Crystallography Open Database

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1518687 CIFC63 H70 N4 O16P -111.12; 14.029; 20.02
108.726; 98.537; 94.981
2894.8Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518712 CIFC21 H28 O3P 21 21 216.0078; 15.1366; 20.0221
90; 90; 90
1820.76Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518713 CIFC23 H27 F3 O3P 21 21 216.2097; 14.9142; 23.193
90; 90; 90
2147.97Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518718 CIFC18 H26 O4 SiP b c a16.759; 7.4334; 30.141
90; 90; 90
3754.9Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793
1518719 CIFC18 H26 O4 SiP -16.1239; 16.8945; 17.8873
91.468; 95.3024; 90.184
1842.1Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793
1518723 CIFC32 H28 O4 SiP -17.0418; 10.4998; 17.4226
93.591; 96.204; 103.663
1239.21Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.
Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.
Organic letters, 2015, 17, 856-859
1518724 CIFC31 H28 O4 SiP 1 21/n 114.0146; 10.5314; 16.6752
90; 100.775; 90
2417.8Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.
Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.
Organic letters, 2015, 17, 856-859
1518725 CIFC18 H12 F N O3P 1 21/c 13.798; 11.416; 31.2
90; 90.82; 90
1353Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei
One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.
Organic letters, 2015, 17, 1090-1093
1518726 CIFC22 H16 F4 O3P -17.668; 11.45; 11.497
97.96; 98.584; 103.944
952.6Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei
One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.
Organic letters, 2015, 17, 1090-1093
1518747 CIFC14 H9 Cl N4 O2P -111.31; 13.792; 13.982
93.902; 90.56; 112.233
2012.7Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan
Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.
Organic letters, 2015, 17, 1118-1121
1518748 CIFC15 H11 Br N4 O2P b c a10.784; 9.6655; 28.858
90; 90; 90
3007.9Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan
Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.
Organic letters, 2015, 17, 1118-1121
1518770 CIFC20 H16 Cl4 N2P b c a11.2813; 14.1148; 24.5832
90; 90; 90
3914.5Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng
Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.
Organic letters, 2015, 17, 1026-1029
1518771 CIFC18 H26 Cl2 N2P -19.3474; 9.8657; 12.3923
66.695; 69.579; 62.115
908.59Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng
Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.
Organic letters, 2015, 17, 1026-1029
1518772 CIFC28 H23 Br Cl3 N O2P 21 21 219.6557; 10.7366; 25.0366
90; 90; 90
2595.53Saha, Satyajit; Schneider, Christoph
Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.
Organic letters, 2015, 17, 648-651
1518773 CIFC26 H21 N O2 SP 21 21 217.3516; 9.5635; 29.4896
90; 90; 90
2073.33Saha, Satyajit; Schneider, Christoph
Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.
Organic letters, 2015, 17, 648-651
1518783 CIFC23 H16 N2P 1 21/c 114.9264; 8.5389; 13.3223
90; 96.518; 90
1687.02Zhang, Wei; Wei, Jun; Fu, Shaomin; Lin, Dongen; Jiang, Huanfeng; Zeng, Wei
Highly Stereoselective Ruthenium(II)-Catalyzed Direct C2-syn-Alkenylation of Indoles with Alkynes.
Organic letters, 2015, 17, 1349-1352
1518820 CIFC23 H17 N OP 19.9575; 10.7208; 16.4862
91.531; 105.749; 104.208
1633.82Yang, Xiao-Fei; Hu, Xu-Hong; Loh, Teck-Peng
Expedient Synthesis of Pyrroloquinolinones by Rh-Catalyzed Annulation of N-Carbamoyl Indolines with Alkynes through a Directed C-H Functionalization/C-N Cleavage Sequence.
Organic letters, 2015, 17, 1481-1484
1518842 CIFC15 H13 F O2 SP 21 21 215.9536; 7.269; 31.978
90; 90; 90
1383.9Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang
Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.
