Crystallography Open Database
Search results
Result: there are 837 entries in the selection
Switch to the old layout of the pageDownload all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)
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; DobrzaĆska, 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 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!

