Crystallography Open Database
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Searching journal of publication like 'Organic letters' volume of publication is 16
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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1517230 | CIF | C18 H26 O4 | P -1 | 8.1038; 13.1776; 16.2542 71.565; 85.809; 75.309 | 1592.81 | Clark, J. Stephen; Delion, Laetitia; Farrugia, Louis J. Total synthesis of the purported structure of sclerophytin f. Organic letters, 2014, 16, 4300-4303 |
1517231 | CIF | C20 H32 O4 | P 21 21 21 | 5.624; 16.55; 19.16 90; 90; 90 | 1783.4 | Clark, J. Stephen; Delion, Laetitia; Farrugia, Louis J. Total synthesis of the purported structure of sclerophytin f. Organic letters, 2014, 16, 4300-4303 |
1517232 | CIF | C16 H23 N O2 S | P 1 21 1 | 5.526; 11.111; 13.716 90; 98.463; 90 | 833 | Su, Lin; Zhu, Ting-Shun; Xu, Ming-Hua Indium-Mediated Asymmetric Intramolecular Allenylation of N-tert-Butanesulfinyl Imines: Efficient and Practical Access to Chiral 3-Allenyl-4-aminochromanes. Organic letters, 2014, 16, 4118-4121 |
1517233 | CIF | C19 H21 N O3 S | P 1 | 7.176; 10.859; 12.059 100.648; 106.125; 95.565 | 876.2 | Su, Lin; Zhu, Ting-Shun; Xu, Ming-Hua Indium-Mediated Asymmetric Intramolecular Allenylation of N-tert-Butanesulfinyl Imines: Efficient and Practical Access to Chiral 3-Allenyl-4-aminochromanes. Organic letters, 2014, 16, 4118-4121 |
1517234 | CIF | C16 H17 N O2 S | C 1 2 1 | 19.1174; 6.6815; 13.5889 90; 110.988; 90 | 1620.59 | Su, Lin; Zhu, Ting-Shun; Xu, Ming-Hua Indium-Mediated Asymmetric Intramolecular Allenylation of N-tert-Butanesulfinyl Imines: Efficient and Practical Access to Chiral 3-Allenyl-4-aminochromanes. Organic letters, 2014, 16, 4118-4121 |
1517235 | CIF | C19 H21 N O3 S | P 1 21 1 | 11.8178; 6.1413; 12.0958 90; 95.858; 90 | 873.29 | Su, Lin; Zhu, Ting-Shun; Xu, Ming-Hua Indium-Mediated Asymmetric Intramolecular Allenylation of N-tert-Butanesulfinyl Imines: Efficient and Practical Access to Chiral 3-Allenyl-4-aminochromanes. Organic letters, 2014, 16, 4118-4121 |
1517236 | CIF | C14 H13 N O5 | P b c a | 6.9386; 15.1121; 23.6998 90; 90; 90 | 2485.09 | Logan, Angus W. J.; Sprague, Simon J.; Foster, Robert W.; Marx, Léo B; Garzya, Vincenzo; Hallside, Michal S.; Thompson, Amber L.; Burton, Jonathan W. Diastereoselective synthesis of fused lactone-pyrrolidinones; application to a formal synthesis of (-)-salinosporamide a. Organic letters, 2014, 16, 4078-4081 |
1517237 | CIF | C26 H35 N O6 | P 21 21 21 | 6.2769; 19.0465; 20.3494 90; 90; 90 | 2432.83 | Logan, Angus W. J.; Sprague, Simon J.; Foster, Robert W.; Marx, Léo B; Garzya, Vincenzo; Hallside, Michal S.; Thompson, Amber L.; Burton, Jonathan W. Diastereoselective synthesis of fused lactone-pyrrolidinones; application to a formal synthesis of (-)-salinosporamide a. Organic letters, 2014, 16, 4078-4081 |
