## Abstract The ^13^C‐labelled putative erythromycin biosynthetic intermediates, ((2__S__,3__S__,4__S__,5__R__,6__R__,7__R__)‐3,6,7‐trihydroxy‐2,4,6‐trimethyl[1‐^13^C]nonan‐5‐olide and __S__‐2‐acetylaminoethyl (2__R__,3__S__,4__S__,5__R__,6__S__,7__R__)‐3,5,6,7‐tetrahydroxy‐2,4,6‐trimethyl[1‐^13^C]
Carbohydrate-like chiral synthos. Preparation of (R) γ-hexanolide, (5R, 6S, 7S) 6,7-isopropylidendioxy-δ-octanolide and (+)-exobrevicomin from (2S, 3S, 4R) 2,3-isopropylidendioxy-4-benzyloxyhept-6-ene
✍ Scribed by Claudio Fuganti; Piero Grasselli; Giuseppe Pedrocchi-Fantoni; Stefano Servi; Carlo Zirotti
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 190 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The C 6' '7' C8 and C9 chiral products ( 8), ( 7), ( 14) and ( 19), containing one, two and three
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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
## Abstract The synthesis of sarcinaxanthin ((__2R,6R,2′R,6′R__)‐1), a symmetrical C~50~‐carotenoid with two γ‐end groups, isolated from __Sarcina lutea__ and from __Cellulomonas biazotea__ as major pigment, was based on the strategy C~20~ + C~10~ + C~20~ = C~50~ using camphoric acid as starting ma