Organic letters, 2015, 17, 1692-1695
1518936 CIFC18 H24 F N O4 SP 1 21/c 19.8882; 17.552; 11.4151
90; 103.067; 90
1929.9Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518937 CIFC13 H15 N O4 SP -16.7205; 8.781; 11.3856
103.22; 104.242; 92.033
630.98Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518938 CIFC19 H28 N2 O4 SP -110.0063; 10.3287; 10.8385
65.843; 70.701; 84.706
963.4Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518939 CIFC15 H18 N2 SP 1 21/c 110.8363; 14.406; 9.9733
90; 117.4; 90
1382.2Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518940 CIFC15 H21 N O3 SP 1 21/c 17.3226; 10.563; 18.9019
90; 92.929; 90
1460.13Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518941 CIFC14 H19 N O3 SP b c a8.4818; 10.9461; 30.035
90; 90; 90
2788.5Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518989 CIFC19 H12 Cl2 N2P 1 21/c 112.7382; 11.0562; 12.4976
90; 112.701; 90
1623.76Tiwari, Virendra Kumar; Kamal, Neha; Kapur, Manmohan
Ruthenium-catalyzed heteroatom-directed regioselective C-h arylation of indoles using a removable tether.
Organic letters, 2015, 17, 1766-1769
1518990 CIFC17 H17 O P SiP c a 2114.4427; 6.5207; 16.6673
90; 90; 90
1569.67Xu, Youzhi; Wang, Zhihua; Gan, Zhenjie; Xi, Qiuzhen; Duan, Zheng; Mathey, François
Versatile synthesis of phospholides from open-chain precursors. Application to annelated pyrrole- and silole-phosphole rings.
Organic letters, 2015, 17, 1732-1734
1518991 CIFC21 H17 F O2 SP 1 21/n 112.402; 5.782; 24.377
90; 100.253; 90
1720.1Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang
Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.
Organic letters, 2015, 17, 1692-1695
1518992 CIFC16 H16 O2 SP 21 21 215.7471; 8.0541; 31.351
90; 90; 90
1451.2Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang
Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.
Organic letters, 2015, 17, 1692-1695
1518993 CIFC21 H18 O2 SP 1 21/n 112.3084; 5.8277; 24.345
90; 100.373; 90
1717.7Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang
Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.
Organic letters, 2015, 17, 1692-1695
1518994 CIFC14 H17 N O3 SC 1 2/c 125.7457; 5.8011; 19.0494
90; 98.23; 90
2815.79Cheng, Cungui; Liu, Shuiyou; Zhu, Gangguo
Palladium-catalyzed cycloisomerization and aerobic oxidative cycloisomerization of homoallenyl amides: a facile and divergent approach to 2-aminofurans.
Organic letters, 2015, 17, 1581-1584
1518995 CIFC15 H21 N O4 SP b c n16.428; 13.329; 14.387
90; 90; 90
3150Zhu, Haitao; Chen, Pinhong; Liu, Guosheng
Palladium-catalyzed intramolecular aminoacetoxylation of unactivated alkenes with hydrogen peroxide as oxidant.
Organic letters, 2015, 17, 1485-1488
1518996 CIFC20 H20 N2 O3P 21 21 219.8991; 10.1513; 17.5003
90; 90; 90
1758.6Yetra, Santhivardhana Reddy; Mondal, Santigopal; Suresh, Eringathodi; Biju, Akkattu T.
Enantioselective Synthesis of Functionalized Pyrazoles by NHC-Catalyzed Reaction of Pyrazolones with α,β-Unsaturated Aldehydes.
Organic letters, 2015, 17, 1417-1420
1518997 CIFC11 H14 O3P n a 2114.5121; 5.9558; 24.1332
90; 90; 90
2085.9Qin, Yan; Zhang, Long; Lv, Jian; Luo, Sanzhong; Cheng, Jin-Pei
Bioinspired Organocatalytic Aerobic C-H Oxidation of Amines with an ortho-Quinone Catalyst.
