✦ LIBER ✦

Formal Total Synthesis of Spirangien A

✍ Scribed by Gregg, Claire; Gunawan, Christian; Ng, Audrey Wai Yi; Wimala, Samantha; Wickremasinghe, Sonali; Rizzacasa, Mark A.

Book ID: 118271742
Publisher: American Chemical Society
Year: 2013
Tongue: English
Weight: 716 KB
Volume: 15
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol3033253

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Total synthesis of (−)-spirangien A and

Total synthesis of (−)-spirangien A and its methyl ester

✍ Paterson, Ian; Findlay, Alison D.; Noti, Christian 📂 Article 📅 2008 🏛 Royal Society of Chemistry 🌐 English ⚖ 538 KB

ChemInform Abstract: Total Synthesis of

ChemInform Abstract: Total Synthesis of (-)-Spirangien A and Its Methyl Ester.

✍ Ian Paterson; Alison D. Findlay; Christian Noti 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 19 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