SP 1 21/c 116.865; 13.1791; 19.9462
90; 90.015; 90
4433.35Haller, Benjamin C.; Chambers, Dallas; Cheng, Ran; Chemistruck, Victoria; Hom, Timothy F.; Li, Zhengzheng; Nguyen, Jeffrey; Ichimura, Andrew; Brook, David J. R.
Oxidation of Electron Donor-Substituted Verdazyls: Building Blocks for Molecular Switches.
The journal of physical chemistry. A, 2015, 119, 10750-10760
1554004 CIFC16 H24 N5 OP 1 21 18.054; 5.95; 17.507
90; 95.31; 90
835.4Haller, Benjamin C.; Chambers, Dallas; Cheng, Ran; Chemistruck, Victoria; Hom, Timothy F.; Li, Zhengzheng; Nguyen, Jeffrey; Ichimura, Andrew; Brook, David J. R.
Oxidation of Electron Donor-Substituted Verdazyls: Building Blocks for Molecular Switches.
The journal of physical chemistry. A, 2015, 119, 10750-10760
1554031 CIFC26 H22 N OP 1 21/n 111.6367; 27.4387; 11.7856
90; 95.372; 90
3746.6Dyar, Scott M.; Margulies, Eric A.; Horwitz, Noah E.; Brown, Kristen E.; Krzyaniak, Matthew D.; Wasielewski, Michael R.
Photogenerated Quartet State Formation in a Compact Ring-Fused Perylene-Nitroxide.
The journal of physical chemistry. B, 2015, 119, 13560-13569
1554032 CIFC24 H26 N O5P -19.6761; 10.502; 10.8995
76.6369; 80.4476; 76.735
1041.37Ravat, Prince; Baumgarten, Martin
Positional Isomers of Tetramethoxypyrene-based Mono- and Biradicals.
The journal of physical chemistry. B, 2015, 119, 13649-13655
1554033 CIFC24 H26 N O5P 1 21/c 18.1986; 21.6402; 11.6933
90; 100.589; 90
2039.29Ravat, Prince; Baumgarten, Martin
Positional Isomers of Tetramethoxypyrene-based Mono- and Biradicals.
The journal of physical chemistry. B, 2015, 119, 13649-13655
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
1554035 CIFC6 Br2 N4 O4 SP -19.167; 10.2561; 11.4773
86.709; 77.084; 76.289
1021.78Pavan, 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
1554036 CIFC11 H5 N2 O5 aP c a 2132.1; 4.1188; 9.6966
90; 90; 90
1282.02Manin, Alex N.; Voronin, Alexander P.; Shishkina, Anastasia V.; Vener, Mikhail V.; Churakov, Andrei V.; Perlovich, German L.
Influence of Secondary Interactions on the Structure, Sublimation Thermodynamics, and Solubility of Salicylate:4-Hydroxybenzamide Cocrystals. Combined Experimental and Theoretical Study.
The journal of physical chemistry. B, 2015, 119, 10466-10477
1554037 CIFC14 H13 N O5P 1 21/c 113.8869; 8.01874; 12.8184
90; 115.187; 90
1291.69Manin, Alex N.; Voronin, Alexander P.; Shishkina, Anastasia V.; Vener, Mikhail V.; Churakov, Andrei V.; Perlovich, German L.
Influence of Secondary Interactions on the Structure, Sublimation Thermodynamics, and Solubility of Salicylate:4-Hydroxybenzamide Cocrystals. Combined Experimental and Theoretical Study.
The journal of physical chemistry. B, 2015, 119, 10466-10477
1554038 CIFC4 H6 O2P 1 21/n 13.614; 16.42; 6.773
90; 90.36; 90
401.9Marshall, William G.; Urquhart, Andrew J.; Oswald, Iain D. H.
Investigation of Methacrylic Acid at High Pressure Using Neutron Diffraction.
The journal of physical chemistry. B, 2015, 119, 12147-12154
1554039 CIFC56 H50 Co N6 O7P -116.652; 17.462; 22.655
90.18; 108.31; 116.32
5527Liu, Qiuhua; Zhang, Xi; Zeng, Wennan; Wang, Jianxiu; Zhou, Zaichun
Fine-Tuning of Electronic Structure of Cobalt(II) Ion in Nonplanar Porphyrins and Tracking of a Cross-Hybrid Stage: Implications for the Distortion of Natural Tetrapyrrole Macrocycles.
The journal of physical chemistry. B, 2015, 119, 14102-14110
1554040 CIFC59 H56 Co N6 O7P -115.633; 16.027; 16.146
61.61; 63.25; 63.09
3027.9Liu, Qiuhua; Zhang, Xi; Zeng, Wennan; Wang, Jianxiu; Zhou, Zaichun
Fine-Tuning of Electronic Structure of Cobalt(II) Ion in Nonplanar Porphyrins and Tracking of a Cross-Hybrid Stage: Implications for the Distortion of Natural Tetrapyrrole Macrocycles.
The journal of physical chemistry. B, 2015, 119, 14102-14110
1554041 CIFC58 H54 Co N6 O7P -114.149; 16.352; 16.598
60.98; 85.09; 65.72
3029.6Liu, Qiuhua; Zhang, Xi; Zeng, Wennan; Wang, Jianxiu; Zhou, Zaichun
Fine-Tuning of Electronic Structure of Cobalt(II) Ion in Nonplanar Porphyrins and Tracking of a Cross-Hybrid Stage: Implications for the Distortion of Natural Tetrapyrrole Macrocycles.
The journal of physical chemistry. B, 2015, 119, 14102-14110
1554042 CIFC57 H49 Cl3 Co N6 O6P -118.9824; 21.2118; 28.7759
73.804; 74.979; 67.777
10145.2Liu, Qiuhua; Zhang, Xi; Zeng, Wennan; Wang, Jianxiu; Zhou, Zaichun
Fine-Tuning of Electronic Structure of Cobalt(II) Ion in Nonplanar Porphyrins and Tracking of a Cross-Hybrid Stage: Implications for the Distortion of Natural Tetrapyrrole Macrocycles.
The journal of physical chemistry. B, 2015, 119, 14102-14110
1554053 CIFC20 H17 N O2P 1 21/c 110.194; 11.472; 13.683
90; 97.76; 90
1585.5Hariharan, P. S.; Venkataramanan, N. S.; Moon, Dohyun; Anthony, Savarimuthu Philip
Self-Reversible Mechanochromism and Thermochromism of a Triphenylamine-Based Molecule: Tunable Fluorescence and Nanofabrication Studies
The Journal of Physical Chemistry C, 2015, 119, 9460
1554054 CIFC8 H18 F6 Li O4 PP 1 21/n 16.1967; 12.558; 18.169
90; 95.745; 90
1406.8Han, Sang-Don; Yun, Sung-Hyun; Borodin, Oleg; Seo, Daniel M.; Sommer, Roger D.; Young, Victor G.; Henderson, Wesley A.
Solvate Structures and Computational/Spectroscopic Characterization of LiPF6 Electrolytes
The Journal of Physical Chemistry C, 2015, 119, 8492
1554055 CIFC5 H10 F3 Li0.5 O3 P0.5P n m a9.5125; 21.8997; 8.5903
90; 90; 90
1789.5Han, Sang-Don; Yun, Sung-Hyun; Borodin, Oleg; Seo, Daniel M.; Sommer, Roger D.; Young, Victor G.; Henderson, Wesley A.
Solvate Structures and Computational/Spectroscopic Characterization of LiPF6 Electrolytes
The Journal of Physical Chemistry C, 2015, 119, 8492
1554056 CIFC60 H80 N2 O4P -19.93781; 15.1528; 17.8125
69.7564; 88.9555; 87.1772
2513.57Kotwica, Kamil; Bujak, Piotr; Wamil, Damian; Pieczonka, Adam; Wiosna-Salyga, Gabriela; Gunka, Piotr A.; Jaroch, Tomasz; Nowakowski, Robert; Luszczynska, Beata; Witkowska, Ewelina; Glowacki, Ireneusz; Ulanski, Jacek; Zagorska, Malgorzata; Pron, Adam
Structural, Spectroscopic, Electrochemical, and Electroluminescent Properties of Tetraalkoxydinaphthophenazines: New Solution-Processable Nonlinear Azaacenes
The Journal of Physical Chemistry C, 2015, 119, 10700
1554057 CIFC68 H96 N2 O4P -19.8574; 17.6322; 17.7861
68.547; 87.477; 89.776
2874.1Kotwica, Kamil; Bujak, Piotr; Wamil, Damian; Pieczonka, Adam; Wiosna-Salyga, Gabriela; Gunka, Piotr A.; Jaroch, Tomasz; Nowakowski, Robert; Luszczynska, Beata; Witkowska, Ewelina; Glowacki, Ireneusz; Ulanski, Jacek; Zagorska, Malgorzata; Pron, Adam
Structural, Spectroscopic, Electrochemical, and Electroluminescent Properties of Tetraalkoxydinaphthophenazines: New Solution-Processable Nonlinear Azaacenes
The Journal of Physical Chemistry C, 2015, 119, 10700
1554058 CIFC12 H18 N4 OF d d 212.663; 33.528; 12.2027
90; 90; 90
5180.8Jeeva, Mani; Prabhu, G. Venkatesa; Boobalan, Maria susai; Rajesh, Chinnaiyan Mahalingam
Interactions and Inhibition Effect of Urea-Derived Mannich Bases on a Mild Steel Surface in HCl
The Journal of Physical Chemistry C, 2015, 119, 22025
1554059 CIFC11 H16 N4 O2F d d 212.2079; 34.449; 11.8236
90; 90; 90
4972.4Jeeva, Mani; Prabhu, G. Venkatesa; Boobalan, Maria susai; Rajesh, Chinnaiyan Mahalingam
Interactions and Inhibition Effect of Urea-Derived Mannich Bases on a Mild Steel Surface in HCl
The Journal of Physical Chemistry C, 2015, 119, 22025
1554060 CIFC25 H13 F6 I6 O PP 1 21/n 18.4758; 44.7106; 9.2023
90; 115.97; 90
3135.15Xu, Yijue; Viger-Gravel, Jasmine; Korobkov, Ilia; Bryce, David L.
Mechanochemical Production of Halogen-Bonded Solids Featuring P═O···I–C Motifs and Characterization via X-ray Diffraction, Solid-State Multinuclear Magnetic Resonance, and Density Functional Theory
The Journal of Physical Chemistry C, 2015, 119, 27104
1554061 CIFC30 H15 F8 I4 O PP -18.6823; 12.8395; 15.127
90.4885; 97.5416; 105.886
1606.12Xu, Yijue; Viger-Gravel, Jasmine; Korobkov, Ilia; Bryce, David L.
Mechanochemical Production of Halogen-Bonded Solids Featuring P═O···I‒C Motifs and Characterization via X-ray Diffraction, Solid-State Multinuclear Magnetic Resonance, and Density Functional Theory
The Journal of Physical Chemistry C, 2015, 119, 27104
1554062 CIFC24 H15 F3 I3 O PP -19.7436; 10.7585; 13.5453
113.174; 96.9048; 107.42
1198.74Xu, Yijue; Viger-Gravel, Jasmine; Korobkov, Ilia; Bryce, David L.