Organic letters, 2015, 17, 1469-1472
1518998 CIFC16 H14 O2P 21 21 218.477; 8.5847; 17.547
90; 90; 90
1276.94Jiang, Liyin; Jia, Tao; Wang, Min; Liao, Jian; Cao, Peng
Pd-catalyzed enantioselective hydroalkoxylation of alkoxyallenes with phenol for construction of acyclic o,o-acetals.
Organic letters, 2015, 17, 1070-1073
1518999 CIFC17 H13 F O3 SP 1 21/n 19.2698; 11.0134; 15.0573
90; 105.111; 90
1484.08Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Bi(OTf)3-Mediated Cycloisomerization of γ-Alkynyl Arylketones: Application to the Synthesis of Substituted Furans.
Organic letters, 2015, 17, 1264-1267
1519496 CIFC22 H20 Br NP 16.134; 7.123; 10.777
102.328; 106.299; 90.659
440.2Zhang, Zhenhua; Du, Haifeng
Cis-selective and highly enantioselective hydrogenation of 2,3,4-trisubstituted quinolines.
Organic letters, 2015, 17, 2816-2819
1519622 CIFC22 H18 Cl N O3 PdP 1 21/c 119.306; 4.5687; 22.128
90; 103.674; 90
1896.4Ren, Zhi; Schulz, Jonathan E.; Dong, Guangbin
Catalytic Ortho-Acetoxylation of Masked Benzyl Alcohols via an Exo-Directing Mode.
Organic letters, 2015, 17, 2696-2699
1519623 CIFC15 H10 I N O2C 1 c 124.877; 7.087; 7.92
90; 90.593; 90
1396.2Huang, Hai; Zhu, Xiaolin; He, Guangke; Liu, Qi; Fan, Junzhen; Zhu, Hongjun
Controlled Synthesis of 1,3,5-Oxadiazin-2-ones and Oxazolones through Regioselective Iodocyclization of Ynamides.
Organic letters, 2015, 17, 2510-2513
1519625 CIFC32 H30 B NP 1 21/c 110.2671; 10.1236; 23.3329
90; 98.876; 90
2396.18Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning
One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.
Organic letters, 2015, 17, 2486-2489
1519626 CIFC32 H32 B NP 1 21/c 110.0993; 10.2609; 23.8794
90; 97.3582; 90
2454.19Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning
One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.
Organic letters, 2015, 17, 2486-2489
1519627 CIFC38 H34 B NP -18.8087; 11.1753; 16.1219
72.148; 78.052; 74.662
1443.04Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning
One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.
Organic letters, 2015, 17, 2486-2489
1519628 CIFC102 H70 B4 O20C 1 2/c 130.624; 56.38; 22.177
90; 93.399; 90
38223Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Multilayered inclusion nanocycles of anionic spiroborates.
Organic letters, 2015, 17, 2466-2469
1519629 CIFC21 H26 N2 O2 SP 1 21/c 17.3915; 13.779; 19.135
90; 93.863; 90
1944.4Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar
Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.
Organic letters, 2015, 17, 2226-2229
1519630 CIFC16 H14 N2 O2 SP 1 21/c 111.225; 13.361; 11.0143
90; 118.102; 90
1457.2Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar
Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.
Organic letters, 2015, 17, 2226-2229
1519631 CIFC17 H16 N2 O2 SP 1 21/c 18.9148; 16.7339; 10.5655
90; 95.855; 90
1567.93Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar
Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.
Organic letters, 2015, 17, 2226-2229
1519651 CIFC14 H15 F3 O4 SP 1 21/n 15.4571; 34.89; 7.6271
90; 96.378; 90
1443.2Liu, Yafei; Shao, Xinxin; Zhang, Panpan; Lu, Long; Shen, Qilong
Trifluoromethyl-substituted sulfonium ylide: rh-catalyzed carbenoid addition to trifluoromethylthioether.
