Crystallography Open Database
Search results
Result: there are 475 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 & biomolecular chemistry' volume of publication is 11
COD ID ![]() |
Links | Formula ![]() |
Space group ![]() |
Cell parameters | Cell volume ![]() |
Bibliography |
---|---|---|---|---|---|---|
7152838 | CIF | C22 H22 O8 | P 1 21 1 | 6.69; 7.08; 20.692 90; 95.955; 90 | 974.8 | Wang, Zhaofeng; Zhao, Kun; Fu, Junkai; Zhang, Junlin; Yin, Weiyu; Tang, Yefeng Organocatalytic 1,4-conjugate addition of ascorbic acid to α,β-unsaturated aldehydes: bio-inspired total syntheses of leucodrin, leudrin and proposed structure of dilaspirolactone. Organic & biomolecular chemistry, 2013, 11, 2093-2097 |
7152839 | CIF | C15 H15 N O4 | P 1 21/n 1 | 6.1123; 17.974; 11.7487 90; 96.038; 90 | 1283.58 | Zhang, Jinzhu; Wu, Jing; Yin, Zhiwei; Zeng, Haisu; Khanna, Kunal; Hu, Chunhua; Zheng, Shengping An expedient stereoselective and chemoselective synthesis of bicyclic oxazolidinones from quinols and isocyanates. Organic & biomolecular chemistry, 2013, 11, 2939-2942 |
7152840 | CIF | C15 H14 Br N O3 | P 1 21/c 1 | 11.3435; 5.9481; 20.6935 90; 103.511; 90 | 1357.6 | Zhang, Jinzhu; Wu, Jing; Yin, Zhiwei; Zeng, Haisu; Khanna, Kunal; Hu, Chunhua; Zheng, Shengping An expedient stereoselective and chemoselective synthesis of bicyclic oxazolidinones from quinols and isocyanates. Organic & biomolecular chemistry, 2013, 11, 2939-2942 |
7152841 | CIF | C16 H17 N O3 | P 1 21/c 1 | 14.8275; 7.8956; 11.8515 90; 94.993; 90 | 1382.2 | Zhang, Jinzhu; Wu, Jing; Yin, Zhiwei; Zeng, Haisu; Khanna, Kunal; Hu, Chunhua; Zheng, Shengping An expedient stereoselective and chemoselective synthesis of bicyclic oxazolidinones from quinols and isocyanates. Organic & biomolecular chemistry, 2013, 11, 2939-2942 |
7152842 | CIF | C18 H18 O2 | P 1 21/n 1 | 8.517; 10.598; 16.662 90; 94.57; 90 | 1499.2 | Zhang, Jian-Jian; Yan, Chang-Song; Peng, Yu; Luo, Zhen-Biao; Xu, Xiao-Bo; Wang, Ya-Wen Total synthesis of (±)-sacidumlignans D and A through Ueno-Stork radical cyclization reaction. Organic & biomolecular chemistry, 2013, 11, 2498-2513 |
7152843 | CIF | C22 H24 O6 | P 1 2/c 1 | 12.3947; 8.5143; 21.6771 90; 104.571; 90 | 2214.1 | Zhang, Jian-Jian; Yan, Chang-Song; Peng, Yu; Luo, Zhen-Biao; Xu, Xiao-Bo; Wang, Ya-Wen Total synthesis of (±)-sacidumlignans D and A through Ueno-Stork radical cyclization reaction. Organic & biomolecular chemistry, 2013, 11, 2498-2513 |
7152844 | CIF | C22 H28 O7 | C 1 2/c 1 | 12.701; 13.483; 24.743 90; 95.229; 90 | 4220 | Zhang, Jian-Jian; Yan, Chang-Song; Peng, Yu; Luo, Zhen-Biao; Xu, Xiao-Bo; Wang, Ya-Wen Total synthesis of (±)-sacidumlignans D and A through Ueno-Stork radical cyclization reaction. Organic & biomolecular chemistry, 2013, 11, 2498-2513 |
7152845 | CIF | C11 H13 N S Se | P 1 21/n 1 | 8.376; 13.152; 11.24 90; 104.024; 90 | 1201.3 | Toyoda, Yosuke; Ninomiya, Masayuki; Ebihara, Masahiro; Koketsu, Mamoru The Staudinger reaction with 2-imino-1,3-thiaselenanes toward the synthesis of C4 spiro-β-lactams. Organic & biomolecular chemistry, 2013, 11, 2652-2659 |
7152846 | CIF | C14 H17 N O2 S Se | P 1 21/c 1 | 12.348; 17.281; 14.35 90; 100.9; 90 | 3006.8 | Toyoda, Yosuke; Ninomiya, Masayuki; Ebihara, Masahiro; Koketsu, Mamoru The Staudinger reaction with 2-imino-1,3-thiaselenanes toward the synthesis of C4 spiro-β-lactams. Organic & biomolecular chemistry, 2013, 11, 2652-2659 |
7152847 | CIF | C13 H15 N O2 S Se | P 1 21/n 1 | 12.283; 5.835; 19.052 90; 91.933; 90 | 1364.7 | Toyoda, Yosuke; Ninomiya, Masayuki; Ebihara, Masahiro; Koketsu, Mamoru The Staudinger reaction with 2-imino-1,3-thiaselenanes toward the synthesis of C4 spiro-β-lactams. Organic & biomolecular chemistry, 2013, 11, 2652-2659 |
7152848 | CIF | C33 H28 O4 | P 1 21/c 1 | 13.3763; 18.3674; 10.6707 90; 98.939; 90 | 2589.82 | Selvi, Thangavel; Srinivasan, Kannupal Indium triflate-catalysed Diels-Alder reactions of isochromenylium cations with enones. Organic & biomolecular chemistry, 2013, 11, 2162-2167 |
