The stereochemistry of solvolysis of an acyclic allylic epoxide

DOI: 10.1016/0957-4166(94)00339-D

Source and publish data:

Tetrahedron Asymmetry p. 15 - 16 (1995)

Update date:2022-08-11

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Boaz

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Article abstract of DOI:10.1016/0957-4166(94)00339-D

In contrast to solvolysis of cyclic allylic epoxides, the acid-catalyzed solvolyses of optically pure 1,2-epoxy-3-butene using water or alcohols show a high degree of inversion stereoselectivity.

Full text of DOI:10.1016/0957-4166(94)00339-D

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Article Doi

The stereochemistry of solvolysis of an acyclic allylic epoxide

DOI: 10.1016/0957-4166(94)00339-D

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0957-4166(94)00339-D

Full text of DOI:10.1016/0957-4166(94)00339-D

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