✦ LIBER ✦

A formal total synthesis of (±)-strigol

✍ Scribed by Ulrich Berlage; Jürgen Schmidt; Ulrike Peters; Peter Welzel

Book ID: 108382997
Publisher: Elsevier Science
Year: 1987
Tongue: French
Weight: 263 KB
Volume: 28
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)96293-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A (formal) total synthesis of (+) - stri

A (formal) total synthesis of (+) - strigol, the witchweed germination factor

✍ Ulrich Berlage; Jürgen Schmidt; Zenka Milkova; Peter Welzel 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 263 KB

Practical total synthesis of (.+-.)-stri

Practical total synthesis of (.+-.)-strigol

✍ Brooks, Dee W.; Bevinakatti, H. S.; Kennedy, Eileen; Hathaway, Jim 📂 Article 📅 1985 🏛 American Chemical Society 🌐 English ⚖ 668 KB

Total synthesis of d1-strigol

✍ Heather, J. B.; Mittal, R. S. D.; Sih, Charles J. 📂 Article 📅 1974 🏛 American Chemical Society 🌐 English ⚖ 257 KB

A formal total synthesis of (±)-aphidico

A formal total synthesis of (±)-aphidicolin

✍ Steven P. Tanis; Yu-Hwey Chuang; David B. Head 📂 Article 📅 1985 🏛 Elsevier Science 🌐 French ⚖ 211 KB

A formal total synthesis of (-)-isoavena

A formal total synthesis of (-)-isoavenaciolide

✍ Chriss E McDonald; Robert W Dugger 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 193 KB

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.