ETUDE DE LA DIASTEREOSELECTIVITE DE LA CYCLOADDITION DIPOLAIRE-1,3 REACTION DES AZIDES SUR LES METHOXYCARBONYL-3 DIHYDRO-1,2 NAPHTALENES SUBSTITUES ET QUELQUES COMPOSES APPARENTES

DOI: 10.1016/S0040-4020(01)88636-1

Source and publish data:

Tetrahedron p. 4163 - 4174 (1983)

Update date:2022-08-05

Topics:

Authors:

Vebrel, Joel

Carrie, Robert

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Article abstract of DOI:10.1016/S0040-4020(01)88636-1

Cycloaddition of azides to 1-or 2-monosubstituted 3-methoxycarbonyl-1,2-dihydro naphtalenes is diastereospecific.The determinant effect revealing a dominant role of conformational factors on the stereochemistry of these reactions.

Full text of DOI:10.1016/S0040-4020(01)88636-1

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Product name:Indeno[1,2-d]triazole-3a(1H)-carboxylic acid, 8,8a-dihydro-1-phenyl-, methyl ester, cis-

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