1517247 | CIF | C21 H23 N O4 | P 1 21 1 | 9.6514; 13.5727; 28.8023 90; 99.6158; 90 | 3720 | Azuma, Takumi; Murata, Akihiro; Kobayashi, Yusuke; Inokuma, Tsubasa; Takemoto, Yoshiji A Dual Arylboronic Acid-Aminothiourea Catalytic System for the Asymmetric Intramolecular Hetero-Michael Reaction of α,β-Unsaturated Carboxylic Acids. Organic letters, 2014, 16, 4256-4259 |
1517248 | CIF | C10 H12 O4 | I 41/a :2 | 19.225; 19.225; 10.568 90; 90; 90 | 3906 | Kasare, Sanghratna; Bankar, Siddheshwar K.; Ramasastry, S. S. V. Expeditious Metal-Free Access to Functionalized Polycyclic Acetals under Mild Aqueous Conditions. Organic letters, 2014, 16, 4284-4287 |
1517249 | CIF | C15 H22 O5 | C 1 c 1 | 10.478; 15.304; 9.535 90; 104.6; 90 | 1479.6 | Kasare, Sanghratna; Bankar, Siddheshwar K.; Ramasastry, S. S. V. Expeditious Metal-Free Access to Functionalized Polycyclic Acetals under Mild Aqueous Conditions. Organic letters, 2014, 16, 4284-4287 |
1517250 | CIF | C25 H17 Cl2 N O | P 1 21/n 1 | 6.8744; 14.0493; 20.5936 90; 90.272; 90 | 1988.92 | Mothe, Srinivasa Reddy; Novianti, Maria Laurentia; Ayers, Benjamin James; Chan, Philip Wai Hong Silver-Catalyzed Tandem Hydroamination/Hydroarylation of 1-(2-Allylamino)phenyl-4-hydroxy-but-2-yn-1-ones to 1'-Allylspiro[indene-1,2'-indolin]-3'-ones. Organic letters, 2014, 16, 4110-4113 |
1517251 | CIF | C19 H19 N O2 | P 1 21/c 1 | 11.5674; 18.339; 7.6496 90; 108.4; 90 | 1539.8 | Xiao, Tiebo; Li, Linyong; Lin, Guoliang; Mao, Zong-Wan; Zhou, Lei Metal-free visible-light induced cross-dehydrogenative coupling of tertiary amines with diazo compounds. Organic letters, 2014, 16, 4232-4235 |
1517252 | CIF | C19 H18 Cl N O2 | P 1 21/n 1 | 10.4739; 14.9845; 10.5112 90; 96.966; 90 | 1637.5 | Xiao, Tiebo; Li, Linyong; Lin, Guoliang; Mao, Zong-Wan; Zhou, Lei Metal-free visible-light induced cross-dehydrogenative coupling of tertiary amines with diazo compounds. Organic letters, 2014, 16, 4232-4235 |
1517253 | CIF | C29 H33 N3 O2 | P c a 21 | 25.7585; 10.3249; 9.5675 90; 90; 90 | 2544.51 | Galvez, Jaime; Castillo, Juan-Carlos; Quiroga, Jairo; Rajzmann, Michel; Rodriguez, Jean; Coquerel, Yoann Divergent Chemo-, Regio-, and Diastereoselective Normal Electron-Demand Povarov-Type Reactions with α-Oxo-ketene Dienophiles. Organic letters, 2014, 16, 4126-4129 |
1517254 | CIF | C22 H25 N3 O2 | P b c a | 11.1623; 13.076; 27.158 90; 90; 90 | 3963.9 | Galvez, Jaime; Castillo, Juan-Carlos; Quiroga, Jairo; Rajzmann, Michel; Rodriguez, Jean; Coquerel, Yoann Divergent Chemo-, Regio-, and Diastereoselective Normal Electron-Demand Povarov-Type Reactions with α-Oxo-ketene Dienophiles. Organic letters, 2014, 16, 4126-4129 |
