Crystallography Open Database
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Searching journal of publication like 'Organic letters' volume of publication is 14
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1516064 | CIF | C15 H19 N O | I b a 2 | 10.9646; 34.3413; 6.972 90; 90; 90 | 2625.23 | Brawn, Ryan A.; Guimarães, Cristiano R W; McClure, Kim F.; Liras, Spiros An efficient synthesis of bridged heterocycles from an Ir(I) bis-amination/ring-closing metathesis sequence. Organic letters, 2012, 14, 4802-4805 |
| 1516066 | CIF | C19 H25 N3 O2 | P 1 21/c 1 | 10.5786; 10.5791; 15.5501 90; 104.447; 90 | 1685.22 | Tan, Shen H.; Banwell, Martin G.; Willis, Anthony C.; Reekie, Tristan A. Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine. Organic letters, 2012, 14, 5621-5623 |
| 1516067 | CIF | C20 H29 N3 O2 | P 1 21/c 1 | 11.8836; 10.3003; 15.9702 90; 109.242; 90 | 1845.62 | Tan, Shen H.; Banwell, Martin G.; Willis, Anthony C.; Reekie, Tristan A. Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine. Organic letters, 2012, 14, 5621-5623 |
| 1516068 | CIF | C19 H26 N2 O | P n a 21 | 13.7232; 14.9269; 7.6655 90; 90; 90 | 1570.24 | Tan, Shen H.; Banwell, Martin G.; Willis, Anthony C.; Reekie, Tristan A. Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine. Organic letters, 2012, 14, 5621-5623 |
| 1516069 | CIF | C21 H38 O4 | P 21 21 21 | 5.2688; 7.4978; 52.786 90; 90; 90 | 2085.28 | Persich, Peter; Kerschbaumer, Julia; Helling, Sandra; Hildmann, Barbara; Wibbeling, Birgit; Haufe, Günter Transannular O-heterocyclization: a useful tool for the total synthesis of Murisolin and 16,19-cis-Murisolin. Organic letters, 2012, 14, 5628-5631 |
| 1516074 | CIF | C40 H41 N3 O4 | P -1 | 12.3712; 12.5383; 13.3489 102.471; 100.682; 118.295 | 1677.5 | Castellano, Teresa G.; Neo, Ana G.; Marcaccini, Stefano; Marcos, Carlos F. Enols as feasible acid components in the Ugi condensation. Organic letters, 2012, 14, 6218-6221 |
| 1516075 | CIF | C19 H24 N2 O3 | P 21 21 21 | 7.9485; 12.166; 17.196 90; 90; 90 | 1662.9 | Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J. The synthesis of melohenine B and a related natural product. Organic letters, 2012, 14, 6166-6169 |
| 1516076 | CIF | C20 H22 N2 O6 | P 21 21 21 | 7.1383; 10.9101; 23.798 90; 90; 90 | 1853.4 | Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J. The synthesis of melohenine B and a related natural product. Organic letters, 2012, 14, 6166-6169 |
| 1516077 | CIF | C21 H26 N2 O5 | P 61 | 8.268; 8.268; 48.704 90; 90; 120 | 2883.3 | Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J. The synthesis of melohenine B and a related natural product. Organic letters, 2012, 14, 6166-6169 |
| 1516078 | CIF | C21 H28 N2 O3 | P 21 21 21 | 7.4222; 9.96; 25.642 90; 90; 90 | 1895.6 | Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J. The synthesis of melohenine B and a related natural product. Organic letters, 2012, 14, 6166-6169 |
| 1516079 | CIF | C22 H26 N2 O4 | P 21 21 21 | 7.9567; 12.3012; 20.572 90; 90; 90 | 2013.5 | Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J. The synthesis of melohenine B and a related natural product. Organic letters, 2012, 14, 6166-6169 |
| 1516081 | CIF | C14 H17 B F2 N4 | P -1 | 7.3413; 7.5696; 13.1377 96.128; 99.18; 95.256 | 712.2 | Lee, Ho Yong; Olasz, András; Chen, Chun-Hsing; Lee, Dongwhan Three-stage binary switching of azoaromatic polybase. Organic letters, 2012, 14, 6286-6289 |
| 1516082 | CIF | C29 H20 N2 O7 | P -1 | 10.6771; 13.0878; 18.3378 83.667; 73.144; 75.898 | 2376.35 | Kelgtermans, Hans; Dobrzańska, Liliana; Van Meervelt, Luc; Dehaen, Wim A fragment-based approach toward substituted trioxa[7]helicenes. Organic letters, 2012, 14, 5200-5203 |
| 1516083 | CIF | C32 H38 O8 | P 1 21/c 1 | 6.0458; 9.8845; 24.023 90; 95.05; 90 | 1430 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516084 | CIF | C40 H54 O8 | P 1 21/c 1 | 16.6322; 9.1956; 12.1051 90; 98.357; 90 | 1831.73 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516085 | CIF | C26 H24 O8 | P 1 21/n 1 | 5.271; 14.1093; 15.2301 90; 94.765; 90 | 1128.7 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516086 | CIF | C24 H20 O8 | P 1 21/c 1 | 10.8267; 9.5361; 20.2199 90; 97.858; 90 | 2068 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516087 | CIF | C6 H5 Br O3 | P 1 21/n 1 | 10.3165; 4.9709; 14.1637 90; 101.925; 90 | 710.67 