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Volumn , Issue 6, 1999, Pages 1063-1075

Stereoselective synthesis of cyclopropanes bearing adjacent stereocenters

Author keywords

Arene zinc interaction; Cyclopropanation; Diastereoselectivity; Hydroboration; Isopropenylcyclopropanes

Indexed keywords

CYCLOPROPANE DERIVATIVE;

EID: 0033061780     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-3507     Document Type: Article
Times cited : (25)

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    • The relative stereochemistry of 5a was assigned by comparaison with an authentic sample prepared from 2a by performing a Birch reduction followed by reduction of the 1,4-diene 12a: (figure presented)
    • The relative stereochemistry of 5a was assigned by comparaison with an authentic sample prepared from 2a by performing a Birch reduction followed by reduction of the 1,4-diene 12a: (figure presented)
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    • The relative stereochemistry of 7a and 7b was assigned by converting them to the corresponding diastereoisomeric carboxylic acids 14a and 14b and comparison with the material obtained from 2a by oxidation of the aromatic ring after acetylation: (figure presented)
    • The relative stereochemistry of 7a and 7b was assigned by converting them to the corresponding diastereoisomeric carboxylic acids 14a and 14b and comparison with the material obtained from 2a by oxidation of the aromatic ring after acetylation: (figure presented)
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    • The relative stereochemistry of 9a and 9b was deduced from the results observed with 4 and 6, and was further confirmed by synthetic transformations of the products (unpublished results)
    • The relative stereochemistry of 9a and 9b was deduced from the results observed with 4 and 6, and was further confirmed by synthetic transformations of the products (unpublished results).
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    • The relative stereochemistry of 11a and 11b was assigned by comparaison with authentic samples respectively prepared from 2a and 2b using the following sequence: (figure presented)
    • The relative stereochemistry of 11a and 11b was assigned by comparaison with authentic samples respectively prepared from 2a and 2b using the following sequence: (figure presented)
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    • The relative stereochemistry of 26a and 26b was established by the following chemical correlation: (figure presented)
    • The relative stereochemistry of 26a and 26b was established by the following chemical correlation: (figure presented)


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