Mechanochemical Production of Halogen-Bonded Solids Featuring P═O···I–C Motifs and Characterization via X-ray Diffraction, Solid-State Multinuclear Magnetic Resonance, and Density Functional Theory
The Journal of Physical Chemistry C, 2015, 119, 27104
1554063 CIFC21 H16 F4 I2 N O PP n m a21.9816; 18.0739; 5.8075
90; 90; 90
2307.3Xu, Yijue; Viger-Gravel, Jasmine; Korobkov, Ilia; Bryce, David L.
Mechanochemical Production of Halogen-Bonded Solids Featuring P═O···I‒C Motifs and Characterization via X-ray Diffraction, Solid-State Multinuclear Magnetic Resonance, and Density Functional Theory
The Journal of Physical Chemistry C, 2015, 119, 27104
1554064 CIFC30 H15 F8 I4 O PP 1 21/c 19.319; 25.4268; 13.8063
90; 103.942; 90
3175.1Xu, Yijue; Viger-Gravel, Jasmine; Korobkov, Ilia; Bryce, David L.
Mechanochemical Production of Halogen-Bonded Solids Featuring P═O···I–C Motifs and Characterization via X-ray Diffraction, Solid-State Multinuclear Magnetic Resonance, and Density Functional Theory
The Journal of Physical Chemistry C, 2015, 119, 27104
1554147 CIFC28 H47 Lu O Si3P 1 21/c 110.4; 15.6; 20
90; 105; 90
3134.2Du, Gaixia; Long, Yingyun; Xue, Jiaping; Zhang, Shaowen; Dong, Yuping; Li, Xiaofang
1,4-Selective Polymerization of 1,3-Cyclohexadiene and Copolymerization with Styrene by Cationic Half-Sandwich Fluorenyl Rare Earth Metal Alkyl Catalysts
Macromolecules, 2015, 48, 1627
1554148 CIFC28 H47 O Si3 YP 1 21/c 110.4; 15.8; 20
90; 104.6; 90
3180.3Du, Gaixia; Long, Yingyun; Xue, Jiaping; Zhang, Shaowen; Dong, Yuping; Li, Xiaofang
1,4-Selective Polymerization of 1,3-Cyclohexadiene and Copolymerization with Styrene by Cationic Half-Sandwich Fluorenyl Rare Earth Metal Alkyl Catalysts
Macromolecules, 2015, 48, 1627
1554149 CIFC46 H38 O8P -15.8035; 12.8761; 13.1702
66.778; 82.336; 86.696
896.34Wang, Zhihan; Randazzo, Katelyn; Hou, Xiaodong; Simpson, Jeffrey; Struppe, Jochem; Ugrinov, Angel; Kastern, Brent; Wysocki, Erin; Chu, Qianli R.
Stereoregular Two-Dimensional Polymers Constructed by Topochemical Polymerization
Macromolecules, 2015, 48, 2894
1554150 CIFC18 H14 O4C 1 2/c 115.7822; 5.6013; 16.275
90; 99.255; 90
1419.99Wang, Zhihan; Randazzo, Katelyn; Hou, Xiaodong; Simpson, Jeffrey; Struppe, Jochem; Ugrinov, Angel; Kastern, Brent; Wysocki, Erin; Chu, Qianli R.
Stereoregular Two-Dimensional Polymers Constructed by Topochemical Polymerization
Macromolecules, 2015, 48, 2894
1554151 CIFC44 H68 N8 O10P 1 21/n 19.226; 20.5019; 24.273
90; 96.132; 90
4565Wang, Zhihan; Randazzo, Katelyn; Hou, Xiaodong; Simpson, Jeffrey; Struppe, Jochem; Ugrinov, Angel; Kastern, Brent; Wysocki, Erin; Chu, Qianli R.
Stereoregular Two-Dimensional Polymers Constructed by Topochemical Polymerization
Macromolecules, 2015, 48, 2894
1554152 CIFC23 H19 O4P 1 21/n 15.5677; 9.2109; 35.394
90; 91.726; 90
1814.3Wang, Zhihan; Randazzo, Katelyn; Hou, Xiaodong; Simpson, Jeffrey; Struppe, Jochem; Ugrinov, Angel; Kastern, Brent; Wysocki, Erin; Chu, Qianli R.
Stereoregular Two-Dimensional Polymers Constructed by Topochemical Polymerization
Macromolecules, 2015, 48, 2894
1554153 CIFC54 H46 O8P -15.8334; 14.4688; 14.48
119.601; 90.053; 95.149
1056.9Wang, Zhihan; Randazzo, Katelyn; Hou, Xiaodong; Simpson, Jeffrey; Struppe, Jochem; Ugrinov, Angel; Kastern, Brent; Wysocki, Erin; Chu, Qianli R.
Stereoregular Two-Dimensional Polymers Constructed by Topochemical Polymerization
Macromolecules, 2015, 48, 2894
1554154 CIFC8 H7 N O4C 1 2/c 112.6313; 7.672; 16.025
90; 107.02; 90
1484.9Kriechbaum, Konstantin; Cerrón-Infantes, D. Alonso; Stöger, Berthold; Unterlass, Miriam M.
Shape-Anisotropic Polyimide Particles by Solid-State Polycondensation of Monomer Salt Single Crystals
Macromolecules, 2015, 48, 8773
1554155 CIFC38 H38 N4 O4P 1 21/c 116.966; 10.138; 19.461
90; 104.447; 90
3241.5Lee, Young-Gi; Kang, Songsu; Moerdyk, Jonathan P.; Bielawski, Christopher W.
Poly(2-imino-4-oxazolidinone)s via the Condensation of Diamidocarbenes with Bis(isocyanate)s
Macromolecules, 2015, 48, 9081
1554156 CIFC31 H33 N3 O3P 1 21/n 117.244; 18.378; 19.472
90; 113.868; 90
5643.1Lee, Young-Gi; Kang, Songsu; Moerdyk, Jonathan P.; Bielawski, Christopher W.
Poly(2-imino-4-oxazolidinone)s via the Condensation of Diamidocarbenes with Bis(isocyanate)s
Macromolecules, 2015, 48, 9081
1554159 CIFC6 H7 K O8 S2P 1 21/n 17.3917; 5.808; 26.6182
90; 94.1545; 90
1139.74Potzmann, Paul Michael; Lopez Villanueva, Francisco Javier; Liska, Robert
UV-Initiated Bubble-Free Frontal Polymerization in Aqueous Conditions
Macromolecules, 2015, 48, 8738
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
1554755 CIFC22 H25 O5 PP -17.8931; 9.4542; 14.3399
89.1605; 82.9814; 69.4905
994.29Kim, Cheol-Eui; Son, Jeong-Yu; Shin, Seohyun; Seo, Boram; Lee, Phil Ho
Alkenylation of phosphacoumarins via aerobic oxidative Heck reactions and their synthetic application to fluorescent benzophosphacoumarins.
Organic letters, 2015, 17, 908-911
1554756 CIFC26 H23 B F4 N2 O2P 1 21/c 112.2068; 13.731; 14.626
90; 99.027; 90
2421.1Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554764 CIFC25 H20 B F4 N OP 1 21/n 110.72; 18.331; 12.174
90; 110.527; 90
2240.4Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554765 CIFC25 H21 B F4 N2 O2P 1 21/c 112.3471; 13.3272; 13.9786
90; 98.588; 90
2274.42Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554767 CIFC31 H24 Cl N O3P 1 21 17.081; 19.406; 9.491
90; 98.161; 90
1290.99Jayakumar, Samydurai; Kumarswamyreddy, Nandarapu; Prakash, Muthuraj; Kesavan, Venkitasamy
Palladium catalyzed asymmetric allylation of 3-OBoc-oxindoles: an efficient synthesis of 3-allyl-3-hydroxyoxindoles.
Organic letters, 2015, 17, 1066-1069
1554773 CIFC49.05 H59.38 Cl5.87 Li0.15 N3 P3 Ti2P -110.3083; 14.3567; 19.2355
75.287; 74.747; 84.913
2655.7Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.
Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.
Organic letters, 2015, 17, 752-755
1554774 CIFC16 H19 Cl3 N P TiP -18.8951; 9.2936; 13.0036
79.226; 76.069; 64.74
939.24Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.
Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.
Organic letters, 2015, 17, 752-755
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
1554782 CIFC34 H29 N5 O4 SP -19.7972; 10.509; 15.4371
72.931; 74.564; 84.268
1464.2Du, Zao; Xing, Yanpeng; Lu, Ping; Wang, Yanguang
Copper-catalyzed cascade double C3-indolations of 3-diazoindolin-2-imines with indoles: convenient access to 3,3-diaryl-2-iminoindoles.
Organic letters, 2015, 17, 1192-1195
1554783 CIFC24 H27 N3 O2P 1 21/c 117.5333; 9.245; 13.3467
90; 107.946; 90
2058.18Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B
One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.
Organic letters, 2015, 17, 1184-1187
1554791 CIFC21 H15 N3 OP 1 21/c 110.5706; 17.3802; 10.1316
90; 96.996; 90
1847.5Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B
One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.
Organic letters, 2015, 17, 1184-1187
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
1554794 CIFC19 H24 N2 OP c a 2112.8993; 10.853; 11.6466
90; 90; 90
1630.5Li, Bo; Wang, Si-Qing; Liu, Bin; Shi, Bing-Feng
Synthesis of oxazolines from amides via palladium-catalyzed functionalization of unactivated C(sp(3))-H bond.
Organic letters, 2015, 17, 1200-1203
1554796 CIFC24 H44 B2 N2 O4P b a m12.939; 13.093; 15.573
90; 90; 90
2638.2Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554797 CIFC29 H49 B2 Co N2 O4F d d 218.923; 58.36; 11.127
90; 90; 90
12288Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554798 CIFC24 H46 B2 N2 O5P 1 21/n 110.74; 19.626; 13.066
90; 93.197; 90
2749.8Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554802 CIFC24 H41 B2 O2 PP 1 21/n 18.6014; 17.6656; 16.4517
90; 107.162; 90
2388.51Bayardon, 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
1554803 CIFC28 H33 B2 Fe O2 PP 1 21 112.674; 9.2986; 12.919
90; 113.497; 90
1396.3Bayardon, 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
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
1554806 CIFC13 H12 O4P 1 21/n 110.5408; 14.0223; 15.567
90; 95.216; 90
2291.4Wang, Hong-Li; Shang, Ming; Sun, Shang-Zheng; Zhou, Zeng-Le; Laforteza, Brian N.; Dai, Hui-Xiong; Yu, Jin-Quan
Cu(II)-catalyzed coupling of aromatic C-H bonds with malonates.
Organic letters, 2015, 17, 1228-1231
1554809 CIFC19 H18 N O5 S2P -17.9459; 8.3713; 15.0845
98.477; 91.135; 97.754
982.54Deng, Zhimin; Wei, Jialiang; Liao, Lihao; Huang, Haiyan; Zhao, Xiaodan
Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: efficient synthesis of 3-amino allylic alcohols.
Organic letters, 2015, 17, 1834-1837
1554810 CIFC24 H22 O3C 1 c 114.8194; 23.1341; 17.3079
90; 104.994; 90
5731.7Gelat, Fabien; Richard, Vincent; Berger, Olivier; Montchamp, Jean-Luc
Development of a new family of chiral auxiliaries.
