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ent-(8S,10R)-15,16-Epoxy-19-norcleroda-4,11,13(16),14-tetraene-18,6(R):20,12-diolactone (isocrotocaudin)

โœ Scribed by Said, Ikram M. ;Noor, Ainal F. A. ;Syah, Yana M. ;Latif, Jalifah ;Ngah, Nurziana ;Yamin, Bohari M.


Book ID
104483747
Publisher
International Union of Crystallography
Year
2005
Tongue
English
Weight
197 KB
Volume
61
Category
Article
ISSN
1600-5368

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โœฆ Synopsis


The title compound, C 19 H 18 O 5 , is a diastereoisomer of crotocaudin, both being isolated from the plants of genus Croton. In isocrotocaudin, the furan moiety makes a dihedral angle with the adjacent lactone of 13.53 (17) . The cyclohexyl ring of the diterpene moiety adopts a chair confirmation. The weak intermolecular C-Hร ร รO hydrogen bonds link the molecules into linear chains along the c axis.


๐Ÿ“œ SIMILAR VOLUMES


(1R,4S,8R,12S,13S,14R,16S,17R,19R)-14-Hy
โœ Shi, Hao ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› International Union of Crystallography ๐ŸŒ English โš– 963 KB

The title compound, C~22~H~28~O~8~, was prepared from the natural diterpenoid macrocalyxin J by two steps. It is built up from five fused rings: three six-membered rings and two five-membered rings. Two molecules are present in the asymmetric unit; both independent molecules have the same absolute c

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โ€œFull Textโ€ option. The original article is trackable v