Organic letters, 2015, 17, 2752-2755
1519652 CIFC47 H59 N O5P n 21 a18.4589; 58.006; 11.59672
90; 90; 90
12416.9Slavík, Petr; Eigner, Václav; Lhoták, Pavel
Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.
Organic letters, 2015, 17, 2788-2791
1519653 CIFC41 H46 O5C 1 2/c 134.9361; 10.48642; 26.842
90; 135.583; 90
6882.4Slavík, Petr; Eigner, Václav; Lhoták, Pavel
Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.
Organic letters, 2015, 17, 2788-2791
1519654 CIFC48.5 H58 O6.5P 1 21 120.7243; 10.45113; 21.5504
90; 113.543; 90
4279.1Slavík, Petr; Eigner, Václav; Lhoták, Pavel
Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.
Organic letters, 2015, 17, 2788-2791
1519655 CIFC20 H16 Br N O4C 1 c 114.0307; 8.5721; 15.203
90; 109.89; 90
1719.4Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin
Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air.
Organic letters, 2015, 17, 2684-2687
1519656 CIFC25 H20 N2 O2P 1 21/c 113.373; 16.581; 8.8083
90; 93.638; 90
1949.2Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin
Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air.
Organic letters, 2015, 17, 2684-2687
1519657 CIFC24 H28 Cl N O7P 1 21/n 110.5446; 9.5462; 24.575
90; 91.778; 90
2472.5Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong
Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones.
Organic letters, 2015, 17, 2680-2683
1519658 CIFC28 H28 Br N O6P 21 21 2110.409; 15.4718; 16.588
90; 90; 90
2671.4Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong
Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones.
Organic letters, 2015, 17, 2680-2683
1519694 CIFC14 H11 N O4 SP 1 21/c 15.7372; 21.0648; 10.9631
90; 94.428; 90
1321Singh, Rahul; Allam, Bharat Kumar; Singh, Neetu; Kumari, Kumkum; Singh, Satish Kumar; Singh, Krishna Nand
A Direct Metal-Free Decarboxylative Sulfono Functionalization (DSF) of Cinnamic Acids to α,β-Unsaturated Phenyl Sulfones.
Organic letters, 2015, 17, 2656-2659
1519695 CIFC23 H22 O2P 21 21 218.099; 13.445; 16.407
90; 90; 90
1786.6Mitra, Nirmal K.; Meudom, Rolande; Gorden, John D.; Merner, Bradley L.
A non-cross-coupling approach to arene-bridged macrocycles: synthesis, structure, and direct, regioselective functionalization of a cycloparaphenylene fragment.
Organic letters, 2015, 17, 2700-2703
1519696 CIFC13 H13 F OP 21 21 216.1061; 18.8064; 27.8827
90; 90; 90
3201.88Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519697 CIFC9 H10 Br F OP 1 21 18.013; 5.1662; 10.972
90; 93.376; 90
453.4Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519698 CIFC10 H13 F OP 21 21 215.5342; 11.1421; 14.6505
90; 90; 90
903.39Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519755 CIFC15 H16 O4P 1 21/c 17.4665; 21.583; 8.4033
90; 107.586; 90
1290.9Zhang, Xuxue; Dai, Wenpeng; Wu, Wei; Cao, Song
Copper-Catalyzed Coupling Cyclization of gem-Difluoroalkenes with Activated Methylene Carbonyl Compounds: Facile Domino Access to Polysubstituted Furans.
Organic letters, 2015, 17, 2708-2711
1519756 CIFC30 H42 O5P 1 21 17.3312; 12.6193; 14.4778
90; 98.847; 90
1323.47Zhao, Qian-Qian; Song, Qiu-Yan; Jiang, Kan; Li, Guang-Da; Wei, Wen-Jun; Li, Ya; Gao, Kun
Spirochensilides A and B, Two New Rearranged Triterpenoids from Abies chensiensis.