1517265 | CIF | C30 H38 O6 | P 43 21 2 | 14.3442; 14.3442; 26.2596 90; 90; 90 | 5403.07 | Yang, Yong-Xun; Shan, Lei; Liu, Qing-Xin; Shen, Yun-Heng; Zhang, Jian-Ping; Ye, Ji; Xu, Xi-Ke; Li, Hui-Liang; Zhang, Wei-Dong Carpedilactones A-D, Four New Isomeric Sesquiterpene Lactone Dimers with Potent Cytotoxicity from Carpesium faberi. Organic letters, 2014, 16, 4216-4219 |
1517266 | CIF | C65 H87 N O14 | P 1 | 11.0003; 11.3149; 11.9224 88.459; 75.604; 82.956 | 1426.49 | Yang, Yong-Xun; Shan, Lei; Liu, Qing-Xin; Shen, Yun-Heng; Zhang, Jian-Ping; Ye, Ji; Xu, Xi-Ke; Li, Hui-Liang; Zhang, Wei-Dong Carpedilactones A-D, Four New Isomeric Sesquiterpene Lactone Dimers with Potent Cytotoxicity from Carpesium faberi. Organic letters, 2014, 16, 4216-4219 |
1517267 | CIF | C30 H38 O6 | P 21 21 21 | 8.4688; 9.616; 32.4284 90; 90; 90 | 2640.84 | Yang, Yong-Xun; Shan, Lei; Liu, Qing-Xin; Shen, Yun-Heng; Zhang, Jian-Ping; Ye, Ji; Xu, Xi-Ke; Li, Hui-Liang; Zhang, Wei-Dong Carpedilactones A-D, Four New Isomeric Sesquiterpene Lactone Dimers with Potent Cytotoxicity from Carpesium faberi. Organic letters, 2014, 16, 4216-4219 |
1517268 | CIF | C30 H40 O7 | P 1 21 1 | 11.9866; 7.7683; 14.6557 90; 110.8; 90 | 1275.73 | Yang, Yong-Xun; Shan, Lei; Liu, Qing-Xin; Shen, Yun-Heng; Zhang, Jian-Ping; Ye, Ji; Xu, Xi-Ke; Li, Hui-Liang; Zhang, Wei-Dong Carpedilactones A-D, Four New Isomeric Sesquiterpene Lactone Dimers with Potent Cytotoxicity from Carpesium faberi. Organic letters, 2014, 16, 4216-4219 |
1517269 | CIF | C16 H24 O3 | P -1 | 6.6062; 9.7077; 11.6325 95.271; 103.669; 93.602 | 719.05 | Handore, Kishor L.; Reddy, D. Srinivasa Total synthesis of (±)-nardoaristolone B and its analogues. Organic letters, 2014, 16, 4252-4255 |
1517282 | CIF | C27 H32 F3 N O3 | C 1 2 1 | 27.7938; 6.3604; 18.1051 90; 127.987; 90 | 2522.6 | Han, Zhengxu S.; Xu, Yibo; Fandrick, Daniel R.; Rodriguez, Sonia; Li, Zhibin; Qu, Bo; Gonnella, Nina C.; Sanyal, Sanjit; Reeves, Jonathan T.; Ma, Shengli; Grinberg, Nelu; Haddad, Nizar; Krishnamurthy, Dhileep; Song, Jinhua J.; Yee, Nathan K.; Pfrengle, Waldemar; Ostermeier, Markus; Schnaubelt, Jürgen; Leuter, Zeno; Steigmiller, Sonja; Däubler, Jürgen; Stehle, Emanuel; Neumann, Lukas; Trieselmann, Thomas; Tielmann, Patrick; Buba, Annette; Hamm, Rainer; Koch, Gunter; Renner, Svenja; Dehli, Juan R.; Schmelcher, Florian; Stange, Christian; Mack, Jürgen; Soyka, Rainer; Senanayake, Chris H. Facile entry to an efficient and practical enantioselective synthesis of a polycyclic cholesteryl ester transfer protein inhibitor. Organic letters, 2014, 16, 4142-4145 |
1517283 | CIF | C21 H29 N O2 Si | P 1 21/c 1 | 14.9925; 10.25; 14.5255 90; 114.65; 90 | 2028.8 | Si, Chang-Mei; Huang, Wei; Du, Zhen-Ting; Wei, Bang-Guo; Lin, Guo-Qiang Diastereoconvergent Synthesis of trans-5-Hydroxy-6-Substituted-2-Piperidinones by Addition-Cyclization-Deprotection Process. Organic letters, 2014, 16, 4328-4331 |