Organic letters, 2015, 17, 1819-1821
1554813 CIFC17 H16 Cl N3 OP -18.6811; 13.1015; 15.2298
66.74; 82.416; 77.876
1553.57Guo, Xiao; Chen, Wenteng; Chen, Binhui; Huang, Wei; Qi, Weixing; Zhang, Guolin; Yu, Yongping
One-pot three-component strategy for functionalized 2-aminoimidazoles via ring opening of α-nitro epoxides.
Organic letters, 2015, 17, 1157-1159
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
1554815 CIFC19 H21 F2 N OP 1 21/c 19.9286; 17.0093; 10.0841
90; 90.259; 90
1703He, Zhengbiao; Tan, Ping; Ni, Chuanfa; Hu, Jinbo
Fluoroalkylative aryl migration of conjugated N-arylsulfonylated amides using easily accessible sodium di- and monofluoroalkanesulfinates.
Organic letters, 2015, 17, 1838-1841
1554822 CIFC16 H10 N2 OP 1 21/n 16.4176; 20.0965; 9.335
90; 98.274; 90
1191.42Chen, Xiaopei; Cui, Xiuling; Yang, Fangfang; Wu, Yangjie
Base-promoted cross-dehydrogenative coupling of quinoline N-oxides with 1,3-azoles.
Organic letters, 2015, 17, 1445-1448
1554824 CIFC20 H14 O5P 1 21/n 19.0391; 9.7069; 17.2285
90; 102.573; 90
1475.41Tian, Yuan; Jiang, Nan; Zhang, Ai Hua; Chen, Chao Jun; Deng, Xin Zhao; Zhang, Wen Jing; Tan, Ren Xiang
Muta-mycosynthesis of naphthalene analogs.
Organic letters, 2015, 17, 1457-1460
1554830 CIFC20 H25 F3 N2 O3 SP 1 21/c 18.128; 15.344; 16.979
90; 102.44; 90
2067.8van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554831 CIFC22 H30 F3 N3 O3 SC 1 2/c 115.441; 10.924; 27.769
90; 90.9; 90
4683.4van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554832 CIFC18 H22 F3 N3 O3 SP 1 21/c 18.4815; 11.074; 21.3223
90; 93.426; 90
1999.1van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554833 CIFC21 H25 N3P -18.61; 9.179; 11.835
93.38; 95.73; 105.2
894.57van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554834 CIFC20 H26 N2P 1 21/c 18.693; 17.464; 11.525
90; 103.69; 90
1700van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554835 CIFC14 H22 N2R 3 c :H26.3163; 26.3163; 10.403
90; 90; 120
6239.3van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554837 CIFC49 H29 B F20 N O2 RhP 1 21/c 112.2787; 24.2002; 15.5541
90; 101.818; 90
4523.9Otley, Kate D.; Ellman, Jonathan A.
An efficient method for the preparation of styrene derivatives via Rh(III)-catalyzed direct C-H vinylation.
Organic letters, 2015, 17, 1332-1335
1554838 CIFC18 H18 O2P 1 21/c 114.026; 8.7035; 12.0599
90; 104.008; 90
1428.4Liu, Rui; Lu, Ze-Hai; Hu, Xiao-Hui; Li, Jun-Li; Yang, Xian-Jin
Monocarboxylation and intramolecular coupling of butenylated arenes via palladium-catalyzed C-H activation process.
Organic letters, 2015, 17, 1489-1492
1554839 CIFC17 H16 O2 SeP 1 21 16.9078; 10.3981; 10.0732
90; 95.471; 90
720.24Niu, Wenxue; Yeung, Ying-Yeung
Catalytic and highly enantioselective selenolactonization.
Organic letters, 2015, 17, 1660-1663
1554840 CIFC12 H20 O4P 3213.594; 13.594; 5.7493
90; 90; 120
920.11Wang, Hengbin; Negretti, Solymar; Knauff, Allison R.; Montgomery, John
Exo-selective reductive macrocyclization of ynals.
Organic letters, 2015, 17, 1493-1496
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
1554842 CIFC22 H18 F N3 O2 SP 1 21/c 115.7629; 11.6907; 10.7408
90; 100.958; 90
1943.22Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng
I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.
Organic letters, 2015, 17, 1521-1524
1554855 CIFC18 H21 N3 O2 S2P 1 21/c 110.0095; 11.563; 16.5773
90; 99.859; 90
1890.32Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng
I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.
Organic letters, 2015, 17, 1521-1524
1554856 CIFC20 H26 N2 O8 SiC 1 2/c 118.687; 6.709; 37.603
90; 90.534; 90
4714Yin, Zhiping; Liu, Zengjin; Huang, Zhenggang; Chu, Yang; Chu, Zhiwen; Hu, Jia; Gao, Lu; Song, Zhenlei
Synthesis of functionalized γ-lactone via Sakurai exo-cyclization/rearrangement of 3,3-bis(silyl) enol ester with a tethered acetal.
Organic letters, 2015, 17, 1553-1556
1554858 CIFC60 H85 I3 N10 O12P -114.2686; 14.6629; 17.0163
80.443; 70.781; 82.037
3301.6Saha, Subrata; Santra, Saikat; Ghosh, Pradyut
[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.
Organic letters, 2015, 17, 1854-1857
1554860 CIFC60 H78 Cl6 N10 O10C 1 2/c 122.9779; 30.564; 22.926
90; 114.207; 90
14685.1Saha, Subrata; Santra, Saikat; Ghosh, Pradyut
[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.
Organic letters, 2015, 17, 1854-1857
1554862 CIFC27 H27 F3 N2 O8P -18.5362; 11.0883; 14.8339
89.337; 75.808; 89.011
1360.96Huang, Lin; Zheng, Sheng-Cai; Tan, Bin; Liu, Xin-Yuan
Metal-free direct 1,6- and 1,2-difunctionalization triggered by radical trifluoromethylation of alkenes.
Organic letters, 2015, 17, 1589-1592
1554864 CIFC14 H11 N O7P n a 218.6933; 19.9383; 7.6281
90; 90; 90
1322.18Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Substituted quinoline quinones as surrogates for the PQQ cofactor: an electrochemical and computational study.
Organic letters, 2015, 17, 1850-1853
1554867 CIFC23 H26 Br N O4 SP 1 21 19.8067; 9.9678; 11.8916
90; 104.237; 90
1126.7Serpier, Fabien; Flamme, Benjamin; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain
Chiral pyrrolidines and piperidines from enantioselective rhodium-catalyzed cascade arylative cyclization.
Organic letters, 2015, 17, 1720-1723
1554869 CIFC28 H19 N O3 S2P -110.443; 11.228; 11.795
70.186; 87.728; 65.484
1175.6Ming, Wenbo; Liu, Xiaocui; Wang, Lianjie; Liu, Jun; Wang, Mang
Tandem Thien- and benzannulations of α-alkenoyl-α-alkynyl ketene dithioacetals with cyanoacetates: synthesis of functionalized benzo[b]thiophenes.
Organic letters, 2015, 17, 1746-1749
1554871 CIFC15 H21 N O3P 1 21/n 15.1627; 14.8595; 17.7219
90; 96.198; 90
1351.59Borrero, Nicholas V.; DeRatt, Lindsey G.; Ferreira Barbosa, Lais; Abboud, Khalil A.; Aponick, Aaron
Tandem gold-catalyzed dehydrative cyclization/diels-alder reactions: facile access to indolocarbazole alkaloids.
Organic letters, 2015, 17, 1754-1757
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
1554875 CIFC12 H13 Br O2P 1 21/c 16.0066; 11.7969; 16.772
90; 97.594; 90
1178Che, Chao; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.
Organic letters, 2015, 17, 1617-1620
1554877 CIFC23 H21 NP 1 21/c 110.4176; 11.9596; 16.0413
90; 114.231; 90
1822.51Che, Chao; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.
Organic letters, 2015, 17, 1617-1620
1554878 CIFC29 H36 N2 O4P 1 21 18.527; 16.7982; 9.3056
90; 102.717; 90
1300.22Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier
A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.
Organic letters, 2015, 17, 2054-2057
1554880 CIFC13 H22 O2C 1 c 114.0887; 10.5929; 9.0247
90; 114.771; 90
1222.92Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier
A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.
Organic letters, 2015, 17, 2054-2057
1554885 CIFC20 H20 Br2 Cl2 N2 O4P 15.0746; 14.828; 16.699
65.191; 89.579; 80.838
1123.5Shemet, 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
1554887 CIFC13 H15 Br Cl N O3P 1 21 14.8035; 8.2644; 18.363
90; 94.441; 90
726.79Shemet, 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
1554890 CIFC13 H16 Br Cl2 N O3P 1 21 110.669; 4.7706; 15.964
90; 107.952; 90
773Shemet, 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
1554894 CIFC6 H12 Cl2 O2P 1 21 14.9886; 19.578; 9.0155
90; 92.03; 90
880Shemet, 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
1554896 CIFC13 H15 Br Cl N O3P 1 21 112.2792; 4.9357; 13.4763
90; 115.38; 90
737.92Shemet, 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
1554898 CIFC13 H15 Br Cl N O3C 1 2 116.929; 4.841; 36.446
90; 101.211; 90
2930Shemet, 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
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
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
1554904 CIFC18 H14 N2 OP 1 21/c 117.283; 5.72; 16.0086
90; 115.367; 90
1430Bunescu, Ala; Wang, Qian; Zhu, Jieping
Synthesis of functionalized epoxides by copper-catalyzed alkylative epoxidation of allylic alcohols with alkyl nitriles.
Organic letters, 2015, 17, 1890-1893
1554907 CIFC28 H36 N2 O10 Pd3P 1 21/c 18.2684; 13.1049; 14.9823
90; 98.209; 90
1606.8Guo, Kun; Chen, Xiaolan; Guan, Mingyu; Zhao, Yingsheng
Direct ortho-C-H functionalization of aromatic alcohols masked by acetone oxime ether via exo-palladacycle.
Organic letters, 2015, 17, 1802-1805
1554909 CIFC21 H24 B N O2P 1 21/n 19.82013; 15.1033; 12.9881
90; 93.8267; 90
1922.05Pareek, Manish; Fallon, Thomas; Oestreich, Martin
Platinum(0)-Catalyzed Indolyne Insertion into Bis(pinacolato)diboron Followed by Site-Selective Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 2082-2085
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
1554914 CIFC25 H36 F3 N3 O4P -17.9555; 12.7291; 14.1773
101.894; 105.578; 101.34
1304Geoghegan, 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
1554915 CIFC20 H27 F3 N2 O3P 1 21/c 19.676; 6.0187; 35.338
90; 90.313; 90
2057.9Geoghegan, 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
1554916 CIFC18 H23 F3 N2 O3P -18.4082; 8.9935; 12.6932
109.241; 90.111; 102.16
883.25Geoghegan, 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
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
1554920 CIFC21 H16 N2 O2 SC 1 c 113.529; 16.7566; 8.6938
90; 116.175; 90
1768.8Lee, Dong Jin; Yoo, Eun Jeong
Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.
Organic letters, 2015, 17, 1830-1833
1554921 CIFC24 H24 N2 O2 SP 1 21/c 112.5268; 10.8502; 16.3904
90; 103.482; 90
2166.4Lee, Dong Jin; Yoo, Eun Jeong
Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.