Organic letters, 2015, 17, 2760-2763
1519757 CIFC10 H7 Br Cl2 N2 OP b c a12.6226; 12.3709; 14.1124
90; 90; 90
2203.7Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519758 CIFC12 H12 Br2 N2 OP 1 21/c 17.3945; 20.124; 17.43
90; 91.44; 90
2592.9Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519759 CIFC11 H10 Br2 N2P 1 21/c 114.9133; 10.5056; 7.3297
90; 103.561; 90
1116.35Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519760 CIFC11 H7 Cl2 F3 N2 O1.5P 1 21/c 17.501; 40.025; 16.7795
90; 94.664; 90
5021Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519761 CIFC11 H9 Br2 F N2P b c a14.443; 7.5861; 21.306
90; 90; 90
2334.4Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519848 CIFC12 H14 O3P 1 21/c 18.8887; 18.4179; 6.9957
90; 115.638; 90
1032.52Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo
Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.
Organic letters, 2015, 17, 2672-2675
1519849 CIFC12 H14 O3P 1 21/c 110.7308; 8.7467; 12.089
90; 109.485; 90
1069.68Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo
Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.
Organic letters, 2015, 17, 2672-2675
1519850 CIFC22 H16 Br N O2P 1 21/c 15.7399; 15.532; 20.365
90; 96.93; 90
1802.3Dhanasekaran, Sivasankaran; Kayet, Anirban; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.
Unified Approach to Isoindolinones and THIQs via Lewis Acid Catalyzed Domino Mukaiyama-Mannich Lactamization/Alkylations: Application in the Synthesis of (±)-Homolaudanosine.
Organic letters, 2015, 17, 2780-2783
1519851 CIFC16 H12 N4P 1 21/c 14.8624; 11.167; 23.437
90; 94.33; 90
1269Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Li, Deng-Kui; Wu, An-Xin
Consecutive Cycloaddition/SNAr/Reduction/Cyclization/Oxidation Sequences: A Copper-Catalyzed Multicomponent Synthesis of Fused N-Heterocycles.
Organic letters, 2015, 17, 2820-2823
1519923 CIFC21 H34 O3P 1 21 16.1791; 23.0423; 6.9392
90; 110.037; 90
928.21Hosseini, Abolfazl; Seidel, Daniel; Miska, Andreas; Schreiner, Peter R.
Fluoride-assisted activation of calcium carbide: a simple method for the ethynylation of aldehydes and ketones.
Organic letters, 2015, 17, 2808-2811
1519924 CIFC25 H21 Fe N3P 1 21/c 110.9392; 8.3314; 22.5089
90; 102.759; 90
2000.78Wei, Fang; Li, Haoyu; Song, Chuanling; Ma, Yudao; Zhou, Ling; Tung, Chen-Ho; Xu, Zhenghu
Cu/Pd-Catalyzed, Three-Component Click Reaction of Azide, Alkyne, and Aryl Halide: One-Pot Strategy toward Trisubstituted Triazoles.
Organic letters, 2015, 17, 2860-2863
1519998 CIFC20 H30 N0 O5P 21 21 217.0685; 15.143; 17.388
90; 90; 90
1861.2Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha
Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.
Organic letters, 2015, 17, 2840-2843
1519999 CIFC20 H28 O5P 1 21 19.4777; 7.3392; 13.4089
90; 91.432; 90
932.41Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha
Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.
Organic letters, 2015, 17, 2840-2843
1520000 CIFC29 H36 O8P 1 21/c 113.2416; 13.1779; 15.2428
90; 109.387; 90
2509Fukaya, Keisuke; Kodama, Keisuke; Tanaka, Yuta; Yamazaki, Hirohisa; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 2. Construction of the ABCD Ring and Formal Synthesis.
