Crystallography Open Database
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Searching volume of publication is 11
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1504046 | CIF | C16 H25 N O2 S | P 1 c 1 | 6.119; 13.231; 20.15 90; 91.94; 90 | 1630 | Wang, Bing; Wang, Yong-Jun SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism. Organic letters, 2009, 11, 3410-3413 |
1504047 | CIF | C13 H29 N O3 S | P 21 21 21 | 6.252; 14.188; 18.445 90; 90; 90 | 1636.1 | Wang, Bing; Wang, Yong-Jun SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism. Organic letters, 2009, 11, 3410-3413 |
1504048 | CIF | C14 H31 N O3 S | P 21 21 21 | 6.51; 14.258; 18.556 90; 90; 90 | 1722.4 | Wang, Bing; Wang, Yong-Jun SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism. Organic letters, 2009, 11, 3410-3413 |
1504049 | CIF | C42 H42 N6 O5 | C 1 2/c 1 | 24.171; 9.0645; 19.641 90; 123.943; 90 | 3570 | Li, Guo-You; Yang, Tao; Luo, Ying-Gang; Chen, Xiao-Zhen; Fang, Dong-Mei; Zhang, Guo-Lin Brevianamide J, a new indole alkaloid dimer from fungus Aspergillus versicolor. Organic letters, 2009, 11, 3714-3717 |
1504050 | CIF | C18 H15 N3 O3 | P 1 21 1 | 7.912; 7.392; 14.05 90; 104.92; 90 | 794 | Li, Guo-You; Yang, Tao; Luo, Ying-Gang; Chen, Xiao-Zhen; Fang, Dong-Mei; Zhang, Guo-Lin Brevianamide J, a new indole alkaloid dimer from fungus Aspergillus versicolor. Organic letters, 2009, 11, 3714-3717 |
1504051 | CIF | C17 H28 Cl N2 Rh | P 1 21/n 1 | 6.5715; 18.7963; 13.799 90; 94.439; 90 | 1699.3 | Snead, David R.; Ghiviriga, Ion; Abboud, Khalil A.; Hong, Sukwon A new route to acyclic diaminocarbenes via lithium-halogen exchange. Organic letters, 2009, 11, 3274-3277 |
1504052 | CIF | C17 H28 Cl Ir N2 | P 1 21/c 1 | 9.8235; 14.9332; 23.221 90; 91.616; 90 | 3405.1 | Snead, David R.; Ghiviriga, Ion; Abboud, Khalil A.; Hong, Sukwon A new route to acyclic diaminocarbenes via lithium-halogen exchange. Organic letters, 2009, 11, 3274-3277 |
1504053 | CIF | C13 H22 Cl Ir N2 | P 21 21 21 | 7.277; 12.449; 15.738 90; 90; 90 | 1425.7 | Snead, David R.; Ghiviriga, Ion; Abboud, Khalil A.; Hong, Sukwon A new route to acyclic diaminocarbenes via lithium-halogen exchange. Organic letters, 2009, 11, 3274-3277 |
1504054 | CIF | C22 H16 Br N O | P 21 21 21 | 6.195; 7.802; 35.452 90; 90; 90 | 1713.5 | Li, Yi; Shi, Fu-Qiang; He, Qing-Li; You, Shu-Li N-heterocyclic carbene-catalyzed cross-coupling of aldehydes with arylsulfonyl indoles. Organic letters, 2009, 11, 3182-3185 |
1504055 | CIF | C11 H17 N O3 | P -1 | 6.6599; 9.8956; 9.9738 108.604; 96.856; 97.248 | 609.01 | Meyers, Marvin J.; Muizebelt, Inouk; van Wiltenburg, Jim; Brown, David L.; Thorarensen, Atli Synthesis of tert-butyl 6-oxo-2-azaspiro[3.3]heptane-2-carboxylate. Organic letters, 2009, 11, 3523-3525 |
1504056 | CIF | C66 H66 | P 1 21/c 1 | 15.0858; 17.9286; 17.9396 90; 94.962; 90 | 4833.9 | Zhai, Linyi; Shukla, Ruchi; Rathore, Rajendra Oxidative C-C bond formation (Scholl reaction) with DDQ as an efficient and easily recyclable oxidant. Organic letters, 2009, 11, 3474-3477 |
1504057 | CIF | C20 H19 N O4 | P 1 21/c 1 | 6.854; 7.879; 32.765 90; 90; 90 | 1769.4 | Xu, Silong; Zhou, Lili; Zeng, San; Ma, Renqin; Wang, Zhihong; He, Zhengjie Phosphine-mediated olefination between aldehydes and allenes: an efficient synthesis of trisubstituted 1,3-dienes with high E-selectivity. Organic letters, 2009, 11, 3498-3501 |
1504058 | CIF | C16 H17 N O6 | P -1 | 8.2434; 9.3954; 10.116 82.63; 84.66; 80.19 | 763.6 | Xu, Silong; Zhou, Lili; Zeng, San; Ma, Renqin; Wang, Zhihong; He, Zhengjie Phosphine-mediated olefination between aldehydes and allenes: an efficient synthesis of trisubstituted 1,3-dienes with high E-selectivity. Organic letters, 2009, 11, 3498-3501 |
1504059 | CIF | C16 H22 O7 | P 1 21/c 1 | 6.986; 24.324; 18.651 90; 90.932; 90 | 3168.9 | Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position. Organic letters, 2009, 11, 3610-3613 |
1504060 | CIF | C16 H22 O7 | P 1 21/c 1 | 10.367; 10.635; 14.676 90; 100.819; 90 | 1589.3 | Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position. Organic letters, 2009, 11, 3610-3613 |
1504061 | CIF | C19 H22 O4 | P 1 21/c 1 | 10.489; 13.758; 12.54 90; 123.65; 90 | 1506.4 | Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position. Organic letters, 2009, 11, 3610-3613 |
1504062 | CIF | C12 H16 O3 | P 1 21/c 1 | 12.1; 7.3; 12.752 90; 111.89; 90 | 1045.2 | Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position. Organic letters, 2009, 11, 3610-3613 |
1504063 | CIF | C21 H26 O6 | P 1 21/c 1 | 7.724; 27.076; 9.347 90; 100.51; 90 | 1922 | Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position. Organic letters, 2009, 11, 3610-3613 |
1504064 | CIF | C25 H26 Br N O4 | P b c a | 17.103; 8.857; 29.744 90; 90; 90 | 4505.7 | Shintani, Ryo; Hayashi, Shin-ya; Murakami, Masataka; Takeda, Momotaro; Hayashi, Tamio Stereoselective synthesis of spirooxindoles by palladium-catalyzed decarboxylative cyclization of gamma-methylidene-delta-valerolactones with isatins. Organic letters, 2009, 11, 3754-3756 |
1504065 | CIF | C16 H19 N O2 | P 1 21/c 1 | 7.1402; 12.5429; 15.2299 90; 101.104; 90 | 1338.44 | Li, Cheng; Li, Xinyu; Hong, Ran Synthetic study on tetrapetalones: stereoselective cyclization of N-acyliminium ion to construct substituted 1-benzazepines. Organic letters, 2009, 11, 4036-4039 |
1504066 | CIF | C16 H17 N O3 | P 21 21 21 | 7.6034; 12.7414; 13.9945 90; 90; 90 | 1355.76 | Li, Cheng; Li, Xinyu; Hong, Ran Synthetic study on tetrapetalones: stereoselective cyclization of N-acyliminium ion to construct substituted 1-benzazepines. Organic letters, 2009, 11, 4036-4039 |
1504067 | CIF | C24 H25 N O | P 21 21 21 | 6.5177; 15.986; 18.6727 90; 90; 90 | 1945.55 | Concellón, José M; Tuya, Paula; del Solar, Virginia; García-Granda, Santiago; Díaz, M Rosario Efficient and highly selective synthesis of enantiopure cis- or trans-3,4-disubstituted 1,2,3,4-tetrahydroisoquinolines. Organic letters, 2009, 11, 3750-3753 |
1504068 | CIF | C24 H28 O6 S2 | P 1 21/c 1 | 10.3844; 11.1279; 19.5084 90; 98.041; 90 | 2232.2 | Tarselli, Michael A.; Zuccarello, J. Lucas; Lee, Stephen J.; Gagné, Michel R Gold(I)-catalyzed cascade cyclization of allenyl epoxides. Organic letters, 2009, 11, 3490-3492 |
1504069 | CIF | C34 H36 F6 Mn N4 O6 S2 | P 43 21 2 | 15.0588; 15.0588; 15.827 90; 90; 90 | 3589 | Wu, Mei; Wang, Bin; Wang, Shoufeng; Xia, Chungu; Sun, Wei Asymmetric epoxidation of olefins with chiral bioinspired manganese complexes. Organic letters, 2009, 11, 3622-3625 |
