✦ LIBER ✦

A formal total synthesis of (.+-.)-laurenene

✍ Scribed by Paquette, Leo A.; Okazaki, Mark E.; Caille, Jean Claude

Book ID: 120880601
Publisher: American Chemical Society
Year: 1988
Tongue: English
Weight: 709 KB
Volume: 53
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00238a003

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Intramolecular photocycloaddition-cyclob

Intramolecular photocycloaddition-cyclobutane fragmentation: total synthesis of (.+-.)-laurenene

✍ Crimmins, Michael T.; Gould, Lori D. 📂 Article 📅 1987 🏛 American Chemical Society 🌐 English ⚖ 298 KB

Synthetic studies on arene-olefin cycloa

Synthetic studies on arene-olefin cycloadditions. 10. A concise, stereocontrolled total synthesis of (.+-.)-laurenene

✍ Wender, Paul A.; Von Geldern, Thomas W.; Levine, Barry H. 📂 Article 📅 1988 🏛 American Chemical Society 🌐 English ⚖ 409 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.

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