Organic letters, 2015, 17, 2574-2577
1520001 CIFC54 H46 Co N2 P3P 1 21/n 114.376; 14.699; 21.34
90; 107.79; 90
4293.8Scheuermann, Margaret L.; Johnson, Elizabeth J.; Chirik, Paul J.
Alkene isomerization-hydroboration promoted by phosphine-ligated cobalt catalysts.
Organic letters, 2015, 17, 2716-2719
1520002 CIFC29 H38 O8P 1 21/n 19.3612; 19.6336; 14.1965
90; 101.762; 90
2554.4Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520003 CIF
Paper
C42 H50 O10P -19.6397; 13.6008; 15.0461
83.6966; 77.488; 77.9768
1879.2Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520004 CIFC30.25 H41 O8P -111.3343; 15.4666; 16.487
85.1124; 78.3773; 78.5231
2771.3Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520005 CIFC15 H21 N O2P 1 21/c 18.5353; 10.6984; 15.609
90; 104.429; 90
1380.4Zhou, Wei; Ni, Shengyang; Mei, Haibo; Han, Jianlin; Pan, Yi
Hydroxyalkylation-initiated radical cyclization of N-allylbenzamide for direct construction of isoquinolinone.
Organic letters, 2015, 17, 2724-2727
1520068 CIFC32 H36 Br2 N4 O2P 1 21/c 110.037; 8.2451; 18.991
90; 101.279; 90
1541.3Zhu, Xiaxia; Du, Haifeng
A Highly Stereoselective Metal-Free Hydrogenation of Diimines for the Synthesis of Cis-Vicinal Diamines.
Organic letters, 2015, 17, 3106-3109
1520116 CIFC28 H19 NP -19.0455; 9.563; 11.529
103.716; 98.763; 98.986
938.1Liu, Xingyan; Li, Xiaoyu; Liu, Hu; Guo, Qiang; Lan, Jingbo; Wang, Ruilin; You, Jingsong
Aldehyde as a Traceless Directing Group for Rh(III)-Catalyzed C-H Activation: A Facile Access to Diverse Indolo[1,2-a]quinolines.
Organic letters, 2015, 17, 2936-2939
1520117 CIFC17.5 H18 F8 I O3.5 S2P -18.9435; 12.1892; 12.2642
63.163; 87.526; 77.6
1162.92Matsuzaki, Kohei; Okuyama, Kenta; Tokunaga, Etsuko; Saito, Norimichi; Shiro, Motoo; Shibata, Norio
Synthesis of Diaryliodonium Salts Having Pentafluorosulfanylarenes and Their Application to Electrophilic Pentafluorosulfanylarylation of C-, O-, N-, and S-Nucleophiles.
Organic letters, 2015, 17, 3038-3041
1520220 CIFC24 H19 NC 1 2/c 142.784; 6.0454; 31.552
90; 119.951; 90
7071Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520221 CIFC30 H23 NP 1 21/c 112.0216; 6.2012; 30.083
90; 101.315; 90
2199Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520222 CIFC23 H19 NC 1 2/c 129.558; 6.041; 19.696
90; 104.661; 90
3402.4Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520223 CIFC14 H16 Cl3 N O3P 3216.1172; 16.1172; 5.6393
90; 90; 120
1268.63Skvorcova, Marija; Grigorjeva, Liene; Jirgensons, Aigars
Tetrahydro-1,3-oxazepines via Intramolecular Amination of Cyclopropylmethyl Cation.
Organic letters, 2015, 17, 2902-2904
1520224 CIFC22 H22 N4 O2 SP 1 21 110.363; 9.318; 11.453
90; 112.7; 90
1020.3Wang, Linqing; Yang, Dongxu; Li, Dan; Wang, Rui
Catalytic Enantioselective Ring-Opening and Ring-Closing Reactions of 3-Isothiocyanato Oxindoles and N-(2-Picolinoyl)aziridines.