Organic letters, 2015, 17, 1830-1833
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
1554926 CIFC19 H16 N2 O4P 1 21 17.5248; 11.7969; 18.7512
90; 98.035; 90
1648.2Bisai, Vishnumaya; Unhale, Rajshekhar A.; Suneja, Arun; Dhanasekaran, Sivasankaran; Singh, Vinod K.
An Efficient Entry to syn- and anti-Selective Isoindolinones via an Organocatalytic Direct Mannich/Lactamization Sequence.
Organic letters, 2015, 17, 2102-2105
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
1554932 CIFC18 H19 Cl F3 N O SP 1 21 111.7646; 15.4251; 12.0356
90; 118.452; 90
1920.3Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554934 CIFC19 H23 Fe N O2 SP 1 21 15.84461; 11.3132; 13.829
90; 95.4227; 90
910.298Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554935 CIFC23 H17 Cl O2P 1 21/m 19.353; 7.448; 12.251
90; 93.725; 90
851.6Liu, Yang; Jin, Shiyu; Huang, Liping; Hu, Youhong
Phase transfer reagent promoted tandem ring-opening and ring-closing reactions of unique 3-(1-alkynyl) chromones.
Organic letters, 2015, 17, 2134-2137
1554937 CIFC133 H116 N8 O21 S4P 1 21 110.8299; 17.8426; 16.7462
90; 105.418; 90
3119.5Xie, Danbo; Yang, Limin; Lin, Youqiang; Zhang, Zhiming; Chen, Dongdong; Zeng, Xiaofei; Zhong, Guofu
Rapid access to spirocylic oxindoles: application of asymmetric N-heterocyclic carbene-catalyzed [3 + 3] cycloaddition of imines to oxindole-derived enals.
Organic letters, 2015, 17, 2318-2321
1554941 CIFC39 H30 Cl N OP 1 21/n 114.7817; 10.4931; 20.1054
90; 110.04; 90
2929.66Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554944 CIFC24 H24 Cl N OP 1 21/n 112.0241; 10.8634; 15.0306
90; 92.829; 90
1960.94Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554948 CIFC24 H24 Cl N OP 1 21/c 116.3879; 7.0026; 17.8667
90; 103.718; 90
1991.86Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554950 CIFC152.5 H199 B4 N7 O23P 1 21/c 111.705; 28.512; 22.406
90; 98.94; 90
7387Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554955 CIFC50 H44 F24 N4 P4P 1 21/n 113.488; 14.281; 14.287
90; 108.36; 90
2611.9Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554956 CIFC186 H168 B4 N14 O31P -116.134; 16.609; 16.766
85.82; 65.15; 75.26
3939.7Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554959 CIFC117 H171 B4 N4 O20P 1 21/c 142.193; 8.356; 15.63
90; 90.76; 90
5510.1Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554960 CIFC180 H112 B4 D84 N4 O34 S14P -116.67; 17.44; 19.659
81.21; 74.06; 62.19
4859Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554968 CIFC70 H56 N8 O8P -111.446; 13.451; 22.036
98.71; 104.3; 98.36
3189.9Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554969 CIFC32 H26 N4 O2C 1 2/c 116.098; 8.0852; 19.417
90; 103.12; 90
2461.3Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554971 CIFC34 H30 N4 O4P 1 21/c 17.3964; 23.302; 16.073
90; 94.05; 90
2763.3Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554973 CIFC70 H58 Cl6 N8 O12 SC 1 c 137.78; 8.9173; 26.953
90; 133.41; 90
6596Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554978 CIFC16 H10 Br N O4P 1 21/c 112.4447; 15.6502; 7.9646
90; 105.739; 90
1493Bag, Raghunath; Sar, Dinabandhu; Punniyamurthy, Tharmalingam
Copper(II)-catalyzed direct dioxygenation of alkenes with air and N-hydroxyphthalimide: synthesis of β-keto-N-alkoxyphthalimides.
Organic letters, 2015, 17, 2010-2013
1554981 CIFC70 H120 N14 O26 S8P -113.0106; 13.1402; 14.3888
80.344; 63.999; 78.993
2160.42Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554982 CIFC30 H60 N12 O16 S4C 1 2/c 113.4741; 14.6965; 22.6791
90; 92.704; 90
4485.96Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554988 CIFC40 H69.97 N4 O14 S4P -111.2634; 15.966; 16.009
111.587; 100.691; 109.004
2373.6Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
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
1554994 CIFC28 H23 N3 O4 SP 1 21/n 112.8623; 11.3355; 16.9579
90; 94.493; 90
2464.87Chen, Jing; Li, Jianjun; Wang, Jiazhe; Li, Hao; Wang, Wei; Guo, Yuewei
Phosphine-Catalyzed Aza-MBH Reactions of Vinylpyridines: Efficient and Rapid Access to 2,3,5-Triarylsubstituted 3-Pyrrolines.
Organic letters, 2015, 17, 2214-2217
1554996 CIFC19 H22 O7P 1 21/n 16.0808; 23.3393; 12.5225
90; 94.028; 90
1772.82Tan, Ceheng; Chen, Wei; Mu, Xinpeng; Chen, Qi; Gong, Jianxian; Luo, Tuoping; Yang, Zhen
Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I.
Organic letters, 2015, 17, 2338-2341
1554998 CIFC26 H31 Br N2 O3P -19.6121; 11.761; 13.648
98.331; 109.571; 113.637
1260.2Zeng, Xiao-Hua; Wang, Hong-Mei; Ding, Ming-Wu
Unexpected Synthesis of 5,6-Dihydropyridin-2(1H)-ones by a Domino Ugi/Aldol/Hydrolysis Reaction Starting from Baylis-Hillman Phosphonium Salts.
Organic letters, 2015, 17, 2234-2237
1555000 CIFC38 H44 B2 F4 N4 O6P -19.7881; 13.2333; 16.5195
67.596; 77.669; 72.069
1870.86Huaulmé, Quentin; Mirloup, Antoine; Retailleau, Pascal; Ziessel, Raymond
Synthesis of Highly Functionalized BOPHY Chromophores Displaying Large Stokes Shifts.
Organic letters, 2015, 17, 2246-2249
1555003 CIFC27 H30 F N O2P -19.3088; 9.5092; 14.5742
92.724; 104.673; 110
1159.92Davies, 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
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
1555005 CIFC28 H32 N4 O2P 32 2 111.32263; 11.32263; 35.383
90; 90; 120
3928.44Davies, 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
1555006 CIFC30 H35 N O4P 19.7073; 10.168; 14.0374
85.597; 85.998; 82.306
1366.53Davies, 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
1555007 CIFC28 H31 F2 N O2P 110.4764; 10.6867; 12.3768
85.757; 70.552; 69.477
1222.26Davies, 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
1555008 CIFC28 H31 F2 N O2P 1 21 17.90952; 16.3522; 9.53794
90; 95.6737; 90
1227.58Davies, 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
1555011 CIFC23 H27 Br N2 O5P 1 21/n 18.3956; 11.6027; 23.715
90; 91.1454; 90
2309.7Arai, Takayoshi; Tsuchiya, Kento; Matsumura, Eri
PyBidine-NiCl2-Catalyzed Asymmetric Addition of Alcohols and Peroxides to Isatin-Derived Ketimines.
Organic letters, 2015, 17, 2416-2419
1555012 CIFC8 H11 F3 N2 O SP 1 21/c 18.4044; 11.3774; 11.5451
90; 96.16; 90
1097.6Liang, Zhaoli; Wang, Fei; Chen, Pinhong; Liu, Guosheng
Copper-Catalyzed Intermolecular Trifluoromethylthiocyanation of Alkenes: Convenient Access to CF3-Containing Alkyl Thiocyanates.
Organic letters, 2015, 17, 2438-2441
1555018 CIFC76 H112 F14 N4 Sn4P -110.7975; 11.121; 17.986
82.945; 76.059; 70.925
1978.74Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.
Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.
Organic letters, 2015, 17, 2266-2269
1555019 CIFC32 H4 F26 N4P -16.15317; 9.3804; 13.8177
103.878; 100.265; 98.23
747.31Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.
Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.
Organic letters, 2015, 17, 2266-2269
1555021 CIFC19 H18 O2P n a 2112.91; 9.664; 12.157
90; 90; 90
1516.7Lewis, 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
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
1555026 CIFC22 H21 N O3P -19.724; 10.178; 10.676
62.165; 79.328; 69.089
872.6Capreti, Naylil M. R.; Jurberg, Igor D.
Michael Addition of Soft Carbon Nucleophiles to Alkylidene Isoxazol-5-ones: A Divergent Entry to β-Branched Carbonyl Compounds.
Organic letters, 2015, 17, 2490-2493
1555028 CIFC15 H13 N OR -3 :H26.4383; 26.4383; 8.6956
90; 90; 120
5263.8Zhang, Yan; Wang, Dahai; Cui, Sunliang
Facile Synthesis of Isoindolinones via Rh(III)-Catalyzed One-Pot Reaction of Benzamides, Ketones, and Hydrazines.
Organic letters, 2015, 17, 2494-2497
1555031 CIFC36 H39 N O2P 1 21/c 114.8225; 11.0736; 18.657
90; 100.056; 90
3015.3Reddy, Virsinha; Vijaya Anand, Ramasamy
Expedient Access to Unsymmetrical Diarylindolylmethanes through Palladium-Catalyzed Domino Electrophilic Cyclization-Extended Conjugate Addition Approach.
Organic letters, 2015, 17, 3390-3393
1555034 CIFC25 H27 Fe N O3 SP 1 21 115.0789; 8.6357; 18.2167
90; 106.122; 90
2278.8Ogasawara, Masamichi; Wada, Shiro; Isshiki, Erika; Kamimura, Takumi; Yanagisawa, Akira; Takahashi, Tamotsu; Yoshida, Kazuhiro
Enantioselective synthesis of planar-chiral ferrocene-fused 4-pyridones and their application in construction of pyridine-based organocatalyst library.
Organic letters, 2015, 17, 2286-2289
1555037 CIFC17 H14 N2 O3P 1 21/c 18.9224; 9.3813; 18.2533
90; 103.064; 90
1488.32Son, Jeong-Yu; Kim, Sunghwa; Jeon, Woo Hyung; Lee, Phil Ho
Synthesis of Cinnolin-3(2H)-one Derivatives from Rh-Catalyzed Reaction of Azobenzenes with Diazotized Meldrum's Acid.
Organic letters, 2015, 17, 2518-2521
1555039 CIFC26 H28 O5P -110.896; 11.118; 11.442
109.812; 100.766; 111.223
1137.4Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula
Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.
Organic letters, 2015, 17, 3446-3449
1555041 CIFC23 H24 O3P -18.428; 11.011; 11.459
65.415; 87.993; 89.668
966.4Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula
Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.