7152849 | CIF | C27 H43 N O4 | P 21 21 21 | 9.862; 10.08; 27.249 90; 90; 90 | 2708.8 | Shankar, Sreejith P.; Jagodzinska, Monika; Malpezzi, Luciana; Lazzari, Paolo; Manca, Ilaria; Greig, Iain R.; Sani, Monica; Zanda, Matteo Synthesis and structure-activity relationship studies of novel tubulysin U analogues - effect on cytotoxicity of structural variations in the tubuvaline fragment. Organic & biomolecular chemistry, 2013, 11, 2273-2287 |
7152850 | CIF | C17 H28 N2 O5 S | P 1 21/c 1 | 12.756; 15.696; 10.018 90; 98.51; 90 | 1983.7 | Shankar, Sreejith P.; Jagodzinska, Monika; Malpezzi, Luciana; Lazzari, Paolo; Manca, Ilaria; Greig, Iain R.; Sani, Monica; Zanda, Matteo Synthesis and structure-activity relationship studies of novel tubulysin U analogues - effect on cytotoxicity of structural variations in the tubuvaline fragment. Organic & biomolecular chemistry, 2013, 11, 2273-2287 |
7152851 | CIF | C29 H39 F6 N3 O8 | P 21 21 21 | 14.698; 14.698; 15.598 90; 90; 90 | 3369.7 | Bellucci, Maria Cristina; Terraneo, Giancarlo; Volonterio, Alessandro Multi-component synthesis of peptide-sugar conjugates. Organic & biomolecular chemistry, 2013, 11, 2421-2444 |
7152852 | CIF | C21 H35 F6 N3 O4 | P 1 21 1 | 11.13; 17.499; 14.051 90; 99.9; 90 | 2695.9 | Bellucci, Maria Cristina; Terraneo, Giancarlo; Volonterio, Alessandro Multi-component synthesis of peptide-sugar conjugates. Organic & biomolecular chemistry, 2013, 11, 2421-2444 |
7152853 | CIF | C11 H13 N O | P 1 21/n 1 | 7.192; 14.069; 9.2117 90; 102.365; 90 | 910.5 | Webber, Matthew J; Warren, Sarah A; Grainger, Damian M; Weston, Matthew; Clark, Stacy; Woodhead, Steven J; Powell, Lyn; Stokes, Stephen; Alanine, Alexander; Stonehouse, Jeffrey P; Frampton, Christopher S; White, Andrew J P; Spivey, Alan C Towards the enantioselective synthesis of (-)-euonyminol‒preparation of a fully functionalised lower-rim model. Organic & biomolecular chemistry, 2013, 11, 2514-2533 |
7152854 | CIF | C23 H27 N O4 | P 1 21 1 | 6.2151; 16.8252; 9.7311 90; 90.176; 90 | 1017.58 | Webber, Matthew J; Warren, Sarah A; Grainger, Damian M; Weston, Matthew; Clark, Stacy; Woodhead, Steven J; Powell, Lyn; Stokes, Stephen; Alanine, Alexander; Stonehouse, Jeffrey P; Frampton, Christopher S; White, Andrew J P; Spivey, Alan C Towards the enantioselective synthesis of (-)-euonyminol‒preparation of a fully functionalised lower-rim model. Organic & biomolecular chemistry, 2013, 11, 2514-2533 |
7152855 | CIF | C40 H47 N O7 | P -1 | 10.6749; 11.6338; 17.366 108.132; 103.266; 110.833 | 1769.5 | Webber, Matthew J; Warren, Sarah A; Grainger, Damian M; Weston, Matthew; Clark, Stacy; Woodhead, Steven J; Powell, Lyn; Stokes, Stephen; Alanine, Alexander; Stonehouse, Jeffrey P; Frampton, Christopher S; White, Andrew J P; Spivey, Alan C Towards the enantioselective synthesis of (-)-euonyminol‒preparation of a fully functionalised lower-rim model. Organic & biomolecular chemistry, 2013, 11, 2514-2533 |
7152856 | CIF | C19 H27 N O5 | P 43 | 16.17422; 16.17422; 7.32793 90; 90; 90 | 1917.03 | Webber, Matthew J; Warren, Sarah A; Grainger, Damian M; Weston, Matthew; Clark, Stacy; Woodhead, Steven J; Powell, Lyn; Stokes, Stephen; Alanine, Alexander; Stonehouse, Jeffrey P; Frampton, Christopher S; White, Andrew J P; Spivey, Alan C Towards the enantioselective synthesis of (-)-euonyminol‒preparation of a fully functionalised lower-rim model. Organic & biomolecular chemistry, 2013, 11, 2514-2533 |
7152857 | CIF | C19 H29 N O6 | P 1 21/c 1 | 10.6847; 12.1746; 14.678 90; 95.328; 90 | 1901.09 | Webber, Matthew J; Warren, Sarah A; Grainger, Damian M; Weston, Matthew; Clark, Stacy; Woodhead, Steven J; Powell, Lyn; Stokes, Stephen; Alanine, Alexander; Stonehouse, Jeffrey P; Frampton, Christopher S; White, Andrew J P; Spivey, Alan C Towards the enantioselective synthesis of (-)-euonyminol‒preparation of a fully functionalised lower-rim model. Organic & biomolecular chemistry, 2013, 11, 2514-2533 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!