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A formal total synthesis of (−)-brevisamide

✍ Scribed by Amos B. Smith III; Noriki Kutsumura; Justin Potuzak


Publisher
Elsevier Science
Year
2011
Tongue
French
Weight
444 KB
Volume
52
Category
Article
ISSN
0040-4039

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✦ Synopsis


A formal total synthesis of (-)-brevisamide has been achieved. The synthetic approach highlights a chemoselective asymmetric dihydroxylation and a one-pot Fraser-Reid epoxidation/PMB protection reaction sequence.


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A formal total synthesis of aplysiatoxin
✍ Hiroaki Okamura; Satoru Kuroda; Satoru Ikegami; Yoshio Ito; Tsutomu Katsuki; Mas 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 100 KB

A total synthesis of aplysiatoxin was achieved formally by construction of Kishi's intermediate 13 which carded all the stereochemislry required for the synthesis of aplysiatoxin, from four fragments described in the preceding communication.