1517284 | CIF | C22 H17 Br N2 O3 | P 21 21 21 | 7.37972; 14.8985; 16.3419 90; 90; 90 | 1796.74 | Ransborg, Lars Krogager; Overgaard, Mette; Hejmanowska, Joanna; Barfüsser, Sebastian; Jørgensen, Karl Anker; Albrecht, Lukasz Asymmetric Formation of Bridged Benzoxazocines through an Organocatalytic Multicomponent Dienamine-Mediated One-Pot Cascade. Organic letters, 2014, 16, 4182-4185 |
1517385 | CIF | C21 H22 Cl N O5 | P 1 21/n 1 | 11.0367; 9.0626; 19.1081 90; 98.327; 90 | 1891.07 | Cleary, Leah; Pitzen, Jennifer; Brailsford, John A.; Shea, Kenneth J. Progress toward the Total Synthesis of N-Methylwelwitindolinone B Isothiocyanate. Organic letters, 2014, 16, 4460 |
1517386 | CIF | C22 H27 N O5 | P -1 | 9.6052; 14.5858; 14.9637 67.5035; 80.6214; 86.2284 | 1910.97 | Cleary, Leah; Pitzen, Jennifer; Brailsford, John A.; Shea, Kenneth J. Progress toward the Total Synthesis of N-Methylwelwitindolinone B Isothiocyanate. Organic letters, 2014, 16, 4460 |
1517387 | CIF | C13 H18 O2 | P -1 | 7.4167; 8.783; 9.1296 104.251; 98.7965; 110.147 | 522.34 | Roosen, Philipp C.; Vanderwal, Christopher D. Investigations into an Anionic Oxy-Cope/Transannular Conjugate Addition Approach to 7,20-Diisocyanoadociane. Organic letters, 2014, 16, 4368 |
1517388 | CIF | C18 H26 O2 | P 1 21/c 1 | 8.5541; 8.9646; 20.1698 90; 101.772; 90 | 1514.2 | Roosen, Philipp C.; Vanderwal, Christopher D. Investigations into an Anionic Oxy-Cope/Transannular Conjugate Addition Approach to 7,20-Diisocyanoadociane. Organic letters, 2014, 16, 4368 |
1517389 | CIF | C18 H26 O2 | P 1 21/c 1 | 5.9268; 33.959; 7.8335 90; 105.164; 90 | 1521.7 | Roosen, Philipp C.; Vanderwal, Christopher D. Investigations into an Anionic Oxy-Cope/Transannular Conjugate Addition Approach to 7,20-Diisocyanoadociane. Organic letters, 2014, 16, 4368 |
1517390 | CIF | C22 H18 B2 F8 N2 | P b c n | 22.1736; 8.6842; 10.5294 90; 90; 90 | 2027.54 | Zhang, Xiaoping; Clennan, Edward L.; Arulsamy, Navamoney Photophysical and Electrochemical Characterization of a Helical Viologen, N,N'-Dimethyl-5,10-diaza[5]helicene. Organic letters, 2014, 16, 4610 |
1517391 | CIF | C23 H17 N O | P 1 21/c 1 | 9.1194; 26.295; 7.2648 90; 99.144; 90 | 1719.9 | Gao, Qinghe; Liu, Shan; Wu, Xia; Wu, Anxin Povarov-Type Reaction Using Methyl as New Input: Direct Synthesis of Substituted Quinolines by I2-Mediated Formal [3 + 2 + 1] Cycloaddition. Organic letters, 2014, 16, 4582 |
1517392 | CIF | C17 H18 Br N O3 S | C 1 2/c 1 | 26.156; 16.7699; 15.5605 90; 106.958; 90 | 6528.6 | Evans, P. Andrew; Burnie, Andrew J.; Negru, Daniela E. Rhodium-Catalyzed [(3+2)+1] Carbocyclization Reactions of Alkynylidenecyclopropanes with Carbon Monoxide: Regiospecific Construction of Polysubstituted Phenols. Organic letters, 2014, 16, 4356 |