1504070 | CIF | C42 H40 F6 Mn N4 O6 S2 | P 21 21 21 | 17.639; 16.204; 16.203 90; 90; 90 | 4631.2 | Wu, Mei; Wang, Bin; Wang, Shoufeng; Xia, Chungu; Sun, Wei Asymmetric epoxidation of olefins with chiral bioinspired manganese complexes. Organic letters, 2009, 11, 3622-3625 |
1504071 | CIF | C17 H22 Br N3 O5 | R 3 :H | 21.619; 21.619; 12.828 90; 90; 120 | 5192.3 | Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun Highly enantioselective and organocatalytic alpha-amination of 2-oxindoles. Organic letters, 2009, 11, 3874-3877 |
1504072 | CIF | C23 H26 Cl N3 O5 | P -1 | 8.9418; 12.02; 12.756 115.51; 92.14; 107.65 | 1156.4 | Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun Highly enantioselective and organocatalytic alpha-amination of 2-oxindoles. Organic letters, 2009, 11, 3874-3877 |
1504073 | CIF | C13 H11 N O S | P 1 21 1 | 5.8503; 8.4929; 10.957 90; 95.88; 90 | 541.55 | Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun Highly enantioselective and organocatalytic alpha-amination of 2-oxindoles. Organic letters, 2009, 11, 3874-3877 |
1504074 | CIF | C33 H24 O | P 21 21 21 | 10.4248; 11.0694; 20.658 90; 90; 90 | 2383.9 | Chen, Yifeng; Lu, Yuhua; Li, Guijie; Liu, Yuanhong Gold-catalyzed cascade Friedel-Crafts/furan-alkyne cycloisomerizations for the highly efficient synthesis of arylated (Z)-enones or -enals. Organic letters, 2009, 11, 3838-3841 |
1504075 | CIF | C16 H18 O2 | P 1 21/c 1 | 9.971; 8.96; 15.88 90; 103.924; 90 | 1377 | Zheng, Zhao-Jing; Shu, Xing-Zhong; Ji, Ke-Gong; Zhao, Shu-Chun; Liang, Yong-Min Acid-catalyzed skeletal rearrangement of epoxy alkynes: a fast access to highly functionalized allenes. Organic letters, 2009, 11, 3214-3217 |
1504076 | CIF | C15 H17 Cl O2 | P 1 21/c 1 | 9.4886; 8.7358; 16.598 90; 95.417; 90 | 1369.7 | Zheng, Zhao-Jing; Shu, Xing-Zhong; Ji, Ke-Gong; Zhao, Shu-Chun; Liang, Yong-Min Acid-catalyzed skeletal rearrangement of epoxy alkynes: a fast access to highly functionalized allenes. Organic letters, 2009, 11, 3214-3217 |
1504077 | CIF | C30 H34 B2 O4 | F d d 2 | 36.848; 45.584; 6.2397 90; 90; 90 | 10481 | Kimoto, Takakazu; Tanaka, Kenro; Sakai, Yoshimasa; Ohno, Akira; Yoza, Kenji; Kobayashi, Kenji 2,8- and 2,9-Diboryltetracenes as useful building blocks for extended pi-conjugated tetracenes. Organic letters, 2009, 11, 3658-3661 |
1504078 | CIF | C26.52 H48.95 N8.26 O13.48 S | C 1 2/c 1 | 21.0704; 8.8723; 20.4017 90; 121.08; 90 | 3266.5 | Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin The influence of amine functionalities on anion binding in polyamide-containing macrocycles. Organic letters, 2009, 11, 3654-3657 |
1504079 | CIF | C26 H54 N8 O18 P2 | P -1 | 8.1169; 11.2001; 11.4236 108.885; 93.062; 107.523 | 923.8 | Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin The influence of amine functionalities on anion binding in polyamide-containing macrocycles. Organic letters, 2009, 11, 3654-3657 |
1504080 | CIF | C32 H60 N8 O13 S | P 1 21/c 1 | 10.753; 20.1934; 17.5334 90; 99.367; 90 | 3756.4 | Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin The influence of amine functionalities on anion binding in polyamide-containing macrocycles. Organic letters, 2009, 11, 3654-3657 |
1504081 | CIF | C35.32 H62.76 N8 O14.77 P | P 1 21/n 1 | 10.4079; 20.877; 20.852 90; 102.5; 90 | 4423.4 | Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin The influence of amine functionalities on anion binding in polyamide-containing macrocycles. Organic letters, 2009, 11, 3654-3657 |
1504082 | CIF | C31 H56 N8 O14 P2 | P 1 21/c 1 | 21.554; 20.961; 17.568 90; 97.789; 90 | 7864 | Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin The influence of amine functionalities on anion binding in polyamide-containing macrocycles. Organic letters, 2009, 11, 3654-3657 |
1504083 | CIF | C36 H52 N8 O8 | P b c a | 14.488; 18.236; 28.915 90; 90; 90 | 7639 | Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin The influence of amine functionalities on anion binding in polyamide-containing macrocycles. Organic letters, 2009, 11, 3654-3657 |
1504084 | CIF | C17 H24 N2 O4 | C 1 2 1 | 23.342; 5.7712; 17.317 90; 130.887; 90 | 1763.6 | Duguet, Nicolas; Slawin, Alexandra M. Z.; Smith, Andrew D. An asymmetric hetero-claisen approach to 3-alkyl-3-aryloxindoles. Organic letters, 2009, 11, 3858-3861 |
1504085 | CIF | C15 H13 N O3 | P 1 21/c 1 | 11.11; 5.629; 20.2 90; 96.287; 90 | 1255.7 | Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H. Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans. Organic letters, 2009, 11, 4044-4047 |
1504086 | CIF | C21 H19 N O4 S | P -1 | 8.351; 9.897; 12.327 110.85; 90.686; 101.286 | 930 | Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H. Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans. Organic letters, 2009, 11, 4044-4047 |
1504087 | CIF | C13 H15 N O2 | P 1 21/c 1 | 5.735; 15.439; 13.086 90; 110.233; 90 | 1087.2 | Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H. Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans. Organic letters, 2009, 11, 4044-4047 |
1504088 | CIF | C18 H18 Cl3 N O3 | P n a 21 | 10.096; 14.429; 13.147 90; 90; 90 | 1915.2 | Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H. Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans. Organic letters, 2009, 11, 4044-4047 |
1504089 | CIF | C18 H19 N O3 | P 1 21/n 1 | 10.6641; 7.8382; 18.3358 90; 95.948; 90 | 1524.39 | Valiulin, Roman A.; Kutateladze, Andrei G. Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems. Organic letters, 2009, 11, 3886-3889 |
1504090 | CIF | C24 H20 O2 | F d d 2 | 19.0037; 35.6919; 10.5937 90; 90; 90 | 7185.5 | Valiulin, Roman A.; Kutateladze, Andrei G. Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems. Organic letters, 2009, 11, 3886-3889 |
1504091 | CIF | C21 H20 O | P n a 21 | 21.2315; 6.5111; 10.7839 90; 90; 90 | 1490.77 | Valiulin, Roman A.; Kutateladze, Andrei G. Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems. Organic letters, 2009, 11, 3886-3889 |
1504092 | CIF | C23 H20 O2 | P 1 21/n 1 | 16.7615; 10.1571; 20.7291 90; 108.722; 90 | 3342.36 | Valiulin, Roman A.; Kutateladze, Andrei G. Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems. Organic letters, 2009, 11, 3886-3889 |
1504093 | CIF | C60 H86 O8 | P -1 | 12.5; 12.906; 18.607 78.959; 78.684; 70.333 | 2746 | Kuno, Lev; Biali, Silvio E. Restricted rotation of tert-butyl groups in sterically crowded methylene-functionalized calix[4]arenes. Organic letters, 2009, 11, 3662-3665 |
1504094 | CIF | C28 H20 O | P -1 | 9.6634; 13.954; 15.464 76.183; 88.614; 80.276 | 1995.5 | Meyer, S. Todd; Hergenrother, Paul J. Small molecule ligands for bulged RNA secondary structures. Organic letters, 2009, 11, 4052-4055 |