Organic letters, 2015, 17, 3446-3449
1555044 CIFC21 H36 O4 SiC 1 2 122.265; 7.7011; 12.8529
90; 102.095; 90
2154.9Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555045 CIFC12 H14 O3P 1 21/c 112.324; 7.8713; 10.6532
90; 92.217; 90
1032.65Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555051 CIFC36 H55 N O7 Si2P -18.9128; 10.9914; 20.184
91.339; 96.624; 104.357
1899.99Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
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
1555053 CIFC21 H38 O5 SP 1 21/c 116.4753; 10.1532; 13.8282
90; 98.669; 90
2286.71Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555059 CIFC15 H22 O6P 1 21/n 18.5281; 18.7862; 9.5185
90; 100.368; 90
1500.07Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555060 CIFC16 H17 N O4P 1 21 16.9082; 11.2913; 19.3834
90; 91.357; 90
1511.53Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555061 CIFC34 H22 Cl2 N4 O4P b c a10.6177; 21.038; 26.249
90; 90; 90
5863.4Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555077 CIFC30 H22 Cl2 N4 O12P 4310.6627; 10.6627; 29.5381
90; 90; 90
3358.3Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555078 CIFC29 H20 I4 O4P -112.1779; 21.8512; 21.9539
60.52; 87.603; 86.921
5077.5Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555080 CIFC38 H26 Cl2 O4P 1 21/c 113.2235; 24.195; 10.2868
90; 110.556; 90
3081.6Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555083 CIFC19 H21 N O4 SP 1 21/n 18.2569; 11.0688; 20.1396
90; 95.9683; 90
1830.66Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi
Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.
Organic letters, 2015, 17, 3498-3501
1555086 CIFC27 H27 N O5 SP 1 21/n 110.98; 21.409; 11.347
90; 104.07; 90
2587.3Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi
Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.
Organic letters, 2015, 17, 3498-3501
1555089 CIFC38 H34 P2P -18.6263; 12.097; 16.023
107.86; 95.73; 104.279
1514.1Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François
Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.
Organic letters, 2015, 17, 3518-3520
1555090 CIFC32 H32 O P2P 1 21/c 114.7596; 10.4392; 17.7877
90; 105.924; 90
2635.5Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François
Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.
Organic letters, 2015, 17, 3518-3520
1555091 CIFC18 H23 N O2P 1 21/c 112.58; 15.83; 8.839
90; 109.551; 90
1658.7Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian
Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2015, 17, 3544-3547
1555095 CIFC19 H16 O2C 1 2 117.095; 5.874; 15.476
90; 106; 90
1493.8Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian
Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2015, 17, 3544-3547
1555096 CIFC21 H13 Cl I3 N O2P -18.885; 11.599; 11.638
87.07; 72.279; 76.183
1109.11Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu
Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.
Organic letters, 2015, 17, 3576-3579
1555100 CIFC21 H15 Cl I N O2P 1 21/n 111.057; 13.631; 13.716
90; 110.38; 90
1937.8Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu
Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.
Organic letters, 2015, 17, 3576-3579
1555102 CIFC22 H22 OP -19.1622; 9.508; 10.568
83; 65.519; 78.417
820Manojveer, Seetharaman; Balamurugan, Rengarajan
In Situ Formed Acetal-Facilitated Synthesis of Substituted Indene Derivatives from o-Alkenylbenzaldehydes.
Organic letters, 2015, 17, 3600-3603
1555105 CIFC8 H10 O4P c a 2110.571; 5.838; 12.338
90; 90; 90
761.4Rashid, 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
1555106 CIFC12 H14 O6F d d 237.2102; 18.06; 6.8155
90; 90; 90
4580.1Rashid, 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
1555107 CIFC10 H12 O3P b c a8.8394; 8.5924; 23.437
90; 90; 90
1780.1Rashid, 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
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
1555109 CIFC8 H10 O4P 1 21 15.3883; 12.812; 6.0438
90; 114.32; 90
380.21Rashid, 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
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
1555114 CIFC18 H23 N O5 SP 18.6291; 9.4332; 12.4474
82.659; 70.506; 68.236
887.04Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555119 CIFC12 H15 F N2 O4 SP 1 21/n 16.70613; 8.92562; 21.9646
90; 91.7362; 90
1314.12Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555122 CIFC11 H14 N2 O2 SP 1 21/n 115.2033; 5.10542; 15.6074
90; 108.006; 90
1152.1Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555124 CIFC16 H16 N2 O2 SP 1 21/n 18.236; 21.1919; 8.4904
90; 103.856; 90
1438.76Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
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
1555128 CIFC14 H17 Br Cl N O4 SP 1 21 19.24; 6.262; 14.504
90; 91.561; 90
838.9Liu, 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
1555130 CIFC20 H24 Br N O4 SP 1 21 114.656; 10.051; 14.998
90; 104.87; 90
2135.3Liu, 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
1555133 CIFC14 H18 Br N O4 SP 1 21 16.4495; 15.276; 8.0516
90; 96.47; 90
788.2Liu, 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
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
1555135 CIFC40 H41 N O4 S2P -111.0456; 12.0988; 14.8761
68.867; 70.725; 86.448
1746.7Ding, 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
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
1555151 CIFC21 H23 N OP 1 21/c 19.1308; 14.0389; 14.7904
90; 106.943; 90
1813.6Sinai, Ádám; Vangel, Dóra; Gáti, Tamás; Bombicz, Petra; Novák, Zoltán
Utilization of Copper-Catalyzed Carboarylation-Ring Closure for the Synthesis of New Oxazoline Derivatives.
Organic letters, 2015, 17, 4136-4139
1555154 CIFC14 H11 Cl N2P 1 21/n 115.4081; 7.7461; 19.9246
90; 98.208; 90
2353.69Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555155 CIFC19 H14 Cl N2 O PP 1 21/c 111.949; 8.5662; 17.479
90; 103.621; 90
1738.8Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555158 CIFC7 H3 Cl2 N2P b c a11.4945; 7.5152; 17.4299
90; 90; 90
1505.66Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555161 CIFC23 H24 O4P 1 21/c 18.759; 21.523; 10.067
90; 104.55; 90
1837Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555162 CIFC18 H20 O6P 1 21/c 17.7505; 21.813; 9.5132
90; 94.65; 90
1603Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555163 CIFC16.5 H16 Cl1.5 N2 O3P 1 21/c 116.298; 11.852; 9.939
90; 90.99; 90
1919.6Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555165 CIFC17 H17 Br O5P b c a11.48; 10.279; 26.181
90; 90; 90
3089.4Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen
Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.
Organic letters, 2015, 17, 4184-4187
1555167 CIFC18 H20 O5P 1 21/c 110.526; 19.394; 7.8119
90; 96.58; 90
1584.2Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen
Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.
Organic letters, 2015, 17, 4184-4187
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
1555172 CIFC34 H30 N2 O6P 1 21/n 111.4637; 45.4434; 12.0124
90; 116.324; 90
5608.9Yan, Jianming; Tay, Guan Liang; Neo, Cuien; Lee, Bo Ra; Chan, Philip Wai Hong
Gold-Catalyzed Cycloisomerization and Diels-Alder Reaction of 1,6-Diyne Esters with Alkenes and Diazenes to Hydronaphthalenes and -cinnolines.
Organic letters, 2015, 17, 4176-4179
1555175 CIFC26 H18 N4 O5P -19.141; 10.706; 12.0986
73.26; 68.76; 72.31
1030.1Miura, Wataru; Hirano, Koji; Miura, Masahiro
Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.
Organic letters, 2015, 17, 4034-4037
1555177 CIFC21 H15 N3 O3P 1 21/c 116.334; 13.572; 7.87
90; 104.13; 90
1691.9Miura, Wataru; Hirano, Koji; Miura, Masahiro
Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.
Organic letters, 2015, 17, 4034-4037
1555181 CIFC24 H19 N2 O2 S2P 1 21/c 18.3103; 22.0934; 11.8386
90; 104.267; 90
2106.56Chen, 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
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
1555188 CIFC19 H20 Cl N O2 SP 1 21 110.133; 9.753; 19.638
90; 100.289; 90
1909.6Huang, 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
1555196 CIFC21 H19 N3 OP b c a12.7097; 15.6515; 17.3613
90; 90; 90
3453.6Takamatsu, 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
1555197 CIFC22 H34 N4 O9P -19.7492; 10.793; 12.316
106.75; 97.22; 95.45
1219.3Jia, Yan-Lai; Wei, Mei-Yan; Chen, Hai-Yan; Guan, Fei-Fei; Wang, Chang-Yun; Shao, Chang-Lun
(+)- and (-)-Pestaloxazine A, a Pair of Antiviral Enantiomeric Alkaloid Dimers with a Symmetric Spiro[oxazinane-piperazinedione] Skeleton from Pestalotiopsis sp.
Organic letters, 2015, 17, 4216-4219
1555206 CIFC26 H24 N4 O4C 1 c 19.0718; 20.806; 12.975
90; 107.07; 90
2341.1Liu, Honglei; Yuan, Chunhao; Wu, Yang; Xiao, Yumei; Guo, Hongchao
Sc(OTf)3-Catalyzed [3 + 3] Cycloaddition of Cyclopropane 1,1-Diesters with Phthalazinium Dicyanomethanides.
Organic letters, 2015, 17, 4220-4223
1555207 CIFC42 H22 F6P -19.9256; 11.9918; 12.9082
90.335; 100.557; 103.488
1466.85Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.
Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.
Organic letters, 2015, 17, 4224-4227
1555208 CIFC42 H22 F6P b c a9.5341; 17.1742; 34.8068
90; 90; 90
5699.3Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.
Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.
Organic letters, 2015, 17, 4224-4227
1555211 CIFC65 H65 Cl3 N4 O6 ZnP 4318.5406; 18.5406; 21.1268
90; 90; 90
7262.4Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555213 CIFC70 H77 Cl1.5 N4 O5 ZnC 1 2/c 139.3331; 14.7758; 28.6914
90; 131.696; 90
12450.8Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555214 CIFC67 H71 N4 O5 ZnP -116.9996; 24.3355; 32.7331
89.3681; 83.194; 89.522
13444.9Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555216 CIFC14 H11 N3C 1 2/c 114.857; 12.127; 13.289
90; 106.898; 90
2290.9Jia, Feng-Cheng; Zhou, Zhi-Wen; Xu, Cheng; Cai, Qun; Li, Deng-Kui; Wu, An-Xin
Expeditious Synthesis of 2-Phenylquinazolin-4-amines via a Fe/Cu Relay-Catalyzed Domino Strategy.
Organic letters, 2015, 17, 4236-4239
1555218 CIFC33 H23 Cl3 N2 O2P 1 21 19.07268; 11.9732; 13.4535
90; 106.945; 90
1397.99Takaishi, 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
1555219 CIFC32.5 H26 N2 O3.5P 21 21 211.4574; 24.0028; 9.1294
90; 90; 90
2510.67Takaishi, 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
1555220 CIFC34 H24 O2P 21 21 211.1679; 24.1852; 9.1499
90; 90; 90
2471.37Takaishi, 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
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
1555223 CIFC245 H138 Cl10 F24 N8 O32 S8P -116.057; 18.336; 18.879
79.909; 74.398; 79.264
5214Węcławski, Marek K; Meiling, Till T.; Leniak, Arkadiusz; Cywiński, Piotr J; Gryko, Daniel T.
Planar, Fluorescent Push-Pull System That Comprises Benzofuran and Iminocoumarin Moieties.
Organic letters, 2015, 17, 4252-4255
1555224 CIFC41 H36 N2 O9P 1 21/c 119.0503; 11.68507; 14.8134
90; 92.939; 90
3293.19Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming
Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.
Organic letters, 2015, 17, 4102-4105
1555225 CIFC40 H32 N2 O9P b c a13.9815; 16.6793; 26.5582
90; 90; 90
6193.4Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming
Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.