1517393 | CIF | C26 H20 Br Cl N2 O2 S | P -1 | 9.6181; 11.3853; 11.4584 96.403; 92.318; 109.423 | 1171.93 | Kiruthika, Selvarangam E.; Nandakumar, Avanashiappan; Perumal, Paramasivan Thirumalai Synthesis of Pyrrolo-/Indolo[1,2-a]quinolines and Naphtho[2,1-b]thiophenes from gem-Dibromovinyls and Sulphonamides. Organic letters, 2014, 16, 4424 |
1517394 | CIF | C15 H26 O6 | P 21 21 21 | 8.7271; 10.0996; 18.599 90; 90; 90 | 1639.3 | Wu, Yi-Biao; Tang, Yu; Luo, Guo-Ying; Chen, Yang; Hsung, Richard P. An Approach toward Constructing the Trioxadispiroketal Core in the DEF-Ring of (+)-Spirastrellolide A. Organic letters, 2014, 16, 4550 |
1517395 | CIF | C27 H22 Cl2 O3 | P -1 | 9.881; 10.831; 11.457 97.91; 101.73; 98.44 | 1169.6 | Liang, Renxiao; Ma, Tongmei; Zhu, Shifa Silver-Catalyzed Reaction of Enynals with Alkenes: A Tandem 1,3-Dipolar Cycloaddition/Cyclopropanation. Organic letters, 2014, 16, 4412 |
1517396 | CIF | C13 H15 N O3 | P -1 | 10.7856; 11.0756; 12.1131 69.1857; 65.3217; 63.0462 | 1147.1 | Slater, Natasha H.; Brown, Natalie J.; Elsegood, Mark R. J.; Kimber, Marc C. The Au(I) Catalyzed Activation of Allenamides and Their Subsequent Transformation into Chromanes: A Method for the Regiocontrolled Addition to the α- and γ-Positions of the Allene Unit. Organic letters, 2014, 16, 4606 |
1517397 | CIF | C17 H23 N O4 | P 1 21/c 1 | 14.2303; 9.9756; 11.3012 90; 99.263; 90 | 1583.35 | David, Jonathan G.; Bai, Wen-Ju; Weaver, Marisa G.; Pettus, Thomas R. R. A General Diastereoselective Catalytic Vinylogous Aldol Reaction Among Tetramic Acid-Derived Pyrroles. Organic letters, 2014, 16, 4384 |
1517398 | CIF | C16 H14 O5 | P 1 21/c 1 | 10.1392; 6.5215; 22.148 90; 99.666; 90 | 1443.7 | Zhang, Zeguang; Jiang, Xuefeng Oxidative Coupling of Terminal Alkyne with α-Hydroxy Ketone: An Expedient Approach toward Ynediones. Organic letters, 2014, 16, 4400 |
1517399 | CIF | C15 H19 N O3 Si | P 1 21/c 1 | 11.6235; 10.0558; 16.1897 90; 127.493; 90 | 1501.41 | Liu, Shasha; Zhao, Jinbo; Kaminsky, Lauren; Wilson, Robert J.; Marino, Nadia; Clark, Daniel A. Ethylene Transposition: Ruthenium Hydride Catalyzed Intramolecular trans-Silylvinylation of Internal Alkynes. Organic letters, 2014, 16, 4456 |
1517400 | CIF | C15 H19 N O3 Si | P 1 21/c 1 | 11.6235; 10.0558; 18.5574 90; 136.196; 90 | 1501.41 | Liu, Shasha; Zhao, Jinbo; Kaminsky, Lauren; Wilson, Robert J.; Marino, Nadia; Clark, Daniel A. Ethylene Transposition: Ruthenium Hydride Catalyzed Intramolecular trans-Silylvinylation of Internal Alkynes. Organic letters, 2014, 16, 4456 |
1517401 | CIF | C15 H19 N O3 Si | P 1 21/n 1 | 11.6235; 10.0558; 12.9667 90; 97.843; 90 | 1501.42 | Liu, Shasha; Zhao, Jinbo; Kaminsky, Lauren; Wilson, Robert J.; Marino, Nadia; Clark, Daniel A. Ethylene Transposition: Ruthenium Hydride Catalyzed Intramolecular trans-Silylvinylation of Internal Alkynes. Organic letters, 2014, 16, 4456 |