1504095 | CIF | C28 H20 O | P 1 21/c 1 | 17.1785; 6.5035; 17.2798 90; 101.927; 90 | 1888.8 | Meyer, S. Todd; Hergenrother, Paul J. Small molecule ligands for bulged RNA secondary structures. Organic letters, 2009, 11, 4052-4055 |
1504096 | CIF | C23 H34 O4 | C 1 2 1 | 26.323; 6.1374; 13.3377 90; 96.461; 90 | 2141.1 | Chin, Yen-Jin; Wang, Shun-Yi; Loh, Teck-Peng Synthesis of iriomoteolide-1a C13-C23 fragment via asymmetric conjugate addition and Julia-Kocienski coupling reaction. Organic letters, 2009, 11, 3674-3676 |
1504097 | CIF | C20 H26 O3 | P -1 | 8.454; 10.416; 11.534 111.416; 94.438; 104.322 | 900.2 | Beauseigneur, Alice; Ericsson, Cecilia; Renaud, Philippe; Schenk, Kurt B-Alkylcatecholborane-mediated tandem radical conjugated addition-aldol cyclization. Organic letters, 2009, 11, 3778-3781 |
1504098 | CIF | C21 H28 O3 | P -1 | 8.5042; 10.5571; 11.489 110.098; 95.633; 104.645 | 917.6 | Beauseigneur, Alice; Ericsson, Cecilia; Renaud, Philippe; Schenk, Kurt B-Alkylcatecholborane-mediated tandem radical conjugated addition-aldol cyclization. Organic letters, 2009, 11, 3778-3781 |
1504099 | CIF | C14 H14 Cl N O | P 1 21/n 1 | 9.601; 10.575; 12.022 90; 92.744; 90 | 1219.2 | Lu, Shen-Ci; Duan, Xiao-Yong; Shi, Zong-Jun; Li, Bing; Ren, Yu-Wei; Zhang, Wei; Zhang, Yong-Hui; Tu, Zhi-Feng Photoinduced Intramolecular addition of 3-acyl-2-haloindoles to alkenes. Organic letters, 2009, 11, 3902-3905 |
1504100 | CIF | C14 H14 Cl N O | P 1 21/c 1 | 9.237; 15.927; 7.966 90; 93.364; 90 | 1169.92 | Lu, Shen-Ci; Duan, Xiao-Yong; Shi, Zong-Jun; Li, Bing; Ren, Yu-Wei; Zhang, Wei; Zhang, Yong-Hui; Tu, Zhi-Feng Photoinduced Intramolecular addition of 3-acyl-2-haloindoles to alkenes. Organic letters, 2009, 11, 3902-3905 |
1504101 | CIF | C12 H11 N3 O2 | P 1 21/n 1 | 7.5084; 8.3001; 17.5331 90; 92.508; 90 | 1091.6 | Shi, Baolu; Lewis, William; Campbell, Ian B.; Moody, Christopher J. A concise route to pyridines from hydrazides by metal carbene N-H insertion, 1,2,4-triazine formation, and Diels-Alder reaction. Organic letters, 2009, 11, 3686-3688 |
1504102 | CIF | C26 H20 N2 | P 21 21 21 | 10.0514; 10.6807; 17.5467 90; 90; 90 | 1883.74 | Eisch, John J.; Manchanayakage, Renuka N.; Rheingold, Arnold L. Attempted generation of the potentially aromatic 6,7-diphenyldibenzo[e,g][1,4]diazocine dianion leads with profound rearrangement to the isomeric n-(2-amino-1,2-diphenylethenyl)carbazole dianions. Organic letters, 2009, 11, 4060-4063 |
1504103 | CIF | C26 H20 N2 | P -1 | 7.3565; 13.3596; 19.9232 92.014; 98.566; 99.128 | 1908.2 | Eisch, John J.; Manchanayakage, Renuka N.; Rheingold, Arnold L. Attempted generation of the potentially aromatic 6,7-diphenyldibenzo[e,g][1,4]diazocine dianion leads with profound rearrangement to the isomeric n-(2-amino-1,2-diphenylethenyl)carbazole dianions. Organic letters, 2009, 11, 4060-4063 |
1504104 | CIF | C27 H24 N2 O3 | P b c n | 33.2133; 7.9061; 17.9377 90; 90; 90 | 4710.2 | Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties. Organic letters, 2009, 11, 4064-4067 |
1504105 | CIF | C25 H26 N2 O3 | P -1 | 9.0795; 11.1502; 11.7893 65.448; 88.094; 78.917 | 1063.91 | Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties. Organic letters, 2009, 11, 4064-4067 |
1504106 | CIF | C27 H26 N2 O3 | P 1 21/n 1 | 10.824; 14.282; 16.681 90; 101.355; 90 | 2528.2 | Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties. Organic letters, 2009, 11, 4064-4067 |
1504107 | CIF | C25 H28 N2 O3 | P b c a | 13.0902; 16.4023; 19.4869 90; 90; 90 | 4184 | Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties. Organic letters, 2009, 11, 4064-4067 |
1504108 | CIF | C30 H48 N2 O13 | P 21 21 21 | 9.3504; 18.666; 20.153 90; 90; 90 | 3517.4 | Gao, Zheng-Xi; Wang, Meng; Wang, Shaozhong; Yao, Zhu-Jun Efficient synthesis of 4-amido-N(5)-acetyl-4-deoxyneuraminic acid and its application to the C-4 modification of sialic acids. Organic letters, 2009, 11, 3678-3681 |
1504109 | CIF | C18 H2 Br N4 O2 | P 1 21/c 1 | 7.816; 19.39; 12.728 90; 91.5; 90 | 1928.3 | Semakin, Artem N.; Sukhorukov, Alexey Yu; Lesiv, Alexey V.; Ioffe, Sema L.; Lyssenko, Konstantin A.; Nelyubina, Yulia V.; Tartakovsky, Vladimir A. Unusual intramolecular cyclization of tris(beta-oximinoalkyl)amines. the first synthesis of 1,4,6,10-tetraazaadamantanes. Organic letters, 2009, 11, 4072-4075 |
1504110 | CIF | C22 H50 N8 O16 | P 1 21 1 | 8.0368; 16.0616; 11.7596 90; 100.562; 90 | 1492.26 | Semakin, Artem N.; Sukhorukov, Alexey Yu; Lesiv, Alexey V.; Ioffe, Sema L.; Lyssenko, Konstantin A.; Nelyubina, Yulia V.; Tartakovsky, Vladimir A. Unusual intramolecular cyclization of tris(beta-oximinoalkyl)amines. the first synthesis of 1,4,6,10-tetraazaadamantanes. Organic letters, 2009, 11, 4072-4075 |
1504111 | CIF | C22 H20 Si | P -1 | 9.318; 9.838; 10.808 77.76; 68.27; 70.39 | 862.6 | Ilies, Laurean; Tsuji, Hayato; Nakamura, Eiichi Synthesis of benzo[b]siloles via KH-promoted cyclization of (2-alkynylphenyl)silanes. Organic letters, 2009, 11, 3966-3968 |
1504112 | CIF | C73 H105.74 F24 N40 Na3.33 O56.53 | C 1 2/c 1 | 51.867; 16.796; 36.2025 90; 124.185; 90 | 26089.2 | Huang, Wei-Hao; Zavalij, Peter Y.; Isaacs, Lyle Metal-ion-induced folding and dimerization of a glycoluril decamer in water. Organic letters, 2009, 11, 3918-3921 |
1504113 | CIF | C120 H174.15 F9 N80 Na7 O81.07 S2 | P -1 | 23.465; 30.5747; 31.8174 108.231; 99.079; 110.589 | 19353.8 | Huang, Wei-Hao; Zavalij, Peter Y.; Isaacs, Lyle Metal-ion-induced folding and dimerization of a glycoluril decamer in water. Organic letters, 2009, 11, 3918-3921 |
1504114 | CIF | C24 H18 Cl2 O2 | P 1 21 1 | 6.797; 27.1487; 10.6266 90; 100.197; 90 | 1929.95 | Oswald, Claire L.; Peterson, Justine A.; Lam, Hon Wai Enantioselective copper-catalyzed reductive Michael cyclizations. Organic letters, 2009, 11, 4504-4507 |
1504115 | CIF | C29 H29 Cl2 N O5 | P 1 21/c 1 | 6.1649; 8.0908; 51.2892 90; 92.662; 90 | 2555.49 | Oswald, Claire L.; Peterson, Justine A.; Lam, Hon Wai Enantioselective copper-catalyzed reductive Michael cyclizations. Organic letters, 2009, 11, 4504-4507 |
1504116 | CIF | C14 H13 N O4 S | P 1 21/n 1 | 9.2571; 13.4283; 11.0755 90; 94.92; 90 | 1371.69 | Palsuledesai, Charuta C.; Murru, Siva; Sahoo, Santosh K.; Patel, Bhisma K. Acyl-isothiocyanates as efficient thiocyanate transfer reagents. Organic letters, 2009, 11, 3382-3385 |
1504117 | CIF | C20 H16 N2 O4 S2 | C 1 2/c 1 | 32.3486; 7.7362; 18.9463 90; 124.921; 90 | 3887.7 | Palsuledesai, Charuta C.; Murru, Siva; Sahoo, Santosh K.; Patel, Bhisma K. Acyl-isothiocyanates as efficient thiocyanate transfer reagents. Organic letters, 2009, 11, 3382-3385 |