Organic letters, 2015, 17, 4102-4105
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
1555227 CIFC24 H25 F3 I N O4 SP 1 21/c 113.4658; 20.2837; 19.439
90; 100.921; 90
5213.3Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555229 CIFC24 H26 F2 I N O4 SP 1 21/n 112.121; 15.7186; 25.7853
90; 91.321; 90
4911.4Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555230 CIFC23 H25 F2 I N2 O4 SP n a 2124.1416; 10.1959; 20.5376
90; 90; 90
5055.2Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555231 CIFC16 H26 O6P 1 21 16.5502; 13.639; 9.1291
90; 91.21; 90
815.4Hwang, In Hyun; Swenson, Dale C.; Gloer, James B.; Wicklow, Donald T.
Pestaloporonins: Caryophyllene-Derived Sesquiterpenoids from a Fungicolous Isolate of Pestalotiopsis sp.
Organic letters, 2015, 17, 4284-4287
1555233 CIFC22 H36 O6 SiP 1 21 16.395; 46.881; 8.2621
90; 111.164; 90
2309.9Clark, J. Stephen; Romiti, Filippo; Sieng, Bora; Paterson, Laura C.; Stewart, Alister; Chaudhury, Subhabrata; Thomas, Lynne H.
Synthesis of the A-D Ring System of the Gambieric Acids.
Organic letters, 2015, 17, 4694-4697
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
1555237 CIFC23 H23 F N2 O6P -17.9045; 11.1779; 11.7527
91.21; 92.807; 94
1034.33Navuluri, Chandrasekhar; Charette, André B
Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.
Organic letters, 2015, 17, 4288-4291
1555241 CIFC76 H48 O4C 2 2 219.5716; 40.233; 14.5609
90; 90; 90
5607.3Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555242 CIFC26 H18 O2C 2 2 219.6233; 28.1324; 14.4388
90; 90; 90
3908.97Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555243 CIFC26 H18 Br2 O2C 2 2 219.5385; 16.362; 14.106
90; 90; 90
2201.5Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555244 CIFC76 H78 O16 S4P 43 21 213.3557; 13.3557; 44.138
90; 90; 90
7873.1Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
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
1555251 CIFC18 H16 O SP 1 21/n 15.3543; 15.615; 17.226
90; 93.57; 90
1437.4Zhao, Peng; Liu, Yu; Xi, Chanjuan
MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.
Organic letters, 2015, 17, 4388-4391
1555254 CIFC24 H16 O SP 1 21/c 19.1038; 11.532; 16.523
90; 101.54; 90
1699.6Zhao, Peng; Liu, Yu; Xi, Chanjuan
MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.
Organic letters, 2015, 17, 4388-4391
1555256 CIFC21 H30 O4 SiP 1 21/c 115.86; 8.9849; 32.138
90; 117.571; 90
4059.6Khatri, Buddha B.; Sieburth, Scott McN
Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.
Organic letters, 2015, 17, 4360-4363
1555257 CIFC20 H28 O3 SiC 1 2/c 134.403; 6.7764; 16.1333
90; 92.333; 90
3758Khatri, Buddha B.; Sieburth, Scott McN
Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.
Organic letters, 2015, 17, 4360-4363
1555258 CIFC9 H5 Cl2 N3 SP b c a6.9189; 13.8264; 21.5767
90; 90; 90
2064.1Kalogirou, Andreas S.; Manoli, Maria; Koutentis, Panayiotis A.
Synthesis of N-Aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines from 3,4,4,5-Tetrachloro-4H-1,2,6-thiadiazine.
Organic letters, 2015, 17, 4118-4121
1555276 CIFC23 H42 N4 O9P 3213.414; 13.414; 13.869
90; 90; 120
2161Ganesh 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
1555277 CIFC32.33333 H57.66667 N6 O12.66667P 115.4725; 16.0538; 16.749
107.8; 106.461; 106.157
3482.3Ganesh 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
1555278 CIFC39 H70 N8 O15P 1 21 19.319; 23.446; 11.396
90; 108.442; 90
2362.1Ganesh 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
1555279 CIFC37 H54 N6 O8P 1 21 111.813; 9.272; 19.747
90; 104.524; 90
2093.8Ganesh 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
1555280 CIFC44 H71 N7 O12P 6127.637; 27.637; 11.845
90; 90; 120
7835Ganesh 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
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
1555283 CIFC18 H28 O7P 1 21 19.874; 10.305; 18.765
90; 99.09; 90
1885.4Chaudhary, Sandeep; Sharma, Vashundhra; Jaiswal, Pradeep K.; Gaikwad, Anil N.; Sinha, Sudhir K.; Puri, Sunil K.; Sharon, Ashoke; Maulik, Prakas R.; Chaturvedi, Vinita
Stable Tricyclic Antitubercular Ozonides Derived from Artemisinin.
Organic letters, 2015, 17, 4948-4951
1555284 CIFC19 H29 N OC 1 2/c 127.579; 8.3362; 17.969
90; 122.94; 90
3467Cheng, Yong-Feng; Rong, Hao-Jie; Yi, Cheng-Bo; Yao, Jun-Jun; Qu, Jin
Redox-Triggered α-C-H Functionalization of Pyrrolidines: Synthesis of Unsymmetrically 2,5-Disubstituted Pyrrolidines.
Organic letters, 2015, 17, 4758-4761
1555291 CIFC28 H22 Cl N2 O2 P SP 1 21/n 19.87691; 17.4624; 14.111
90; 101.632; 90
2383.81Takada, Hisashi; Kumagai, Naoya; Shibasaki, Masakatsu
Stereoselective Total Synthesis of KAE609 via Direct Catalytic Asymmetric Alkynylation to Ketimine.
Organic letters, 2015, 17, 4762-4765
1555293 CIFC9 H7 N O2P 1 21/n 14.4189; 10.48312; 16.03096
90; 95.3299; 90
739.405Liu, Wei; Li, Hou-Jin; Xu, Meng-Yang; Ju, Ying-Chen; Wang, Lai-You; Xu, Jun; Yang, De-Po; Lan, Wen-Jian
Pseudellones A-C, Three Alkaloids from the Marine-Derived Fungus Pseudallescheria ellipsoidea F42-3.
Organic letters, 2015, 17, 5156-5159
1555294 CIFC14 H13 N3 O3 SP n a 218.9685; 11.8374; 12.3725
90; 90; 90
1313.51Liu, Wei; Li, Hou-Jin; Xu, Meng-Yang; Ju, Ying-Chen; Wang, Lai-You; Xu, Jun; Yang, De-Po; Lan, Wen-Jian
Pseudellones A-C, Three Alkaloids from the Marine-Derived Fungus Pseudallescheria ellipsoidea F42-3.
Organic letters, 2015, 17, 5156-5159
1555296 CIFC21 H22 N2 O6 SP -110.449; 10.564; 10.913
65.028; 72.368; 76.052
1031.7Xu, Changming; Zhang, Long; Luo, Sanzhong
Catalytic Asymmetric Oxidative α-C-H N,O-Ketalization of Ketones by Chiral Primary Amine.
Organic letters, 2015, 17, 4392-4395
1555300 CIFC35 H44 N6 O9 SP -18.5759; 13.69; 15.1168
94.615; 91.322; 103.134
1721.18Dabrowa, Kajetan; Niedbala, Patryk; Majdecki, Maciej; Duszewski, Piotr; Jurczak, Janusz
A General Method for Synthesis of Unclosed Cryptands via H-Bond Templated Macrocyclization and Subsequent Mild Postfunctionalization.
Organic letters, 2015, 17, 4774-4777
1555301 CIFC34 H43 N7 O11 SP 1 21/n 113.5559; 16.9708; 16.5586
90; 103.987; 90
3696.43Dabrowa, Kajetan; Niedbala, Patryk; Majdecki, Maciej; Duszewski, Piotr; Jurczak, Janusz
A General Method for Synthesis of Unclosed Cryptands via H-Bond Templated Macrocyclization and Subsequent Mild Postfunctionalization.
Organic letters, 2015, 17, 4774-4777
1555303 CIFC10 H9 N3 OP 1 21/n 117.897; 4.7536; 21.443
90; 105.729; 90
1756Nguyen, Thanh Binh; Corbin, Mathilde; Retailleau, Pascal; Ermolenko, Ludmila; Al-Mourabit, Ali
Elements as Direct Feedstocks for Organic Synthesis: Fe/I2/O2 for Diamination of 2-Cyclohexenones with 2-Aminopyrimidine and 2-Aminopyridines.
Organic letters, 2015, 17, 4956-4959
1555304 CIFC36 H26 N2 O4 S2P -110.972; 11.356; 12.6933
105.75; 96.509; 100.348
1475.31Sumi, Takaki; Kaburagi, Tomohiro; Morimoto, Masakazu; Une, Kanako; Sotome, Hikaru; Ito, Syoji; Miyasaka, Hiroshi; Irie, Masahiro
Fluorescent Photochromic Diarylethene That Turns on with Visible Light.
Organic letters, 2015, 17, 4802-4805
1555305 CIFC36 H26 N2 O4 S2P -17.8828; 13.6596; 14.9014
112.825; 96.4272; 96.2488
1449.13Sumi, Takaki; Kaburagi, Tomohiro; Morimoto, Masakazu; Une, Kanako; Sotome, Hikaru; Ito, Syoji; Miyasaka, Hiroshi; Irie, Masahiro
Fluorescent Photochromic Diarylethene That Turns on with Visible Light.
Organic letters, 2015, 17, 4802-4805
1555306 CIFC18 H18 N2 O4P 1 21/c 111.3073; 12.3863; 11.762
90; 103.475; 90
1601.99Deng, Guisheng; Wang, Feng; Lu, Shengle; Cheng, Bo
Synthesis of Pyrano[3,2-c]pyrazol-7(1H)-one Derivatives by Tandem Cyclization of 2-Diazo-3,5-dioxo-6-ynoates (Ynones).
Organic letters, 2015, 17, 4651-4653
1555307 CIFC16 H22 O5P 1 21/c 113.19; 10.5762; 12.1985
90; 109.1; 90
1608Gao, Bao; Xie, Yinjun; Shen, Zhiqiang; Yang, Lei; Huang, Hanmin
Decarboxylative Alkylcarboxylation of α,β-Unsaturated Acids Enabled by Copper-Catalyzed Oxidative Coupling.
Organic letters, 2015, 17, 4968-4971
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
1555309 CIFC17 H12 N2 OP -16.9324; 8.0825; 12.0884
92.847; 95.144; 94.822
671.09Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark
Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.
Organic letters, 2015, 17, 4838-4841
1555310 CIFC19 H14 N2 OP b c a14.5086; 13.0756; 15.3147
90; 90; 90
2905.3Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark
Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.
Organic letters, 2015, 17, 4838-4841
1555311 CIFC21 H20 N2 O3P 1 21/c 19.9575; 10.3499; 34.9584
90; 95.625; 90
3585.4Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark
Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.
Organic letters, 2015, 17, 4838-4841
1555312 CIFC23 H22 N2 O3P 1 21/n 112.4989; 10.3089; 15.2366
90; 91.7; 90
1962.37Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark
Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.
Organic letters, 2015, 17, 4838-4841
1555313 CIFC25 H17 ClP 1 21 110.027; 5.4598; 16.953
90; 106.348; 90
890.6Mendis, Shehani N.; Tunge, Jon A.
