Stereoselective Synthesis of Steroid Side Chain: Synthesis of (2R∗,3R∗)-2-Methyl-3-[(1R∗)-1,5-Dimethylhexyl]Cyclopentanone
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397918508063834
Reference11 articles.
1. Various approaches to the construction of aliphatic side chains of steroids and related compounds
2. A stereocontrolled approach toward vitamin D metabolites. A synthesis of the Inhoffen-Lythgoe diol
3. Stereochemistry of the nucleophilic ring-opening of activated bicyclo-[3.1.0]Hexanes.
4. STEREOSELECTIVE TOTAL SYNTHESES OF (±)- AND OPTICALLY ACTIVE DEHYDROIRIDODIOLS
5. Previously, the synthesis of (+)-6and optically active cyclopentanone (3) has been achieved by two groups via the stereospecific routes, respectively
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3. Homoconjugate Addition of Organocuprate to Activated Cyclopropane and Its Application to the Synthesis of (±)-Juvabione;Bioscience, Biotechnology, and Biochemistry;1995-01
4. Synthetic Studies of Biologically Active Natural Products Using the Cleavage Reaction of Cyclopropane Ring.;Journal of Synthetic Organic Chemistry, Japan;1993
5. STEREOSELECTIVE SYNTHESES OF STEROID SIDE CHAINS. EFFICIENT SYNTHESES OF (2RS,3RS)-2-METHYL-3-[(1RS)-1,5-DIMETHYLHEXYL]CYCLOPENTANONE AND (2RS)-2-[(1RS)-3-OXOCYCLOHEXYL]PROPANOIC ACID;Chemistry Letters;1986-05-05
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