1504118 | CIF | C10 H9 N O2 S | P b c a | 9.4658; 10.2821; 19.9354 90; 90; 90 | 1940.28 | Palsuledesai, Charuta C.; Murru, Siva; Sahoo, Santosh K.; Patel, Bhisma K. Acyl-isothiocyanates as efficient thiocyanate transfer reagents. Organic letters, 2009, 11, 3382-3385 |
1504119 | CIF | C17 H15 I N2 O2 | P 1 21/n 1 | 7.8625; 10.7999; 18.3965 90; 90.968; 90 | 1561.9 | Kramer, Søren; Dooleweerdt, Karin; Lindhardt, Anders Thyboe; Rottländer, Mario; Skrydstrup, Troels Highly regioselective Au(I)-catalyzed hydroamination of ynamides and propiolic acid derivatives with anilines. Organic letters, 2009, 11, 4208-4211 |
1504120 | CIF | C27 H23 N O4 S | P 1 21 1 | 12.7746; 5.8697; 16.037 90; 102.412; 90 | 1174.4 | Lu, Hai-Hua; Zhang, Fu-Gen; Meng, Xiang-Gao; Duan, Shu-Wen; Xiao, Wen-Jing Enantioselective Michael reactions of beta, beta-disubstituted nitroalkenes: a new approach to beta(2,2)-amino acids with hetero-quaternary stereocenters. Organic letters, 2009, 11, 3946-3949 |
1504121 | CIF | C23 H23 Br N O4 S | P 1 21/c 1 | 10.96; 16.77; 12.38 90; 100.46; 90 | 2237.6 | Wei, Jun-Fa; Chen, Zhan-Guo; Lei, Wei; Zhang, Li-Hui; Wang, Ming-Zheng; Shi, Xian-Ying; Li, Run-Tao Silicon powder: the first nonmetal elemental catalyst for aminobromination of olefins with TsNH(2) and NBS. Organic letters, 2009, 11, 4216-4219 |
1504122 | CIF | C23 H21 Br N O4 S | P -1 | 10.503; 11.062; 12.012 91.99; 112.83; 116.73 | 1111.1 | Wei, Jun-Fa; Chen, Zhan-Guo; Lei, Wei; Zhang, Li-Hui; Wang, Ming-Zheng; Shi, Xian-Ying; Li, Run-Tao Silicon powder: the first nonmetal elemental catalyst for aminobromination of olefins with TsNH(2) and NBS. Organic letters, 2009, 11, 4216-4219 |
1504123 | CIF | C21 H12 N2 O | P n a 21 | 15.884; 4.626; 19.4181 90; 90; 90 | 1426.83 | Haag, Benjamin; Peng, Zhihua; Knochel, Paul Preparation of polyfunctional indazoles and heteroarylazo compounds using highly functionalized zinc reagents. Organic letters, 2009, 11, 4270-4273 |
1504124 | CIF | C18 H20 O6 | P 1 21/c 1 | 9.117; 8.628; 19.717 90; 95.16; 90 | 1544.7 | Geng, Chang-An; Jiang, Zhi-Yong; Ma, Yun-Bao; Luo, Jie; Zhang, Xue-Mei; Wang, Hong-Ling; Shen, Yong; Zuo, Ai-Xue; Zhou, Jun; Chen, Ji-Jun Swerilactones A and B, anti-HBV new lactones from a tradtional Chinese herb: Swertia mileensis as a treatment for viral hepatitis. Organic letters, 2009, 11, 4120-4123 |
1504125 | CIF | C18 H21 O6 | P 1 c 1 | 7.4578; 15.834; 7.0431 90; 111.745; 90 | 772.5 | Geng, Chang-An; Jiang, Zhi-Yong; Ma, Yun-Bao; Luo, Jie; Zhang, Xue-Mei; Wang, Hong-Ling; Shen, Yong; Zuo, Ai-Xue; Zhou, Jun; Chen, Ji-Jun Swerilactones A and B, anti-HBV new lactones from a tradtional Chinese herb: Swertia mileensis as a treatment for viral hepatitis. Organic letters, 2009, 11, 4120-4123 |
1504126 | CIF | C24 H12 | C 1 2/c 1 | 19.932; 11.06; 15.993 90; 125.953; 90 | 2854 | Umeda, Rui; Hibi, Daijiro; Miki, Koji; Tobe, Yoshito Tetradehydrodinaphtho[10]annulene: a hitherto unknown dehydroannulene and a viable precursor to stable zethrene derivatives. Organic letters, 2009, 11, 4104-4106 |
1504127 | CIF | C15 H15 Cl O2 | P 21 21 21 | 5.2032; 12.4052; 20.7454 90; 90; 90 | 1339.05 | Marqués-López, Eugenia; Herrera, Raquel P.; Marks, Timo; Jacobs, Wiebke C.; Könning, Daniel; de Figueiredo, Renata M.; Christmann, Mathias Crossed intramolecular Rauhut-Currier-type reactions via dienamine activation. Organic letters, 2009, 11, 4116-4119 |
1504128 | CIF | C42 H52 N4 O3 | P 1 21 1 | 12.7151; 8.5294; 17.2463 90; 108.811; 90 | 1770.5 | Gan, Chew-Yan; Robinson, Ward T.; Etoh, Tadahiro; Hayashi, Masahiko; Komiyama, Kanki; Kam, Toh-Seok Leucophyllidine, a cytotoxic bisindole alkaloid constituted from the union of an eburnan and a new vinylquinoline alkaloid. Organic letters, 2009, 11, 3962-3965 |
1504129 | CIF | C20 H20 O7 | P -1 | 6.9331; 8.3871; 16.424 102.313; 91.417; 97.461 | 923.81 | Zheng, Suqing; Lu, Xiyan Phosphine-catalyzed [4 + 3] annulation for the synthesis of highly functionalized bicyclo[3.2.2]nonadienes. Organic letters, 2009, 11, 3978-3981 |
1504130 | CIF | C98 H104 Cl8 N4 O2 | P 1 21/c 1 | 14.7357; 17.0703; 17.6198 90; 105.354; 90 | 4273.94 | Stepień, Marcin; Szyszko, Bartosz; Latos-Grazyński, Lechosław Steric control in the synthesis of p-benziporphyrins. Formation of a doubly N-confused benzihexaphyrin macrocycle. Organic letters, 2009, 11, 3930-3933 |
1504131 | CIF | C12 H6 O6 | A b a 2 | 10.4174; 37.939; 10.277 90; 90; 90 | 4061.7 | Li, Yan; Lampkins, Andrew J.; Baker, Matthew B.; Sumpter, Bobby G.; Huang, Jingsong; Abboud, Khalil A.; Castellano, Ronald K. Benzotrifuranone: synthesis, structure, and access to polycyclic heteroaromatics. Organic letters, 2009, 11, 4314-4317 |
1504132 | CIF | C18 B2 F12 O4 | P 1 21/n 1 | 5.998; 14.15; 9.877 90; 92.99; 90 | 837 | Ono, Katsuhiko; Hashizume, Junko; Yamaguchi, Hiroyuki; Tomura, Masaaki; Nishida, Jun-ichi; Yamashita, Yoshiro Synthesis, crystal structure, and electron-accepting property of the BF2 complex of a dihydroxydione with a perfluorotetracene skeleton. Organic letters, 2009, 11, 4326-4329 |
1504133 | CIF | C12 H16 N2 O3 S | P 1 21/n 1 | 6.2673; 25.0168; 8.7697 90; 105.982; 90 | 1321.84 | Pelletier, Sophie M.-C.; Ray, Peter C.; Dixon, Darren J. Nitro-Mannich/lactamization cascades for the direct stereoselective synthesis of pyrrolidin-2-ones. Organic letters, 2009, 11, 4512-4515 |
1504134 | CIF | C6 H7 Cl O3 | P 21 21 21 | 6.2776; 8.4084; 12.6034 90; 90; 90 | 665.27 | Pinkerton, David M.; Banwell, Martin G.; Willis, Anthony C. Chemoenzymatic access to versatile epoxyquinol synthons. Organic letters, 2009, 11, 4290-4293 |
1504135 | CIF | C6 H7 Br O3 | P 21 21 21 | 6.4569; 8.5563; 12.5272 90; 90; 90 | 692.09 | Pinkerton, David M.; Banwell, Martin G.; Willis, Anthony C. Chemoenzymatic access to versatile epoxyquinol synthons. Organic letters, 2009, 11, 4290-4293 |
1504136 | CIF | C6 H7 I O3 | P 21 21 21 | 6.8869; 8.8262; 12.2911 90; 90; 90 | 747.12 | Pinkerton, David M.; Banwell, Martin G.; Willis, Anthony C. Chemoenzymatic access to versatile epoxyquinol synthons. Organic letters, 2009, 11, 4290-4293 |
1504137 | CIF | C25 H19 N O4 | P 21 21 21 | 6.2109; 15.5608; 21.4507 90; 90; 90 | 2073.1 | Nibbs, Antoinette E.; Baize, Amanda-Lauren; Herter, Rachel M.; Scheidt, Karl A. Catalytic asymmetric alkylation of substituted isoflavanones. Organic letters, 2009, 11, 4010-4013 |
1504138 | CIF | C27 H27 Br N2 O6 S Si | P 1 21/n 1 | 15.3551; 21.005; 17.9066 90; 92.464; 90 | 5770.1 | Brawn, Ryan A.; Panek, James S. Synthesis of enantioenriched homopropargylic sulfonamides by a three component reaction of aldehydes, sulfonamides, and chiral allenylsilanes. Organic letters, 2009, 11, 4362-4365 |
