Studies on the diastereoselective preparation of bis-cyclopropanes

Journal of Organic Chemistry

Volumn 61, Issue 25, 1996, Pages 8792-8798

  Theberge, Cory R ^a   Verbicky, Christopher A ^a   Zercher, Charles K ^a  

^a Univ of New Hampshire   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000104069     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo961235p     Document Type: Article

References (51)

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51. Methylene chloride was also used as a solvent in this reaction sequence. The yield of bis-cyclopropyl ester formation was slightly higher since none of the competing cycloheptatrienoate was formed. The stereoselectivity of the process was indistinguishable when moving between methylene chloride and benzene.