Palladium-Catalyzed Stereospecific Decarboxylative Benzylation of Alkynes.
Organic letters, 2015, 17, 5164-5167
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
1555315 CIFC22 H17 PP 1 21 112.1722; 5.9237; 12.6791
90; 115.892; 90
822.45Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555316 CIFC22 H17 As Au ClP 1 21/c 18.5323; 19.1547; 12.0545
90; 99.9913; 90
1940.23Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555317 CIFC22 H17 Au Cl PP b c a9.915; 17.298; 22.652
90; 90; 90
3885Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555318 CIFC24 H21 As O2P n m a7.88163; 16.2823; 15.3253
90; 90; 90
1966.71Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555319 CIFC22 H17 AsP 1 21 112.2262; 6.03311; 12.5465
90; 115.216; 90
837.26Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555320 CIFC21 H17 NP c a 2120.9818; 8.85852; 8.04013
90; 90; 90
1494.4Yamada, Shinji; Yamamoto, Natsuo; Takamori, Eri
A Molecular Seesaw Balance: Evaluation of Solvent and Counteranion Effects on Pyridinium-π Interactions.
Organic letters, 2015, 17, 4862-4865
1555321 CIFC22 H20 B F4 NP -18.30165; 11.9912; 19.0328
81.1115; 89.9577; 75.0852
1807.32Yamada, Shinji; Yamamoto, Natsuo; Takamori, Eri
A Molecular Seesaw Balance: Evaluation of Solvent and Counteranion Effects on Pyridinium-π Interactions.
Organic letters, 2015, 17, 4862-4865
1555322 CIFC22 H20 I NP 1 21/c 18.35321; 18.1932; 12.3367
90; 109.572; 90
1766.51Yamada, Shinji; Yamamoto, Natsuo; Takamori, Eri
A Molecular Seesaw Balance: Evaluation of Solvent and Counteranion Effects on Pyridinium-π Interactions.
Organic letters, 2015, 17, 4862-4865
1555323 CIFC20 H16 Cl N3 O6P 1 21 16.5669; 20.611; 7.3177
90; 92.8; 90
989.3He, Fu-Sheng; Zhu, Han; Wang, Zheng; Gao, Ming; Yu, Xingxin; Deng, Wei-Ping
Asymmetric Construction of 3,4-Diamino Pyrrolidines via Chiral N,O-Ligand/Cu(I) Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with β-Phthalimidonitroethene.
Organic letters, 2015, 17, 4988-4991
1555324 CIFC51 H53 Cl2 N5 O3P 1 21/c 111.813; 18.382; 21.241
90; 92.944; 90
4606Tian, Yaming; Tian, Lumin; He, Xiang; Li, Chunju; Jia, Xueshun; Li, Jian
Indium(III) Chloride-Catalyzed Isocyanide Insertion Reaction to Construct Complex Spirooxindole.
Organic letters, 2015, 17, 4874-4877
1555325 CIFC17 H31 SiP -16.5951; 11.238; 12.03
105.996; 93.545; 94.888
850.6Sabbasani, Venkata R.; Lee, Daesung
Oxidative Dimerization of Silylallenes via Activation of the Allenic C(sp(2))-H Bond Catalyzed by Copper(I) Chloride and N-Hydroxyphthalimide.
Organic letters, 2015, 17, 4878-4881
1555326 CIFC13 H23 SiP -16.2702; 10.955; 11.088
75.965; 74.11; 74.699
694.6Sabbasani, Venkata R.; Lee, Daesung
Oxidative Dimerization of Silylallenes via Activation of the Allenic C(sp(2))-H Bond Catalyzed by Copper(I) Chloride and N-Hydroxyphthalimide.
Organic letters, 2015, 17, 4878-4881
1555327 CIFC15 H10 Cl F2 NP 1 21/n 16.5538; 13.9376; 13.754
90; 92.544; 90
1255.11Aikawa, Kohsuke; Maruyama, Kenichi; Honda, Kazuya; Mikami, Koichi
α-Difluoromethylation on sp(3) Carbon of Nitriles Using Fluoroform and Ruppert-Prakash Reagent.
Organic letters, 2015, 17, 4882-4885
1555328 CIFC35 H30 Br F N4 O4P 18.4125; 9.7659; 11.5692
108.577; 95.876; 110.228
820.9Bao, Xiaoze; Wang, Baomin; Cui, Longchen; Zhu, Guodong; He, Yuli; Qu, Jingping; Song, Yuming
An Organocatalytic Asymmetric Friedel-Crafts Addition/Fluorination Sequence: Construction of Oxindole-Pyrazolone Conjugates Bearing Vicinal Tetrasubstituted Stereocenters.
Organic letters, 2015, 17, 5168-5171
1555329 CIFC17 H13 Cl O2F d d 224.4402; 52.631; 4.31801
90; 90; 90
5554.3Suzuki, Takeyuki; Ismiyarto, ?; Ishizaka, Yuka; Zhou, Da-Yang; Asano, Kaori; Sasai, Hiroaki
One-Pot Catalysis Using a Chiral Iridium Complex/Brønsted Base: Catalytic Asymmetric Synthesis of Catalponol.
Organic letters, 2015, 17, 5176-5179
1555330 CIFC21 H15 F3 N2P 1 21/c 119.794; 11.828; 7.3236
90; 91.476; 90
1714.1Tang, Mi; Tong, Lingfeng; Ju, Lei; Zhai, Wanwan; Hu, Yang; Yu, Xinhong
Benzoic Acid Catalyzed Annulations of α-Amino Acids and Aromatic Aldehydes Containing an ortho-Michael Acceptor: Access to 2,5-Dihydro-1H-benzo[c]azepines and 10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a]azepines.
Organic letters, 2015, 17, 5180-5183
1555331 CIFC18 H22 N2 O2P 1 21/c 18.34; 25.16; 8.134
90; 109.63; 90
1608Yuan, Jingwen; Zhang, Qian; Yu, Mangfei; Huang, Peng; Zhang, Rui; Dong, Dewen
Phenyliodine(III) Diacetate Mediated Oxidative Cyclization of 1-Alkenoyl-1-carbamoyl Cycloalkanes: Access to Spiro-Fused Dihydrofuran-3(2H)-ones.
Organic letters, 2015, 17, 5012-5015
1555332 CIFC24 H15 F2 N O2P -18.126; 9.511; 12.21
84.646; 78.696; 74.768
892Chen, Qi; Chen, Hao; Meng, Xiao; Ma, Yuguo
Lewis Acid Assisted Diels-Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing.
Organic letters, 2015, 17, 5016-5019
1555333 CIFC44 H36 F4 N2 O4 Si2P 1 21/c 16.2172; 11.8634; 29.226
90; 94.257; 90
2149.7Chen, Qi; Chen, Hao; Meng, Xiao; Ma, Yuguo
Lewis Acid Assisted Diels-Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing.
Organic letters, 2015, 17, 5016-5019
1555334 CIFC34 H20 F4 N2 O4P 1 21/c 117.755; 9.629; 15.724
90; 99.347; 90
2652.5Chen, Qi; Chen, Hao; Meng, Xiao; Ma, Yuguo
Lewis Acid Assisted Diels-Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing.
Organic letters, 2015, 17, 5016-5019
1555335 CIFC51 H46 F12 N6 Ni O16 S4P 1 21 113.6455; 18.1359; 24.9551
90; 104.465; 90
5979.9Takeda, Takuya; Harada, Shinji; Nishida, Atsushi
Catalytic Asymmetric Nazarov Cyclization of Heteroaryl Vinyl Ketones through a Crystallographically Defined Chiral Dinuclear Nickel Complex.
Organic letters, 2015, 17, 5184-5187
1555336 CIFC26 H18 Br N O2P 1 21/n 110.612; 16.848; 23.394
90; 96.68; 90
4154.2Liang, Ling; Li, Erqing; Dong, Xuelin; Huang, You
DABCO-Mediated [4 + 4]-Domino Annulation: Access to Functionalized Eight-Membered Cyclic Ethers.
Organic letters, 2015, 17, 4914-4917
1555337 CIFC17 H20 O3P 1 21 18.3018; 14.7835; 12.3636
90; 101.126; 90
1488.86Liao, 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
1555338 CIFC17 H20 O3P -18.0539; 9.0826; 9.9175
102.862; 97.071; 96.384
694.648Liao, 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
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
1555340 CIFC81 H22 O S2C 1 2/c 145.917; 10.214; 19.5587
90; 104.361; 90
8886.3Chen, Si; Li, Zong-Jun; Li, Shu-Hui; Gao, Xiang
Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones.
Organic letters, 2015, 17, 5192-5195
1555341 CIFC79 H22 OP -19.9134; 14.8425; 17.0648
67.983; 89.643; 77.467
2264.5Chen, Si; Li, Zong-Jun; Li, Shu-Hui; Gao, Xiang
Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones.
Organic letters, 2015, 17, 5192-5195
1555342 CIFC80 H24 OP 1 21/c 114.971; 17.4948; 16.7353
90; 107.46; 90
4181.3Chen, Si; Li, Zong-Jun; Li, Shu-Hui; Gao, Xiang
Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones.
Organic letters, 2015, 17, 5192-5195
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
1555345 CIFC15 H19 N O3P 1 21 15.8171; 7.1215; 16.2736
90; 94.53; 90
672.05Wright, 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
1555346 CIFC9 H15 N O2P 1 21 16.1254; 6.9441; 10.8047
90; 102.426; 90
448.82Wright, 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
1555348 CIFC13 H13 N O3P 1 21 18.236; 6.3687; 10.9331
90; 92.94; 90
572.71Wright, 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
1555349 CIFC24 H40 O8P 1 21 17.32024; 8.9338; 17.2413
90; 91.3123; 90
1127.24Wu, Ping; Xue, Jinghua; Yao, Lei; Xu, Liangxiong; Li, Hanxiang; Wei, Xiaoyi
Bisacremines E-G, Three Polycyclic Dimeric Acremines Produced by Acremonium persicinum SC0105.
Organic letters, 2015, 17, 4922-4925
1555350 CIFC25 H25 N O9P -110.925; 10.939; 11.295
113.793; 97.632; 99.629
1187.3Shu, Wen-Ming; Zheng, Kai-Lu; Ma, Jun-Rui; Wu, An-Xin
Transition-Metal-Free Multicomponent Benzannulation Reactions for the Construction of Polysubstituted Benzene Derivatives.
Organic letters, 2015, 17, 5216-5219
1555351 CIFC25 H22 O6P -110.167; 11.5366; 11.951
68.165; 67.543; 79.903
1201.6Shu, Wen-Ming; Zheng, Kai-Lu; Ma, Jun-Rui; Wu, An-Xin
Transition-Metal-Free Multicomponent Benzannulation Reactions for the Construction of Polysubstituted Benzene Derivatives.
Organic letters, 2015, 17, 5216-5219
1555352 CIFC24 H20 O2P 1 21/c 110.2764; 23.0983; 7.47
90; 101.197; 90
1739.4Siyang, Hai Xiao; Ji, Xiao Yue; Wu, Xu Rui; Wu, Xin Yan; Liu, Pei Nian
Lewis Acid Catalyzed Tandem Polycyclization of Internal Alkynols and Vinyl Azides.