1504139 | CIF | C20 H14 Br2 | P 1 21/c 1 | 9.4002; 12.978; 6.5114 90; 98.955; 90 | 784.7 | Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals. Organic letters, 2009, 11, 4026-4028 |
1504140 | CIF | C20 H14 I2 | P 1 21/c 1 | 8.8964; 4.3883; 20.521 90; 91.043; 90 | 801 | Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals. Organic letters, 2009, 11, 4026-4028 |
1504141 | CIF | C20 H14 Cl2 | P 1 21/c 1 | 9.0002; 12.78; 6.5335 90; 98.782; 90 | 742.7 | Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals. Organic letters, 2009, 11, 4026-4028 |
1504142 | CIF | C20 H14 F2 | P 1 21/c 1 | 8.272; 12.739; 6.63 90; 100.662; 90 | 686.6 | Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals. Organic letters, 2009, 11, 4026-4028 |
1504143 | CIF | C20 H14 Br2 | P 1 21/n 1 | 4.8281; 20.915; 7.4401 90; 90.051; 90 | 751.3 | Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals. Organic letters, 2009, 11, 4026-4028 |
1504144 | CIF | C20 H14 | P b c a | 7.9296; 11.5575; 14.399 90; 90; 90 | 1319.6 | Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals. Organic letters, 2009, 11, 4026-4028 |
1504145 | CIF | C40 H40 | P -1 | 10.432; 11.282; 13.32 102.375; 92.892; 106.548 | 1457.4 | Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals. Organic letters, 2009, 11, 4026-4028 |
1504146 | CIF | C20 H14 Br2 | P 1 21/n 1 | 28.496; 4.0216; 29.455 90; 110.436; 90 | 3163.1 | Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals. Organic letters, 2009, 11, 4026-4028 |
1504147 | CIF | C18 H19 N O5 | C 1 c 1 | 14.725; 16.2; 6.768 90; 91.991; 90 | 1613 | Barabé, Francis; Bétournay, Geneviève; Bellavance, Gabriel; Barriault, Louis Gold-catalyzed synthesis of carbon-bridged medium-sized rings. Organic letters, 2009, 11, 4236-4238 |
1504148 | CIF | C22 H18 Cl2 O | P 1 21 1 | 10.5484; 8.7351; 10.6236 90; 114.794; 90 | 888.64 | Ji, Yining; Riera, Antoni; Verdaguer, Xavier Asymmetric intermolecular Pauson-Khand reaction of symmetrically substituted alkynes. Organic letters, 2009, 11, 4346-4349 |
1504149 | CIF | C14 H21 N5 O4 Se | P -1 | 6.2068; 10.0735; 14.6424 105.53; 94.385; 97.243 | 869.2 | Goswami, Shyamaprosad; Hazra, Anita; Chakrabarty, Rinku; Fun, Hoong-Kun Recognition of carboxylate anions and carboxylic acids by selenium-based new chromogenic fluorescent sensor: a remarkable fluorescence enhancement of hindered carboxylates. Organic letters, 2009, 11, 4350-4353 |
1504150 | CIF | C16 H26 N2 O4 | R -3 :H | 28.99; 28.99; 10.1877 90; 90; 120 | 7414.9 | Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN 3-4'-Bipiperidines via sequential [4 + 4]-[3,3]-retro-Mannich reactions. Organic letters, 2009, 11, 4540-4543 |
1504151 | CIF | C21 H31 N2 O4 | P -1 | 8.834; 10.2781; 13.2981 90.009; 106.126; 98.122 | 1147.3 | Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN 3-4'-Bipiperidines via sequential [4 + 4]-[3,3]-retro-Mannich reactions. Organic letters, 2009, 11, 4540-4543 |
1504152 | CIF | C21 H38 N2 O7 | P -1 | 10.3811; 11.0624; 11.7553 109.649; 93.374; 115.456 | 1114.6 | Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN 3-4'-Bipiperidines via sequential [4 + 4]-[3,3]-retro-Mannich reactions. Organic letters, 2009, 11, 4540-4543 |
1504153 | CIF | C34 H25 Br N4 | P 1 21/c 1 | 9.5831; 13.0254; 23.2091 90; 96.634; 90 | 2877.6 | Yeagley, Andrew A.; Lowder, Melissa A.; Chruma, Jason J. Tandem C-C bond-forming processes: interception of the pd-catalyzed decarboxylative allylation of allyl diphenylglycinate imines with activated olefins. Organic letters, 2009, 11, 4022-4025 |
1504154 | CIF | C141 H88 F8 | P -1 | 14.2342; 16.3982; 23.0578 106.176; 91.373; 106.571 | 4922.9 | Thirion, Damien; Poriel, Cyril; Barrière, Frédéric; Métivier, Rémi; Jeannin, Olivier; Rault-Berthelot, Joëlle Tuning the optical properties of aryl-substituted dispirofluorene-indenofluorene isomers through intramolecular excimer formation. Organic letters, 2009, 11, 4794-4797 |
1504155 | CIF | C13 H8 N2 O2 S2 | P 1 21/n 1 | 7.4427; 9.3482; 18.2369 90; 95.639; 90 | 1262.71 | Murru, Siva; Ghosh, Harisadhan; Sahoo, Santosh K.; Patel, Bhisma K. Intra- and intermolecular C-S bond formation using a single catalytic system: first direct access to arylthiobenzothiazoles. Organic letters, 2009, 11, 4254-4257 |
1504156 | CIF | C28 H26 N2 O7 S | P 1 21/c 1 | 11.33; 10.825; 21.832 90; 96.054; 90 | 2662.7 | Schuler, Marie; Duvvuru, Deepti; Retailleau, Pascal; Betzer, Jean-François; Marinetti, Angela New access to trisubstituted 3-pyrrolines under phosphine catalysis. Organic letters, 2009, 11, 4406-4409 |
1504157 | CIF | C33 H43 Br O5 | P 1 21/n 1 | 18.028; 8.953; 19.479 90; 98.94; 90 | 3105.8 | Couladouros, Elias A.; Dakanali, Marianna; Demadis, Konstantinos D.; Vidali, Veroniki P. A short biomimetic approach to the fully functionalized bicyclic framework of type A acylphloroglucinols. Organic letters, 2009, 11, 4430-4433 |
1504158 | CIF | C34 H56 N12 O17 | P 1 21/m 1 | 10.4708; 19.8848; 10.7309 90; 116.395; 90 | 2001.36 | Stancl, Marek; Hodan, Martin; Sindelar, Vladimir Glycoluril trimers: selective synthesis and supramolecular properties. Organic letters, 2009, 11, 4184-4187 |
1504159 | CIF | C46 H59 I2 N14 O11.5 | P 1 21/c 1 | 15.4095; 13.0685; 25.1488 90; 94.613; 90 | 5048.04 | Stancl, Marek; Hodan, Martin; Sindelar, Vladimir Glycoluril trimers: selective synthesis and supramolecular properties. Organic letters, 2009, 11, 4184-4187 |
1504160 | CIF | C46 H60 I2 N14 O13 | P 1 21/n 1 | 14.5007; 13.3573; 27.3613 90; 93.266; 90 | 5291 | Stancl, Marek; Hodan, Martin; Sindelar, Vladimir Glycoluril trimers: selective synthesis and supramolecular properties. Organic letters, 2009, 11, 4184-4187 |
1504161 | CIF | C41 H58 I N13 O14 | P 1 21/n 1 | 13.0994; 14.8054; 24.1661 90; 92.029; 90 | 4683.88 | Stancl, Marek; Hodan, Martin; Sindelar, Vladimir Glycoluril trimers: selective synthesis and supramolecular properties. Organic letters, 2009, 11, 4184-4187 |
1504162 | CIF | C24 H38 N12 O10 | P 1 21/c 1 | 9.4511; 13.8492; 21.2892 90; 99.131; 90 | 2751.24 | Stancl, Marek; Hodan, Martin; Sindelar, Vladimir Glycoluril trimers: selective synthesis and supramolecular properties. Organic letters, 2009, 11, 4184-4187 |
1504163 | CIF | C18 H15 Br O2 | P 21 21 21 | 5.7231; 12.9531; 20.0245 90; 90; 90 | 1484.45 | Gregg, Timothy M.; Farrugia, Mark K.; Frost, John R. Rhodium-mediated enantioselective cyclopropanation of allenes. Organic letters, 2009, 11, 4434-4436 |