Organic letters, 2015, 17, 3004-3007
1520225 CIFC13 H21 N3 O3P 1 21/c 14.5905; 23.474; 13.2529
90; 91.746; 90
1427.4Martínez, Luís; Martorell, Gabriel; Sampedro, Ángel; Ballester, Pablo; Costa, Antoni; Rotger, Carmen
Hydrogen Bonded Squaramide-Based Foldable Module Induces Both β- and α-Turns in Hairpin Structures of α-Peptides in Water.
Organic letters, 2015, 17, 2980-2983
1520297 CIFC52 H60 Br N4 O18 S2C 1 2/c 126.6011; 19.037; 14.4208
90; 114.731; 90
6633Carrasco-Ruiz, Anayeli; Tiburcio, Jorge
Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.
Organic letters, 2015, 17, 1858-1861
1520298 CIFC52 H86 N4 O32 S2P 1 21/n 111.8381; 23.4128; 11.8991
90; 107.339; 90
3148.12Carrasco-Ruiz, Anayeli; Tiburcio, Jorge
Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.
Organic letters, 2015, 17, 1858-1861
1520299 CIFC22 H23 I O3P 21 21 215.7232; 10.8546; 32.913
90; 90; 90
2044.7Merad, Jérémy; Borkar, Prashant; Bouyon Yenda, Tracy; Roux, Christèle; Pons, Jean-Marc; Parrain, Jean-Luc; Chuzel, Olivier; Bressy, Cyril
Highly Enantioselective Acylation of Acyclic Meso 1,3-Diols through Synergistic Isothiourea-Catalyzed Desymmetrization/Chiroablative Kinetic Resolution.
Organic letters, 2015, 17, 2118-2121
1520300 CIFC36 H46 N4 O2P -17.1052; 14.1156; 16.3735
105.153; 91.858; 102.309
1541.85Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian
Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.
Organic letters, 2015, 17, 2210-2213
1520301 CIFC41 H58.333 N5 OP 1 21/c 126.0651; 15.2582; 9.5468
90; 96.584; 90
3771.8Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian
Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.
Organic letters, 2015, 17, 2210-2213
1520302 CIFC33 H31 Br2 N O6P 1 21/c 118.4779; 9.1189; 19.3437
90; 109.352; 90
3075.2Tang, Shaojian; Park, Jong Yeun; Yeagley, Andrew A.; Sabat, Michal; Chruma, Jason J.
Decarboxylative Generation of 2-Azaallyl Anions: 2-Iminoalcohols via a Decarboxylative Erlenmeyer Reaction.
Organic letters, 2015, 17, 2042-2045
1520303 CIFC13 H23 Cl N2 NiP 1 21/n 111.1164; 12.6843; 11.5897
90; 118.363; 90
1438.02Shields, Jason D.; Gray, Erin E.; Doyle, Abigail G.
A modular, air-stable nickel precatalyst.
Organic letters, 2015, 17, 2166-2169
1520304 CIFC66.33 H81.67 N2 O4 YbP 21 21 2115.592; 20.5827; 60.065
90; 90; 90
19276.4Zeng, Chao; Yuan, Dan; Zhao, Bei; Yao, Yingming
Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Catalyzed by Rare-Earth Amides [(Me3Si)2N]3RE(μ-Cl)Li(THF)3 with Phenoxy-Functionalized Chiral Prolinols.
Organic letters, 2015, 17, 2242-2245
1520305 CIFC6 H9 N O4C 1 2/c 116.4651; 6.6186; 14.9686
90; 109.033; 90
1542Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520306 CIFC12 H19 N O3P 1 21/c 111.0623; 9.4884; 11.6015
90; 90.961; 90
1217.56Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520307 CIFC10 H16 B F2 N O3P -19.5474; 11.4938; 11.5223
92.227; 96.964; 91.605
1253.45Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520308 CIFC12 H20 B F2 N O3P 1 21/n 17.8638; 14.0418; 12.6427
90; 91.6599; 90
1395.45Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125

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