1517402 | CIF | C24.25 H21.5 Br Cl0.5 O4 | P -1 | 11.2333; 13.7701; 15.8106 115.076; 103.332; 92.587 | 2126.93 | Mariaule, Gaëlle; Newsome, Gregory; Toullec, Patrick Y.; Belmont, Philippe; Michelet, Véronique Silver-Catalyzed Domino Hydroarylation/Cycloisomerization Reactions of ortho-Alkynylbenzaldehydes: An Entry to Functionalized Isochromene Derivatives. Organic letters, 2014, 16, 4570 |
1517412 | CIF | C27 H26 Br N O5 | P 1 21/c 1 | 9.8508; 26.583; 19.2662 90; 98.518; 90 | 4989.5 | Ma, Guan-Hua; Jiang, Bo; Tu, Xing-Jun; Ning, Yi; Tu, Shu-Jiang; Li, Guigen Synthesis of Isocoumarins with Different Substituted Patterns via Passerini-Aldol Sequence. Organic letters, 2014, 16, 4504 |
1517413 | CIF | C21 H20 Br N O5 | P 1 21/c 1 | 17.6201; 6.508; 17.6402 90; 91.731; 90 | 2021.9 | Ma, Guan-Hua; Jiang, Bo; Tu, Xing-Jun; Ning, Yi; Tu, Shu-Jiang; Li, Guigen Synthesis of Isocoumarins with Different Substituted Patterns via Passerini-Aldol Sequence. Organic letters, 2014, 16, 4504 |
1517415 | CIF | C24 H26 N6 | P -1 | 7.468; 7.906; 8.99 94.02; 100.02; 104.01 | 503.6 | Gregoliński, Janusz; Slepokura, Katarzyna; Paćkowski, Tomasz; Lisowski, Jerzy Expansion of a 2 + 2 Macrocycle into a 6 + 6 Macrocycle: Template Effect of Cadmium(II). Organic letters, 2014, 16, 4372 |
1517416 | CIF | C54 H58 N12 | P 42/n | 14.657; 14.657; 11.492 90; 90; 90 | 2468.8 | Gregoliński, Janusz; Slepokura, Katarzyna; Paćkowski, Tomasz; Lisowski, Jerzy Expansion of a 2 + 2 Macrocycle into a 6 + 6 Macrocycle: Template Effect of Cadmium(II). Organic letters, 2014, 16, 4372 |
1517417 | CIF | C72 H166 Cl12 N18 O26 | P -1 | 12.074; 15.164; 17.95 114.14; 90.19; 113.39 | 2698.2 | Gregoliński, Janusz; Slepokura, Katarzyna; Paćkowski, Tomasz; Lisowski, Jerzy Expansion of a 2 + 2 Macrocycle into a 6 + 6 Macrocycle: Template Effect of Cadmium(II). Organic letters, 2014, 16, 4372 |
1517418 | CIF | C76 H144 Cl12 N20 O12 | P -1 | 14.379; 14.999; 15.291 78.08; 86.71; 61.81 | 2841 | Gregoliński, Janusz; Slepokura, Katarzyna; Paćkowski, Tomasz; Lisowski, Jerzy Expansion of a 2 + 2 Macrocycle into a 6 + 6 Macrocycle: Template Effect of Cadmium(II). Organic letters, 2014, 16, 4372 |
1517419 | CIF | C16 H16 Cl N O4 | P 1 21 1 | 6.0935; 8.9206; 14.327 90; 100.014; 90 | 766.9 | Liu, Kang; Teng, Huai-Long; Wang, Chun-Jiang Et3N-Catalyzed Tandem Formal [4 + 3] Annulation/Decarboxylation/Isomerization of Methyl Coumalate with Imine Esters: Access to Functionalized Azepine Derivatives. Organic letters, 2014, 16, 4508 |
1517420 | CIF | C27 H20 Br Cl F3 N3 O4 | P 21 21 21 | 8.7054; 15.5955; 38.4153 90; 90; 90 | 5215.5 | Zhao, Mei-Xin; Bi, Hong-Lei; Jiang, Rong-Hui; Xu, Xu-Wei; Shi, Min Cinchona Alkaloid Squaramide/AgOAc Cooperatively Catalyzed Diastereo- and Enantioselective Mannich/Cyclization Cascade Reaction of Isocyanoacetates and Cyclic Trifluoromethyl Ketimines. Organic letters, 2014, 16, 4566 |
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