1504164 | CIF | C45 H40 N4 O5.5 | P 1 21/c 1 | 13.2356; 12.1782; 26.593 90; 102.202; 90 | 4189.6 | Zhou, Ying; Wang, Fang; Kim, Youngmee; Kim, Sung-Jin; Yoon, Juyoung Cu2±selective ratiometric and "off-on" sensor based on the rhodamine derivative bearing pyrene group. Organic letters, 2009, 11, 4442-4445 |
1504165 | CIF | C24 N2 O2 | P 1 21/n 1 | 9.668; 9.511; 19.728 90; 90.66; 90 | 1813.9 | Zhou, Ying; Wang, Fang; Kim, Youngmee; Kim, Sung-Jin; Yoon, Juyoung Cu2±selective ratiometric and "off-on" sensor based on the rhodamine derivative bearing pyrene group. Organic letters, 2009, 11, 4442-4445 |
1504166 | CIF | C392 H360 F48 N8 O48 P8 | P 1 21/n 1 | 16; 24.7; 24.3 90; 103.4; 90 | 9342 | Cao, Jing; Lu, Hai-Yan; You, Xiao-Jun; Zheng, Qi-Yu; Chen, Chuan-Feng Complexation of a pentiptycene-based tweezer-like receptor with paraquat derivatives: ion-controlled binding and release of the guests. Organic letters, 2009, 11, 4446-4449 |
1504167 | CIF | C20 H14 N4 S | P 1 21/c 1 | 8.9001; 11.3943; 14.9742 90; 91.902; 90 | 1517.7 | Balaji, Ganapathy; Shim, Wong Low; Parameswaran, Manoj; Valiyaveettil, Suresh Thiadiazole fused indolo[2,3-a]carbazole based oligomers and polymer. Organic letters, 2009, 11, 4450-4453 |
1504168 | CIF | C39 H40 O6 S4 | P -1 | 11.784; 15.222; 20.955 100.82; 102.15; 90.23 | 3605.6 | Kundrat, Ondrej; Dvorakova, Hana; Cisarova, Ivana; Pojarova, Michaela; Lhotak, Pavel Unusual intramolecular bridging reaction in thiacalix[4]arene series. Organic letters, 2009, 11, 4188-4191 |
1504169 | CIF | C25 H27 N3 O3 | P 1 21/c 1 | 9.7384; 12.008; 19.3474 90; 94.943; 90 | 2254 | Jiang, Gaoxi; Chen, Jian; Huang, Jie-Sheng; Che, Chi-Ming Highly efficient oxidation of amines to imines by singlet oxygen and its application in Ugi-type reactions. Organic letters, 2009, 11, 4568-4571 |
1504170 | CIF | C16 H22 O S | P 1 21/n 1 | 13.777; 6.552; 16.81 90; 108.452; 90 | 1439.4 | Liu, Taoping; Zhao, Xiaoming; Lu, Long; Cohen, Theodore Readily prepared 3-chloro-1-(phenylthio)propene, a versatile three-carbon annulating agent. Organic letters, 2009, 11, 4576-4579 |
1504171 | CIF | C18 H24 O S | P b c a | 9.2519; 16.7091; 20.816 90; 90; 90 | 3218 | Liu, Taoping; Zhao, Xiaoming; Lu, Long; Cohen, Theodore Readily prepared 3-chloro-1-(phenylthio)propene, a versatile three-carbon annulating agent. Organic letters, 2009, 11, 4576-4579 |
1504172 | CIF | C13 H20 N2 Si | P n a 21 | 10.6; 14.995; 8.7526 90; 90; 90 | 1391.2 | Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes. Organic letters, 2009, 11, 4458-4461 |
1504173 | CIF | C27 H30 N4 O2 Si | P -1 | 12.696; 14.502; 15.33 74.95; 71.74; 79.67 | 2573.6 | Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes. Organic letters, 2009, 11, 4458-4461 |
1504174 | CIF | C31 H29 Br3 N6 O4 | P -1 | 10.299; 12.584; 12.776 82.36; 88.14; 72.95 | 1568.9 | Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes. Organic letters, 2009, 11, 4458-4461 |
1504175 | CIF | C84 H27 Cl2 N O Si | P 1 21/n 1 | 19.1274; 13.9545; 19.5256 90; 108.304; 90 | 4947.96 | Matsuo, Keiko; Matsuo, Yutaka; Iwashita, Akihiko; Nakamura, Eiichi Synthesis of imino[60]fullerenes using nitriles and trimethylsilylmethyl triflate. Organic letters, 2009, 11, 4192-4194 |
1504176 | CIF | C22 H26 N2 O2 | P 1 21/c 1 | 8.816; 13.762; 31.213 90; 94.584; 90 | 3774.83 | Grant, Christopher D.; Krische, Michael J. Protecting-group-free synthesis of 3-tert-prenylated oxindoles: contiguous all-carbon quaternary centers via tertiary neopentyl substitution. Organic letters, 2009, 11, 4485-4487 |
1504177 | CIF | C22 H19 N O5 | P 21 21 21 | 5.7776; 16.337; 20.021 90; 90; 90 | 1889.8 | Li, Hongyan; Hsung, Richard P. Highly substituted 2-amido-furans from Rh(II)-catalyzed cyclopropenations of ynamides. Organic letters, 2009, 11, 4462-4465 |
1504178 | CIF | C79 H95 F12 N7 O16 P2 | P -1 | 14.3156; 15.2385; 21.0682 86.801; 82.424; 66.377 | 4174.1 | Yen, Ming-Liang; Chen, Nai-Chia; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien A molecular cage that selectively complexes three different guests in solution. Organic letters, 2009, 11, 4604-4607 |
1504179 | CIF | C28 H27 Cl Cu0.5 N9 O2 | P -1 | 9.6706; 11.7736; 12.4516 80.677; 81.72; 81.309 | 1372.5 | Ozçubukçu, Salih; Ozkal, Erhan; Jimeno, Ciril; Pericàs, Miquel A A highly active catalyst for Huisgen 1,3-dipolar cycloadditions based on the tris(triazolyl)methanol-Cu(I) structure. Organic letters, 2009, 11, 4680-4683 |
1504180 | CIF | C20 H20 O8 | P 1 21 1 | 6.547; 10.892; 12.418 90; 103.542; 90 | 860.9 | Geng, Chang-An; Zhang, Xue-Mei; Shen, Yong; Zuo, Ai-Xue; Liu, Ji-Feng; Ma, Yun-Bao; Luo, Jie; Zhou, Jun; Jiang, Zhi-yong; Chen, Ji-Jun Swerilactones C and D, anti-HBV new lactones from a traditional Chinese herb: Swertia mileensis. Organic letters, 2009, 11, 4838-4841 |
1504181 | CIF | C20 H22 O9 | P -1 | 8.6844; 14.094; 17 73.293; 87.688; 72.958 | 1903.2 | Geng, Chang-An; Zhang, Xue-Mei; Shen, Yong; Zuo, Ai-Xue; Liu, Ji-Feng; Ma, Yun-Bao; Luo, Jie; Zhou, Jun; Jiang, Zhi-yong; Chen, Ji-Jun Swerilactones C and D, anti-HBV new lactones from a traditional Chinese herb: Swertia mileensis. Organic letters, 2009, 11, 4838-4841 |
1504182 | CIF | C24 H36 Cl N2 O7 | P 21 21 21 | 9.268; 13.934; 19.073 90; 90; 90 | 2463.1 | Feng, Tao; Cai, Xiang-Hai; Li, Yan; Wang, Yuan-Yuan; Liu, Ya-Ping; Xie, Ming-Jin; Luo, Xiao-Dong Melohenines A and B, two unprecedented alkaloids from Melodinus henryi Organic Letters, 2009, 11, 4834-4837 |
1504183 | CIF | C19 H24 N2 O3 | P 21 21 21 | 7.9717; 12.2181; 17.265 90; 90; 90 | 1681.6 | Feng, Tao; Cai, Xiang-Hai; Li, Yan; Wang, Yuan-Yuan; Liu, Ya-Ping; Xie, Ming-Jin; Luo, Xiao-Dong Melohenines A and B, two unprecedented alkaloids from Melodinus henryi Organic Letters, 2009, 11, 4834-4837 |
1504184 | CIF | C15 H11 N3 O2 | P 1 21/c 1 | 19.1116; 4.165; 16.2443 90; 111.391; 90 | 1203.97 | Board, Johnathan; Wang, Jian-Xin; Crew, Andrew P.; Jin, Meizhong; Foreman, Kenneth; Mulvihill, Mark J.; Snieckus, Victor Synthesis of substituted imidazo[1,5-a]pyrazines via mono-, di-, and directed remote metalation strategies. Organic letters, 2009, 11, 5118-5121 |
1504185 | CIF | C16 H18 O4 | C 1 2 1 | 18.1933; 7.711; 12.4502 90; 129.39; 90 | 1349.87 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
1504186 | CIF | C16 H18 O5 | P 21 21 21 | 7.8053; 9.4883; 18.9039 90; 90; 90 | 1400 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
1504187 | CIF | C17 H20 O5 | C 1 2 1 | 18.1525; 7.6684; 12.0226 90; 101.178; 90 | 1641.81 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
1504188 | CIF | C16 H18 O5 | P 21 21 21 | 9.597; 9.9935; 14.1873 90; 90; 90 | 1360.67 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