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516088 | CIF | C36 H42 O6 | C 1 2/c 1 | 29.11; 9.5418; 22.962 90; 103.062; 90 | 6212.9 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516089 | CIF | C32 H26 O8 | P 1 21/c 1 | 9.5983; 5.4838; 24.21 90; 91.793; 90 | 1273.7 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516090 | CIF | C26 H26 O8 | P 1 21/n 1 | 7.7228; 11.0389; 13.6925 90; 97.28; 90 | 1157.89 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516091 | CIF | C40 H52 O8 | P -1 | 5.7869; 9.9739; 16.9218 87.166; 81.47; 78.248 | 945.45 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516092 | CIF | C12 H12 Br2 O6 | P 1 21/n 1 | 9.6055; 7.7143; 18.8681 90; 93.576; 90 | 1395.4 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516093 | CIF | C40 H54 O12 | P -1 | 5.9676; 9.4094; 17.2733 89.735; 85.714; 85.834 | 964.7 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516094 | CIF | C32 H26 O8 | P -1 | 6.1693; 9.7194; 11.3573 67.533; 80.008; 86.414 | 619.77 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516095 | CIF | C32 H38 O12 | P -1 | 5.946; 10.5168; 12.6676 81.198; 80.39; 81.904 | 766.41 | Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core. Organic letters, 2012, 14, 1374-1377 |
| 1516097 | CIF | C11 H12 O5 | C 1 c 1 | 10.4253; 12.8651; 8.1381 90; 109.962; 90 | 1025.92 | Barradas, Silvia; Hernández-Torres, Gloria; Urbano, Antonio; Carreño, M Carmen Total synthesis of natural p-quinol cochinchinenone. Organic letters, 2012, 14, 5952-5955 |
| 1516099 | CIF | C23 H20 N2 O | P 1 21 1 | 6.4088; 17.279; 8.579 90; 101.67; 90 | 930.4 | Cai, Zhong-Jian; Wang, Shun-Yi; Ji, Shun-Jun CuI/BF3·Et2O cocatalyzed aerobic dehydrogenative reactions of ketones with benzylamines: facile synthesis of substituted imidazoles. Organic letters, 2012, 14, 6068-6071 |
| 1516100 | CIF | C22 H18 N2 | P 1 21/n 1 | 9.768; 11.392; 15.15 90; 97.216; 90 | 1672.5 | Cai, Zhong-Jian; Wang, Shun-Yi; Ji, Shun-Jun CuI/BF3·Et2O cocatalyzed aerobic dehydrogenative reactions of ketones with benzylamines: facile synthesis of substituted imidazoles. Organic letters, 2012, 14, 6068-6071 |
| 1516101 | CIF | C20 H18 O5 | P 1 21/n 1 | 16.4332; 5.5136; 18.3321 90; 106.549; 90 | 1592.2 | Truong, Phong; Shanahan, Charles S.; Doyle, Michael P. Divergent stereocontrol of acid catalyzed intramolecular aldol reactions of 2,3,7-triketoesters: synthesis of highly functionalized cyclopentanones. Organic letters, 2012, 14, 3608-3611 |
| 1516103 | CIF | C18 H24 N2 O | P b c n | 18.945; 8.6958; 20.3655 90; 90; 90 | 3355.1 | Zhao, Shu-Bin; Bilodeau, Eric; Lemieux, Valérie; Beauchemin, André M Hydrogen bonding directed intermolecular Cope-type hydroamination of alkenes. Organic letters, 2012, 14, 5082-5085 |
| 1516104 | CIF | C30 H28 Cl N O4 S | P -1 | 10.0293; 16.6704; 17.4029 70.567; 76.603; 78.855 | 2647.7 | Hu, Jian; Tian, Bing; Wu, Xinyan; Tong, Xiaofeng Tertiary amine-triggered cascade S(N)2/cycloaddition: an efficient construction of complex azaheterocycles under mild conditions. Organic letters, 2012, 14, 5074-5077 |
| 1516105 | CIF | C22 H26 N2 O6 | P 1 21/n 1 | 11.618; 12.024; 16.15 90; 110.574; 90 | 2112.2 | Villa, Reymundo A.; Xu, Qihai; Kwon, Ohyun Total synthesis of (±)-hirsutine: application of phosphine-catalyzed imine-allene [4 + 2] annulation. Organic letters, 2012, 14, 4634-4637 |
| 1556124 | CIF | C26 H30 I N O5 | P 21 21 21 | 7.7887; 14.737; 21.142 90; 90; 90 | 2426.7 | Ciesielski, Jennifer; Cariou, Kevin; Frontier, Alison J. A macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A. Organic letters, 2012, 14, 4082-4085 |
| 1556125 | CIF | C16 H19 N O5 | P 1 21 1 | 6.9621; 36.328; 6.9667 90; 117.642; 90 | 1560.9 | Ciesielski, Jennifer; Cariou, Kevin; Frontier, Alison J. A macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A. Organic letters, 2012, 14, 4082-4085 |
| 1556126 | CIF | C26 H28 N2 O4 S | P 21 21 21 | 9.6487; 12.0714; 19.866 90; 90; 90 | 2313.9 | Sequeira, Fatima C.; Chemler, Sherry R. Stereoselective synthesis of morpholines via copper-promoted oxyamination of alkenes. Organic letters, 2012, 14, 4482-4485 |
| 1556127 | CIF | C12 H12 O7 | P -1 | 7.8732; 7.9554; 9.7428 91.356; 108.391; 92.72 | 577.93 | Meck, Christine; Mohd, Noushad; Murelli, Ryan P. An oxidopyrylium cyclization/ring-opening route to polysubstituted α-hydroxytropolones. Organic letters, 2012, 14, 5988-5991 |
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