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Toward a total synthesis of an aglycone of spiramycin; preparation of a C-10/C-15 fragment

✍ Scribed by G. Oddon; D. Uguen

Book ID: 108386515
Publisher: Elsevier Science
Year: 1998
Tongue: French
Weight: 251 KB
Volume: 39
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(97)83164-4

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Toward a total synthesis of an aglycone

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Both homochiral acetates 4d and 5f, which were obtained by lipase-catalysed acetylation of either the tetraol 4a or the diol 5e, respectively, have been converted stereoconvergently into a C-5/C-9 fragment of the title antibiotic.

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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 “Full Text” option. The original article is trackable v

Toward a total synthesis of an aglycone

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