1504189 | CIF | C19 H24 O4 | P 21 21 21 | 7.7249; 9.6338; 22.5067 90; 90; 90 | 1674.95 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
1504190 | CIF | C19 H22 O4 | P 21 21 21 | 7.7635; 9.7864; 21.0195 90; 90; 90 | 1596.99 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
1504191 | CIF | C17 H20 O6 | P 21 21 21 | 6.1894; 8.9465; 28.8255 90; 90; 90 | 1596.17 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
1504192 | CIF | C16 H18 O6 | P 21 21 21 | 8.2864; 10.0771; 17.1744 90; 90; 90 | 1434.11 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
1504193 | CIF | C17 H20 O6 | P 21 21 21 | 11.0321; 11.6526; 11.9913 90; 90; 90 | 1541.51 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
1504194 | CIF | C15 H22 O3 | P -1 | 8.8984; 9.621; 16.7771 89.599; 85.959; 85.973 | 1429.2 | Hampel, Thomas; Brückner, Reinhard A novel cis-selective cyclohexanone annulation as the key step of a total synthesis of the sesquiterpene isoacanthodoral. Organic letters, 2009, 11, 4842-4845 |
1504195 | CIF | C18 H13 F3 O9 S | P 1 21/c 1 | 18.964; 13.633; 29.823 90; 92.316; 90 | 7704 | Cui, Yi; Jiang, Hao; Li, Zhengtao; Wu, Na; Yang, Zhen; Quan, Junmin Unexpected regioselectivity in the synthesis of pyranonaphthoquinone via the Diels-Alder reaction. Organic letters, 2009, 11, 4628-4631 |
1504196 | CIF | C9 H12 O3 S | P 1 21 1 | 7.6288; 5.445; 11.5547 90; 91.844; 90 | 479.72 | Majer, Jakub; Kwiatkowski, Piotr; Jurczak, Janusz Highly enantioselective Friedel-Crafts reaction of thiophenes with glyoxylates: formal synthesis of duloxetine. Organic letters, 2009, 11, 4636-4639 |
1504197 | CIF | C18 H27 N O6 | P 21 21 21 | 9.355; 11.918; 17.31 90; 90; 90 | 1929.9 | Gross, Ulrike; Nieger, Martin; Bräse, Stefan Stereoselective synthesis of the epicoccin core. Organic letters, 2009, 11, 4740-4742 |
1504198 | CIF | C22 H27 N O7 | P 1 21 1 | 7.715; 15.086; 9.295 90; 96.54; 90 | 1074.8 | Balthaser, Bradley R.; McDonald, Frank E. Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins. Organic letters, 2009, 11, 4850-4853 |
1504199 | CIF | C22 H27 N O7 | P 1 21 1 | 13.2879; 9.2997; 17.411 90; 100.194; 90 | 2117.57 | Balthaser, Bradley R.; McDonald, Frank E. Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins. Organic letters, 2009, 11, 4850-4853 |
1504200 | CIF | C22 H35 N O11 | P 21 21 21 | 8.1737; 10.9997; 29.222 90; 90; 90 | 2627.3 | Balthaser, Bradley R.; McDonald, Frank E. Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins. Organic letters, 2009, 11, 4850-4853 |
1504201 | CIF | C28.5 H31 Cl | C 1 2/c 1 | 25.9973; 12.3802; 13.8796 90; 93.724; 90 | 4457.74 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
1504202 | CIF | C30 H34 | P -1 | 11.075; 14.841; 15.693 118.089; 91.405; 92.655 | 2270 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
1504203 | CIF | C30 H34 O2 | P 1 21/c 1 | 10.6975; 10.0435; 10.8065 90; 101.43; 90 | 1138.03 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
1504204 | CIF | C30 H34 O2 | P 1 21/c 1 | 14.0575; 10.3006; 8.0732 90; 99.533; 90 | 1152.86 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
1504205 | CIF | C30 H34 O2.96 | R -3 :H | 21.0561; 21.0561; 14.3941 90; 90; 120 | 5526.77 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
1504206 | CIF | C32 H38 O4 | P 1 21/n 1 | 9.6612; 6.9042; 19.3657 90; 94.574; 90 | 1287.63 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
1504207 | CIF | C48 H54 | P 1 21/c 1 | 21.8162; 9.4664; 8.9027 90; 90.648; 90 | 1838.5 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
1504208 | CIF | C66 H86 | P 1 21/n 1 | 11.9837; 36.2583; 18.6597 90; 95.013; 90 | 8076.8 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
1504209 | CIF | C40 H50 Cl4 O4 | P 1 21/c 1 | 12.5705; 9.6243; 15.996 90; 106.347; 90 | 1857 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
1504210 | CIF | C23 H22 Cl N O3 | P 1 21 1 | 10.185; 8.74; 12.189 90; 112.29; 90 | 1003.9 | Han, Bo; Xiao, You-Cai; He, Zhao-Quan; Chen, Ying-Chun Asymmetric Michael addition of gamma,gamma-disubstituted alpha,beta-unsaturated aldehydes to nitroolefins via dienamine catalysis. Organic letters, 2009, 11, 4660-4663 |
1504211 | CIF | C12 H9 N O4 | P 1 21/n 1 | 6.0584; 19.717; 8.9513 90; 98.257; 90 | 1058.2 | Huo, Fang-Jun; Sun, Yuan-Qiang; Su, Jing; Chao, Jian-Bin; Zhi, Hai-Juan; Yin, Cai-Xia Colorimetric detection of thiols using a chromene molecule Organic letters, 2009, 11, 4918-4921 |
1504212 | CIF | C17 H15 B F4 O3 | P 1 21/n 1 | 12.7974; 7.6261; 17.351 90; 105.01; 90 | 1635.6 | Hu, Zhi-Long; Qian, Wen-Jian; Wang, Sheng; Wang, Shaozhong; Yao, Zhu-Jun Transformation of reactive isochromenylium intermediates to stable salts and their cascade reactions with olefins. Organic letters, 2009, 11, 4676-4679 |
1504213 | CIF | C21 H28 O10 | P 21 21 21 | 10.0245; 12.5364; 17.6378 90; 90; 90 | 2216.6 | Afarinkia, Kamyar; Abdullahi, Mohamed Haji; Scowen, Ian J. A new, general method for the synthesis of carbasugar-sugar pseudodisaccharides. Organic letters, 2009, 11, 5182-5184 |
1504214 | CIF | C25 H40 O5 Si | P 21 21 21 | 6.5381; 13.0869; 28.301 90; 90; 90 | 2421.5 | Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S. A synthesis of the carbon skeleton of maoecrystal V. Organic letters, 2009, 11, 4774-4776 |
1504215 | CIF | C27 H40 O7 Si | C 1 2 1 | 27.8634; 7.012; 18.3625 90; 129.332; 90 | 2774.98 | Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S. A synthesis of the carbon skeleton of maoecrystal V. Organic letters, 2009, 11, 4774-4776 |
1504216 | CIF | C21 H24 O6 | P 1 21/n 1 | 7.1446; 10.9191; 23.7565 90; 91.941; 90 | 1852.24 | Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S. A synthesis of the carbon skeleton of maoecrystal V. Organic letters, 2009, 11, 4774-4776 |
1504217 | CIF | C21 H27 O7 | C 1 2 1 | 30.4299; 7.0493; 19.6268 90; 111.309; 90 | 3922.31 | Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S. A synthesis of the carbon skeleton of maoecrystal V. Organic letters, 2009, 11, 4774-4776 |
1504218 | CIF | C26 H21 O3 | P 1 | 8.4452; 10.6647; 11.566 82.23; 89.149; 77.425 | 1007.26 | Yoshida, Masahiro; Higuchi, Mariko; Shishido, Kozo Stereoselective construction of substituted chromans by palladium-catalyzed cyclization of propargylic carbonates with 2-(2-hydroxyphenyl)acetates. Organic letters, 2009, 11, 4752-4755 |
1504219 | CIF | C26 H33 N O3 Si | P 1 | 7.718; 11.898; 14.296 96.932; 103.456; 108.338 | 1184.9 | Tietze, Lutz F.; Tölle, Nina; Kratzert, Daniel; Stalke, Dietmar Efficient formal total synthesis of the erythrina alkaloid (+)-erysotramidine, using a domino process. Organic letters, 2009, 11, 5230-5233 |
