✦ LIBER ✦

A formal total synthesis of deoxybouvardin

✍ Scribed by Antony Bigot; René Beugelmans; Jieping Zhu

Book ID: 108378697
Publisher: Elsevier Science
Year: 1997
Tongue: French
Weight: 701 KB
Volume: 53
Category: Article
ISSN: 0040-4020
DOI: 10.1016/s0040-4020(97)00706-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Formal Total Synt

ChemInform Abstract: A Formal Total Synthesis of Deoxybouvardin.

✍ A. BIGOT; R. BEUGELMANS; J. ZHU 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

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.

A formal total synthesis of dactylol

✍ Leo A. Paquette; Won Hun Ham; David S. Dime 📂 Article 📅 1985 🏛 Elsevier Science 🌐 French ⚖ 247 KB

SWll7TlU~: The tetracyclic epoxide 16 was prepared in stereocontrolled fashion from 4,4dimethylcyclohexanone, the key steps being Saegusa ring expansion of its silyl enol ether

A formal total synthesis of geneserine

✍ Colin Wright; Madeline Shulkind; Keith Jones; Mervyn Thompson 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 140 KB

## Summay: The key oxindole intermediate (2) which has recently been used in a total synthesis of the alkaloid geneserine, has been prepared by a short, efficient route utilising a radical cyclisation.