𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of campesteryl acetate ((24R)-24-methyl-3β-acetoxycholesten-5-ene) and its 24S-epimer

✍ Scribed by R. Ikan; A. Markus; E.D. Bergmann

Book ID
119481204
Publisher
Elsevier Science
Year
1970
Tongue
English
Weight
265 KB
Volume
16
Category
Article
ISSN
0039-128X

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Stereoselective synthesis of (22R, 23R,
Stereoselective synthesis of (22R, 23R, 24S)-3β-hydroxy-5-ene-22,23-dihydroxy-24-methyl-cholestane: A brassinolide intermediate from 16-dehydropregnenolone acetate.
✍ Braja G. Hazra; Padmakar L. Joshi; Bharat B. Bahule; Narshinha P. Argade; Vandan 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 760 KB

## Abstnzck: A new synthesis of the important aldehyde I torn easily available l&Dehydropregnenolone acetate (I6-DPA) in high yield is described. The aidehyde I ip converted to trio1 24, involving a stereaselective generation of all the four chiral centers in the brassinolide side chain. The importa

Synthesis of the putative marine sterols
Synthesis of the putative marine sterols [24R]- and [24S]-23,24-dimethyl-5α-cholest-23(29)-en-3β-ol.
✍ T. Gebreyesus; Carl Djerassi 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 207 KB

The synthesis and stereochemistry of [24R]-and [24S]-23,24-dimethyl-5c+cholest-23(29)-en-3B-ol is reported; both isomers are different from a natural marine sterol to which the structure had been assigned. and Dr. M. Alam (University of Houston) for a sample of the G. monilata sterol.