✦ LIBER ✦

Development of New Chiral Building Blocks for Synthesis of Bicyclo[3.3.0]octane Compounds

✍ Scribed by Subburaj, Kandasamy; Okamoto, Sentaro; Sato, Fumie

Book ID: 118180099
Publisher: American Chemical Society
Year: 2002
Tongue: English
Weight: 51 KB
Volume: 67
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo016169s

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Chiral Building Blocks for the Synthesis

Chiral Building Blocks for the Synthesis of Triquinane Sesquiterpenes: Derivatives of 2-Methylbicyclo[3.3.0]octan-3-ol from Catalpol

✍ Prof. Dr. Klaus Weinges; Dipl.-Chem. Helene Iatridou; Dipl.-Chem. Hans-Georg Sta 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 285 KB

MCPBA oxidation of bicyclo[3.3.0]octane-

MCPBA oxidation of bicyclo[3.3.0]octane-3,7-dione: an easy entry to a new functionalized cyclopentanoid building block

✍ Luigi Garlaschelli; Giovanni Vidari; Giuseppe Zanoni 📂 Article 📅 1992 🏛 Elsevier Science 🌐 French ⚖ 594 KB

Diastereoselective synthesis of tricyclo

Diastereoselective synthesis of tricyclo[3.2.1.02,7]octanes; chiral building blocks for terpenes

✍ Norbert A. Braun; Iris Klein; Dietrich Spitzner; Bernhard Vogler; Horst Borrmann 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 188 KB

Total Synthesis of (-)-Dihydrocorynanthe

Total Synthesis of (-)-Dihydrocorynantheol (IV) Using Bicyclo[3.2.1]octenone Chiral Building Block (I).

✍ Ayako Tosaka; Shinichiro Ito; Norio Miyazawa; Masatoshi Shibuya; Kunio Ogasawara 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 19 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Synthesis of Oxazaphospholinobenzooxaaza

Synthesis of Oxazaphospholinobenzooxaazaphospholines and -oxadiazaphospholines—Compounds Having Pentacoordinated Phosphorus as Bridgehead of a Bicyclo [3.3.0]octane Skeleton

✍ Priv.-Doz. Dr. Alfred Schmidpeter; Josef Helmut Weinmaier 📂 Article 📅 1975 🏛 John Wiley and Sons 🌐 English ⚖ 197 KB

Enantioselective deprotonation of the mo

Enantioselective deprotonation of the monoacetals of bicyclo[3.3.0]octan-3,7-dione. An approach to the asymmetric synthesis of chiral synthons for carbacyclins

✍ Hiroyuki Izawa; Ryuichi Shirai; Hisashi Kawasaki; Hee-doo Kim; Kenji Koga 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 226 KB

Kinetic deprotonation of the monoacetals (4) of bicycloE3.3.0loctan-3,7-dione by chiral lithium amides (5) in the presence of excess trimethylsilyl chloride afforded the corresponding silyl enol ethers (6), useful synthons for the synthesis of optically active carbacyclins, in up to 94% ee.