Crystallography Open Database

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Searching journal of publication like 'Organic letters' volume of publication is 18

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1555535 CIFC19 H25 Cl N O RhP 1 21/c 113.0578; 15.8566; 18.5108
90; 91.055; 90
3832.1Wang, Qiang; Li, Xingwei
Synthesis of 1H-Indazoles from Imidates and Nitrosobenzenes via Synergistic Rhodium/Copper Catalysis.
Organic letters, 2016, 18, 2102-2105
1555536 CIFC15 H15 Br O3 SP 1 21 15.92604; 12.2676; 9.9444
90; 103.755; 90
702.21Pagire, Santosh K.; Paria, Suva; Reiser, Oliver
Synthesis of β-Hydroxysulfones from Sulfonyl Chlorides and Alkenes Utilizing Visible Light Photocatalytic Sequences.
Organic letters, 2016, 18, 2106-2109
1555537 CIFC46 H39 Au2 F6 N O5 P2 S3P 1 c 114.011; 16.7528; 20.7802
90; 105.001; 90
4711.4Tamai, Taichi; Fujiwara, Keiko; Higashimae, Shinya; Nomoto, Akihiro; Ogawa, Akiya
Gold-Catalyzed Anti-Markovnikov Selective Hydrothiolation of Unactivated Alkenes.
Organic letters, 2016, 18, 2114-2117
1555538 CIFC12 H13 N O2P 1 21/n 19.8079; 8.8394; 12.567
90; 99.596; 90
1074.3Fraboni, Americo J.; Brenner-Moyer, Stacey E
Dienamine-Catalyzed Nitrone Formation via Redox Reaction.
Organic letters, 2016, 18, 2146-2149
1555539 CIFC16 H15 Br Cl3 N O2P -17.5091; 10.1225; 12.5419
76.957; 81.066; 75.302
893.46García-García, Carolina; Ortiz-Rojano, Laura; Álvarez, Susana; Álvarez, Rosana; Ribagorda, María; Carreño, M Carmen
Friedel-Crafts Alkylation of Indoles with p-Quinols: The Role of Hydrogen Bonding of Water for the Desymmetrization of the Cyclohexadienone System.
Organic letters, 2016, 18, 2224-2227
1555540 CIFC17 H11 N OP -13.991; 10.967; 15.118
73.536; 86.417; 81.507
627.5Wang, Lianjie; Liu, Xiaocui; Wang, Mang; Liu, Jun
Copper(I)-Catalyzed Heterocyclization of α-Acyl-α-alkynyl Ketene Dithioacetals: Synthesis of 3-Cyanofurans.
Organic letters, 2016, 18, 2162-2165
1555541 CIFC20 H27 O3.5I 4119.7536; 19.7536; 9.0366
90; 90; 90
3526.1Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555542 CIFC20 H26 O3P 21 21 219.7169; 10.1381; 17.5286
90; 90; 90
1726.76Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555543 CIFC22 H32 O4C 1 2 118.2916; 8.7712; 12.993
90; 103.232; 90
2029.24Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555544 CIFC22 H20 Br N O2P 1 21 18.6651; 5.8524; 18.9495
90; 93.712; 90
958.94Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555545 CIFC24 H25 N O4P 112.7971; 12.8656; 14.0933
88.968; 86.108; 66.582
2124.21Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555546 CIFC28 H25 N O2P 21 21 215.9977; 8.669; 42.0392
90; 90; 90
2185.79Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555547 CIFC40 H40 N2 O SP -110.2707; 12.5581; 14.2615
78.265; 69.761; 81.577
1684Makarov, Anton S.; Merkushev, Anton A.; Uchuskin, Maxim G.; Trushkov, Igor V.
Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues.
Organic letters, 2016, 18, 2192-2195
1555548 CIFC26 H25 Cl2 N O4 SP -19.9795; 10.2314; 12.8722
92.489; 106.194; 96.538
1250.1Makarov, Anton S.; Merkushev, Anton A.; Uchuskin, Maxim G.; Trushkov, Igor V.
Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues.
Organic letters, 2016, 18, 2192-2195
1555549 CIFC21 H15 NP -110.3062; 11.6276; 13.2088
75.92; 88.72; 87.09
1533.28Saunthwal, Rakesh K.; Patel, Monika; Verma, Akhilesh K.
Metal- and Protection-Free [4 + 2] Cycloadditions of Alkynes with Azadienes: Assembly of Functionalized Quinolines.
Organic letters, 2016, 18, 2200-2203
1555550 CIFC12 H9 F3 N2 OP 1 21/c 19.3458; 13.3878; 9.015
90; 104.592; 90
1091.57Nguyen, Thanh Binh; Ermolenko, Ludmila; Retailleau, Pascal; Al-Mourabit, Ali
Molecular Iodine-Catalyzed Aerobic α,β-Diamination of Cyclohexanones with 2-Aminopyrimidine and 2-Aminopyridines.
Organic letters, 2016, 18, 2177-2179
1555551 CIFC16 H18 N2 O2P 1 21 18.94706; 11.2291; 14.9983
90; 102.552; 90
1470.83Halskov, Kim Søholm; Næsborg, Line; Tur, Fernando; Jørgensen, Karl Anker
Asymmetric [3 + 2] Cycloaddition of Vinylcyclopropanes and α,β-Unsaturated Aldehydes by Synergistic Palladium and Organocatalysis.
Organic letters, 2016, 18, 2220-2223
1555552 CIFC8 H9 Cl N4 OP 21 21 215.3345; 17.4841; 6.9026
90; 90; 90
1850.7Sun, Huan-Li; Chen, Fei; Xie, Ming-Sheng; Guo, Hai-Ming; Qu, Gui-Rong; He, Yan-Mei; Fan, Qing-Hua
Asymmetric Hydrogenation of α-Purine Nucleobase-Substituted Acrylates with Rhodium Diphosphine Complexes: Access to Tenofovir Analogues.
Organic letters, 2016, 18, 2260-2263
1555553 CIFC18 H22 F N O4P 21 21 219.7821; 11.5835; 14.8591
90; 90; 90
1683.7Zhu, Luyi; Chen, Qiliang; Shen, Dan; Zhang, Weihao; Shen, Cong; Zeng, Xiaofei; Zhong, Guofu
Enantioselective Construction of Spirocyclic Oxindole Derivatives with Multiple Stereocenters via an Organocatalytic Michael/Aldol/Hemiacetalization Cascade Reaction.
Organic letters, 2016, 18, 2387-2390
1555554 CIFC28 H24 O6 S2P 1 21/c 116.268; 7.4469; 22.374
90; 110.413; 90
2540.3Ni, Chunjie; Wang, MingLi; Tong, Xiaofeng
Access to Thiophene and 1H-Pyrrole via Amine-Initiated (3 + 2) Annulation and Aromatization Cascade Reaction of β'-Acetoxy Allenoate and 1,2-Bisnucleophile.
Organic letters, 2016, 18, 2240-2243

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