(PDF) 7,7-Dimethyltricyclo[3.3.0.02,8]octan-3-Ones as

7,7-Dimethyltricyclo[3.3.0.02,8]octan-3-Ones as Synthetic Intermediates. IV. A Further Examination of Cyclopropane Ring Opening in the Tricyclo[3.3.0.02,8]octan-3-One System.

Chemical and Pharmaceutical Bulletin - Japan

doi 10.1248/cpb.37.3114

Full Text

Open PDF

Abstract

Available in full text

Date

January 1, 1989

Authors

Publisher

Pharmaceutical Society of Japan

Related search

7,7-Dimethyltricyclo[3.3.0.02.8]octan-3-Ones as Synthetic Intermediates. II. A Total Synthesis of (.+-.)-Pentalenene, an Angular Triquinane Sesquiterpene.

Chemical and Pharmaceutical Bulletin

English

(1r,5s,8r)-1,8-Dihydroxy-6-Oxa-3-Azabicyclo[3.2.1]octan-2-One

Acta Crystallographica Section E Structure Reports Online

2004

English

Tricyclo[3.3.0.02,8]octanones as Building Blocks in Natural Products Synthesis. –Synthesis of (±)-Forsythide Aglycon Dimethyl Ester–

Chemistry Letters

Chemistry

1982

English

A New Reaction of a 7,7-Diethoxybicyclo[4.2.0]octan-2-One Derivative. The Formation of the Bicyclo[3.2.1]octane Skeleton

Bulletin of the Chemical Society of Japan

Chemistry

1980

English

1,3-Dichloroacetone as a Cyclopropanone Equivalent: 5-Oxaspiro[3.4]octan-1-One

Organic Syntheses

Organic Chemistry

Theoretical Chemistry

Physical

2007

English

Synthetic Photochemistry. XLI. Photorearrangement of 5-Alykyl-1-Hydroxy-8-Oxabicyclo[3.2.1]octa-3,6-Dien-2-Ones to 2-Alkyl-3-Oxatricyclo[3.3.0.02,8]octane-4,6-Diones

Bulletin of the Chemical Society of Japan

Chemistry

1988

English

Structures of the Intermediates Formed in the Ring-Opening Reaction of 2-Chloro-3-Nitropyridine

English

Structures of the Intermediates Formed in the Ring-Opening Reaction of 2-Chloro-3-Nitropyridine

English

Synthetic Study on Gymnomitrol and Related Compounds. I. Preparation and Cyclopropane Ring Opening of 1,2,6-Trimethyltetracyclo(5.3.1.02,6.08,11)undecan-9-One.

Chemical and Pharmaceutical Bulletin

English

Amanote Research

7,7-Dimethyltricyclo[3.3.0.02,8]octan-3-Ones as Synthetic Intermediates. IV. A Further Examination of Cyclopropane Ring Opening in the Tricyclo[3.3.0.02,8]octan-3-One System.

Chemical and Pharmaceutical Bulletin - Japan

doi 10.1248/cpb.37.3114

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

7,7-Dimethyltricyclo[3.3.0.02.8]octan-3-Ones as Synthetic Intermediates. II. A Total Synthesis of (.+-.)-Pentalenene, an Angular Triquinane Sesquiterpene.

(1r,5s,8r)-1,8-Dihydroxy-6-Oxa-3-Azabicyclo[3.2.1]octan-2-One

Tricyclo[3.3.0.02,8]octanones as Building Blocks in Natural Products Synthesis. –Synthesis of (±)-Forsythide Aglycon Dimethyl Ester–

A New Reaction of a 7,7-Diethoxybicyclo[4.2.0]octan-2-One Derivative. The Formation of the Bicyclo[3.2.1]octane Skeleton

1,3-Dichloroacetone as a Cyclopropanone Equivalent: 5-Oxaspiro[3.4]octan-1-One

Synthetic Photochemistry. XLI. Photorearrangement of 5-Alykyl-1-Hydroxy-8-Oxabicyclo[3.2.1]octa-3,6-Dien-2-Ones to 2-Alkyl-3-Oxatricyclo[3.3.0.02,8]octane-4,6-Diones

Structures of the Intermediates Formed in the Ring-Opening Reaction of 2-Chloro-3-Nitropyridine

Structures of the Intermediates Formed in the Ring-Opening Reaction of 2-Chloro-3-Nitropyridine

Synthetic Study on Gymnomitrol and Related Compounds. I. Preparation and Cyclopropane Ring Opening of 1,2,6-Trimethyltetracyclo(5.3.1.02,6.08,11)undecan-9-One.