Directed regiochemical control in the ring expansion reactions of a substituted trans-decalone

DOI: 10.1016/S0040-4039(00)88999-6

Source and publish data:

Tetrahedron Letters p. 2963 - 2966 (1990)

Update date:2022-07-29

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Authors:

Aube, Jeffrey

Hammond, Marlys

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Article abstract of DOI:10.1016/S0040-4039(00)88999-6

A derivative of the Wieland-Miescher ketone can selectively be converted into either regioisomeric ring-expanded lactam. The synthesis of the diastereomeric N-α-methylbenzyl oxaziridine derivatives determines the regiochemistry of the product lactam and a

Full text of DOI:10.1016/S0040-4039(00)88999-6

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