Organic letters, 2015, 17, 5220-5223
1555353 CIFC21 H24 Br N OP -18.3568; 9.126; 13.2967
72.212; 72.822; 85.148
922.49Wong, Ying-Chieh; Ke, Zhihai; Yeung, Ying-Yeung
Lewis Basic Sulfide Catalyzed Electrophilic Bromocyclization of Cyclopropylmethyl Amide.
Organic letters, 2015, 17, 4944-4947
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
1555356 CIFC98 H156 Cd4 Cl14 Lu2 N56 O62P n m a35.112; 12.3662; 19.6459
90; 90; 90
8530.3Zhao, Wen-Xuan; Wang, Chuan-Zeng; Chen, Li-Xia; Cong, Hang; Xiao, Xin; Zhang, Yun-Qian; Xue, Sai-Feng; Huang, Ying; Tao, Zhu; Zhu, Qian-Jiang
A Hemimethyl-Substituted Cucurbit[7]uril Derived from 3α-Methyl-glycoluril.
Organic letters, 2015, 17, 5072-5075
1555357 CIFC21 H16 F2 OP -18.2834; 10.8217; 18.382
78.708; 82.706; 89.789
1602.4Yang, Chao; Xu, Zheng-Liang; Shao, Hui; Mou, Xue-Qing; Wang, Jie; Wang, Shao-Hua
A Tin(IV) Chloride Promoted Tandem C-O Bond Cleavage/Nazarov Cyclization/Nucleophilic Addition Reaction of 1,1-Disubstituted Allylic Ethers toward the Synthesis of Multisubstituted Indenes.
Organic letters, 2015, 17, 5288-5291
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
1555359 CIFC19 H23 F2 N O3P 1 21 112.3361; 6.0532; 13.2095
90; 115.922; 90
887.15Aikawa, Kohsuke; Yoshida, Seiya; Kondo, Daisuke; Asai, Yuya; Mikami, Koichi
Catalytic Asymmetric Synthesis of Tertiary Alcohols and Oxetenes Bearing a Difluoromethyl Group.
Organic letters, 2015, 17, 5108-5111
1555360 CIFC38 H30 N2 O4 S2P -19.37; 12.582; 14.702
90.83; 105.888; 110.831
1546Dhiman, Seema; Ramasastry, S. S. V.
One-Pot Relay Gold(I) and Brønsted Acid Catalysis: Cyclopenta[b]annulation of Indoles via Hydroamination/Nazarov-Type Cyclization Cascade of Enynols.
Organic letters, 2015, 17, 5116-5119
1555361 CIFC60 H60 Cl2 N4 O4 RuP -112.0889; 12.4331; 18.0531
75.323; 86.447; 89.594
2619.7Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro
Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.
Organic letters, 2015, 17, 5284-5287
1555362 CIFC22 H24 N2 O4 SP 1 21/c 115.928; 11.573; 11.95
90; 107.075; 90
2105.7Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro
Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.
Organic letters, 2015, 17, 5284-5287
1555363 CIFC24 H23 N O2 SP 1 21/c 116.4534; 8.1341; 16.6107
90; 116.278; 90
1993.3Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro
Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.
Organic letters, 2015, 17, 5284-5287
1555364 CIFC22 H25 N O2 SP -18.1967; 9.0717; 15.216
87.208; 82.37; 65.005
1016.4Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro
Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.
Organic letters, 2015, 17, 5284-5287
1555365 CIFC24 H25 Br N2 O4 SC 1 2 19.512; 19.054; 30.838
90; 93.81; 90
5577Shu, Xing-zhong; Schienebeck, Casi M.; Li, Xiaoxun; Zhou, Xin; Song, Wangze; Chen, Lianqing; Guzei, Ilia A.; Tang, Weiping
Rhodium-Catalyzed Stereoselective Intramolecular [5 + 2] Cycloaddition of 3-Acyloxy 1,4-Enyne and Alkene.
Organic letters, 2015, 17, 5128-5131
1555366 CIFC19 H20 N2 O3P 1 21/c 112.4342; 16.375; 8.6369
90; 106.914; 90
1682.49Sar, Dinabandhu; Bag, Raghunath; Yashmeen, Afsana; Bag, Subhendu Sekhar; Punniyamurthy, Tharmalingam
Synthesis of Functionalized Pyrazoles via Vanadium-Catalyzed C-N Dehydrogenative Cross-Coupling and Fluorescence Switch-On Sensing of BSA Protein.
Organic letters, 2015, 17, 5308-5311
1555367 CIFC18 H23 N O7P 6510.2093; 10.2093; 30.4222
90; 90; 120
2746.08N V G, Moorthy; Dyapa, Rajendar; Pansare, Sunil V.
Formal Synthesis of (+)-Lasubine II and (-)-Subcosine II via Organocatalytic Michael Addition of a Ketone to an α-Nitrostyrene.
Organic letters, 2015, 17, 5312-5315
1555368 CIFC19 H21 N2 O2.5P 1 21 19.5014; 17.2076; 9.9401
90; 90.682; 90
1625.1Palazzo, Teresa A.; Patra, Digambara; Yang, Joung S.; El Khoury, Elsy; Appleton, Mackenzie G.; Haddadin, Makhluf J.; Tantillo, Dean J.; Kurth, Mark J.
Dibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies.
Organic letters, 2015, 17, 5732-5735
1555369 CIFC42 H46 N4 O5P 1 21/c 121.8506; 6.802; 25.1773
90; 113.248; 90
3438.21Palazzo, Teresa A.; Patra, Digambara; Yang, Joung S.; El Khoury, Elsy; Appleton, Mackenzie G.; Haddadin, Makhluf J.; Tantillo, Dean J.; Kurth, Mark J.
Dibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies.
Organic letters, 2015, 17, 5732-5735
1555370 CIFC19 H16 O5P 1 21 17.0727; 8.9761; 11.4306
90; 96.806; 90
720.56Yang, Chunfang; Huang, Chunshuai; Zhang, Wenjun; Zhu, Yiguang; Zhang, Changsheng
Heterologous Expression of Fluostatin Gene Cluster Leads to a Bioactive Heterodimer.
Organic letters, 2015, 17, 5324-5327
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
1555373 CIFC16 H13 N O2 SP 4310.7582; 10.7582; 11.4283
90; 90; 90
1322.7Osborne, 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
1555377 CIFC24 H24 F3 N O4C 1 2/c 128.0198; 9.2681; 17.0333
90; 104.376; 90
4284.9Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555378 CIFC21 H21 N2 O4P -19.5002; 9.6957; 10.3129
96.467; 104.739; 98.162
898.32Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555379 CIFC23 H20 F3 N3 OP 1 21/c 113.6453; 9.9432; 14.4487
90; 91.039; 90
1960Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555380 CIFC22 H27 N3 OC 1 2/c 132.003; 7.0392; 19.0154
90; 120.399; 90
3694.8Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555381 CIFC22 H20 N2 O5P c c n22.182; 22.337; 14.877
90; 90; 90
7371Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555382 CIFC24 H22 N2 OP 1 21/c 117.6141; 8.5636; 12.8104
90; 107.202; 90
1845.89Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555383 CIFC25 H24 N2 O2P 1 21/c 117.188; 9.172; 13.025
90; 108.831; 90
1943.5Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555384 CIFC30 H32 B2 F4 N4P 1 2/c 112.718; 8.6639; 12.342
90; 101.101; 90
1334.5Wang, Jun; Wu, Qinghua; Wang, Shaowu; Yu, Changjiang; Li, Jin; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Conformation-Restricted Partially and Fully Fused BODIPY Dimers as Highly Stable Near-Infrared Fluorescent Dyes.
Organic letters, 2015, 17, 5360-5363
1555385 CIFC30 H34 B2 F4 N4P 1 21/n 117.6404; 8.5702; 20.1377
90; 114.568; 90
2768.8Wang, Jun; Wu, Qinghua; Wang, Shaowu; Yu, Changjiang; Li, Jin; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Conformation-Restricted Partially and Fully Fused BODIPY Dimers as Highly Stable Near-Infrared Fluorescent Dyes.
Organic letters, 2015, 17, 5360-5363
1555386 CIFC25 H24 N4 O4P n a 218.7914; 22.2498; 11.9566
90; 90; 90
2338.79Chingle, Ramesh; Lubell, William D.
Azopeptides: Synthesis and Pericyclic Chemistry.
Organic letters, 2015, 17, 5400-5403
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
1555388 CIFC34 H34 N4 O4P 1 21 110.2983; 10.6899; 13.1072
90; 94.794; 90
1437.89Chingle, Ramesh; Lubell, William D.
Azopeptides: Synthesis and Pericyclic Chemistry.
Organic letters, 2015, 17, 5400-5403
1555389 CIFC29 H25 Br N2 O3P b c a12.7295; 15.5318; 24.571
90; 90; 90
4858Li, Falin; Chen, Jiangfei; Hou, Yading; Li, Yujie; Wu, Xin-Yan; Tong, Xiaofeng
1,3-Dipolar Cycloadditions of 4-Acetoxy Allenoates: Access to 2,3-Dihydropyrazoles, 2,3-Dihydroisoxazoles, and Indolizines.
Organic letters, 2015, 17, 5376-5379
1555390 CIFC23 H25 N S2P 1 21/c 17.4977; 11.606; 23.037
90; 91.639; 90
2003.8Yamauchi, Takayuki; Shibahara, Fumitoshi; Murai, Toshiaki
Direct C-H Bond Arylation of Thienyl Thioamides Catalyzed by Pd-Phenanthroline Complexes.
Organic letters, 2015, 17, 5392-5395
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
1555392 CIFC54.5 H73 Cl5 I2 N8P n m a16.4441; 19.3772; 19.7044
90; 90; 90
6278.62Tepper, 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
1555393 CIFC37 H35 I2 N7C 1 2/c 150.2116; 8.9517; 25.5239
90; 111.754; 90
10655.4Tepper, 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
1555394 CIFC91 H108 Cl3 I4 N15 O4P 1 21/c 120.9995; 15.2694; 28.6315
90; 90.725; 90
9179.9Tepper, 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
1555395 CIFC37 H35 I2 N7 O2P 1 21/c 117.3106; 15.673; 15.0038
90; 109.469; 90
3837.91Tepper, 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
1555397 CIFC62 H73.33 N13 O12R -3 :H20.9278; 20.9278; 11.7428
90; 90; 120
4454Ren, Changliang; Shen, Jie; Zeng, Huaqiang
One-Pot Synthesis of Strained Macrocyclic Pyridone Hexamers and Their High Selectivity toward Cu(2+) Recognition.
Organic letters, 2015, 17, 5946-5949
1555398 CIFC19 H26 O2P 1 21 17.2207; 10.6225; 10.6751
90; 101.193; 90
803.23Weber, 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
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
1555401 CIFC19 H23 N O2P 1 21 17.5354; 8.5029; 11.9989
90; 90.259; 90
768.79Weber, 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
1555402 CIFC22 H15 Cl OP -16.5461; 8.998; 14.2101
92.224; 101.253; 92.809
818.92Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy
Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.
Organic letters, 2015, 17, 5448-5451
1555403 CIFC22 H15 Br OP 1 21/c 16.253; 15.418; 17.593
90; 92.18; 90
1694.9Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy
Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.
Organic letters, 2015, 17, 5448-5451

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