1504220 | CIF | C18 H21 N O4 | P 1 21/n 1 | 10.762; 12.294; 11.66 90; 106.56; 90 | 1478.7 | Tietze, Lutz F.; Tölle, Nina; Kratzert, Daniel; Stalke, Dietmar Efficient formal total synthesis of the erythrina alkaloid (+)-erysotramidine, using a domino process. Organic letters, 2009, 11, 5230-5233 |
1504221 | CIF | C29 H22 O2 | C 1 2/c 1 | 25.5017; 10.0101; 18.5411 90; 118.749; 90 | 4149.6 | Zhang, Xiaoxiang; Teo, Wan Teng; Chan, Philip Wai Hong Ytterbium(III) triflate catalyzed tandem Friedel-Crafts alkylation/hydroarylation of propargylic alcohols with phenols as an expedient route to indenols. Organic letters, 2009, 11, 4990-4993 |
1504222 | CIF | C20 H24 O2 | P 1 21/n 1 | 14.0468; 6.6546; 18.8942 90; 110.607; 90 | 1653.15 | Falck, J. R.; Bandyopadhyay, Anish; Puli, Narender; Kundu, Abhijit; Reddy, L. Manmohan; Barma, Deb K.; He, Anyu; Zhang, Hongming; Kashinath, Dhurke; Baati, Rachid Cascade synthesis of (E)-2-alkylidenecyclobutanols. Organic letters, 2009, 11, 4764-4766 |
1504223 | CIF | C20 H28 N2 O5 S | P 1 21 1 | 11.9221; 10.8903; 16.4113 90; 105.351; 90 | 2054.74 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504224 | CIF | C15 H19 N O4 S | P 21 21 21 | 22.7128; 8.0293; 8.0067 90; 90; 90 | 1460.16 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504225 | CIF | C21 H23 N O4 S | P 1 21 1 | 7.8477; 11.5372; 10.5434 90; 108.089; 90 | 907.42 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504226 | CIF | C16 H21 N O4 S | P 21 21 2 | 12.1704; 17.3626; 7.5061 90; 90; 90 | 1586.11 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504227 | CIF | C18 H26 O2 Si | P 1 21 1 | 5.9876; 7.3491; 19.9858 90; 97.689; 90 | 871.54 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504228 | CIF | C23 H29 N O4 S | P 21 21 21 | 8.0984; 13.6158; 19.1081 90; 90; 90 | 2106.98 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504229 | CIF | C23 H27 N O4 S | P 41 21 2 | 10.834; 10.834; 36.399 90; 90; 90 | 4272.35 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504230 | CIF | C21 H23 N O4 S | P 21 21 21 | 7.76; 8.8993; 27.238 90; 90; 90 | 1881.02 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504231 | CIF | C26 H37 Cl N2 O4 S | P 21 21 21 | 7.144; 11.902; 30.0352 90; 90; 90 | 2553.83 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504232 | CIF | C26 H31 Cl N2 O4 S | P 21 21 21 | 7.1052; 11.8008; 28.9702 90; 90; 90 | 2429.07 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504233 | CIF | C25 H32 N O4 S | P 1 21 1 | 10.3654; 10.9898; 10.6563 90; 104.714; 90 | 1174.09 | Webster, Robert; Lautens, Mark Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles. Organic letters, 2009, 11, 4688-4691 |
1504234 | CIF | C18 H26 O3 | P 1 21 1 | 6.7635; 13.1016; 9.4936 90; 99.898; 90 | 828.7 | Tseng, Yen-Ju; Wen, Zhi-Hong; Dai, Chang-Feng; Chiang, Michael Y.; Sheu, Jyh-Horng Nanolobatolide, a new C18 metabolite from the Formosan soft coral Sinularia nanolobata. Organic letters, 2009, 11, 5030-5032 |
1504235 | CIF | C24 H20 O2 | P n a 21 | 10.3835; 18.167; 9.6747 90; 90; 90 | 1825 | Onodera, Gen; Kato, Minoru; Kawano, Ryo; Kometani, Yuri; Takeuchi, Ryo Highly regio- and stereoselective addition of 1,3-diketones to internal alkynes catalyzed by cationic iridium complex. Organic letters, 2009, 11, 5038-5041 |
1504236 | CIF | C15 H17 N O4 | P b c a | 9.03; 11.494; 26.562 90; 90; 90 | 2757 | Kise, Naoki; Isemoto, Shinsaku; Sakurai, Toshihiko Electroreductive coupling of phthalimides with alpha,beta-unsaturated esters: unusual rearrangement of resulting silyl ketene acetals. Organic letters, 2009, 11, 4902-4905 |
1504237 | CIF | C16 H19 N O4 | P b c a | 9.4786; 10.8076; 28.163 90; 90; 90 | 2885 | Kise, Naoki; Isemoto, Shinsaku; Sakurai, Toshihiko Electroreductive coupling of phthalimides with alpha,beta-unsaturated esters: unusual rearrangement of resulting silyl ketene acetals. Organic letters, 2009, 11, 4902-4905 |
1504238 | CIF | C14 H11 N O3 | P -1 | 7.7; 8.873; 16.958 99.1; 101.15; 92.16 | 1119.6 | Kise, Naoki; Isemoto, Shinsaku; Sakurai, Toshihiko Electroreductive coupling of phthalimides with alpha,beta-unsaturated esters: unusual rearrangement of resulting silyl ketene acetals. Organic letters, 2009, 11, 4902-4905 |
1504239 | CIF | C13 H13 N O3 | P 1 21/a 1 | 7.578; 17.794; 8.169 90; 87.67; 90 | 1100.6 | Kise, Naoki; Isemoto, Shinsaku; Sakurai, Toshihiko Electroreductive coupling of phthalimides with alpha,beta-unsaturated esters: unusual rearrangement of resulting silyl ketene acetals. Organic letters, 2009, 11, 4902-4905 |
1504240 | CIF | C38.76 H26.76 Cl2.28 N2 O4 | P 1 21/n 1 | 14.1491; 15.475; 14.3939 90; 90.06; 90 | 3151.6 | Maugel, Nathan; Snider, Barry B. Efficient synthesis of the tetracyclic aminoquinone moiety of marmycin A. Organic letters, 2009, 11, 4926-4929 |
1504241 | CIF | C23 H28 O3 S | P 1 21 1 | 11.0848; 8.9222; 11.2461 90; 116.209; 90 | 997.9 | Hernández-Torres, Gloria; Urbano, Antonio; Carreño, M Carmen; Colobert, Françoise Stereocontrolled generation of the (2R) chroman core of vitamin E: total synthesis of (2R,4'RS,8'RS)-alpha-tocopherol. Organic letters, 2009, 11, 4930-4933 |
1504242 | CIF | C20 H17 Cl2 N O | P 21 21 21 | 12.5109; 15.341; 17.9478 90; 90; 90 | 3444.72 | Oinen, Mark Emil; Yu, Robert T.; Rovis, Tomislav Excess substrate is a spectator ligand in a rhodium-catalyzed asymmetric [2 + 2 + 2] cycloaddition of alkenyl isocyanates with tolanes. Organic letters, 2009, 11, 4934-4937 |
1504243 | CIF | C35 H27 Br Cl3 N O6 | P 1 21 1 | 15.8; 5.833; 18.339 90; 99.491; 90 | 1667 | Yu, Jie; He, Long; Chen, Xiao-Hua; Song, Jin; Chen, Wei-Jie; Gong, Liu-Zhu Highly enantioselective catalytic 1,3-dipolar cycloaddition involving 2,3-allenoate dipolarophiles. Organic letters, 2009, 11, 4946-4949 |
1504244 | CIF | C23 H21 N O4 S2 | P 21 21 21 | 6.0566; 11.2097; 30.664 90; 90; 90 | 2081.9 | Moreno-Clavijo, Elena; Carmona, Ana T.; Reissig, Hans-Ulrich; Moreno-Vargas, Antonio J; Alvarez, Eleuterio; Robina, Inmaculada Allenyl sulfones and allenyl sulfides in the synthesis of 3-pyrrolines. A novel nucleophilic [3 + 2] cycloaddition on allenyl sulfones giving rearranged cycloadducts. Organic letters, 2009, 11, 4778-4781 |
1504245 | CIF | C24 H23 N O5 S2 | P 21 21 21 | 5.9508; 11.729; 31.384 90; 90; 90 | 2190.5 | Moreno-Clavijo, Elena; Carmona, Ana T.; Reissig, Hans-Ulrich; Moreno-Vargas, Antonio J; Alvarez, Eleuterio; Robina, Inmaculada Allenyl sulfones and allenyl sulfides in the synthesis of 3-pyrrolines. A novel nucleophilic [3 + 2] cycloaddition on allenyl sulfones giving rearranged cycloadducts. Organic letters, 2009, 11, 4778-4781 |
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