STEREOSELECTIVITY IN CYCLOADDITION OF PHENYLGLYOXYLNITRILE OXIDE TO 7-SUBSTITUTED NORBORNADIENES AND 8-SUBSTITUTED 2-AZABICYCLOOCT-3,6-DIENES

DOI: 10.1016/0040-4039(81)80044-5

Source and publish data:

Tetrahedron Letters p. 73 - 76 (1981)

Update date:2022-08-05

Topics:

Authors:

Umano, Katsumi

Mizone, Shinya

Tokisato, Kazuhiko

Inoue, Hiroo

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Article abstract of DOI:10.1016/0040-4039(81)80044-5

The cycloaddition of phenylglyoxylonitrile oxide to the 7-substituted norbornadienes 1a-c gives predominantly the endo isomers, but that to the 8-substituted 2-azabicyclo<3.2.1>oct-3,6-dienes 2a-b the exo isomers.

Full text of DOI:10.1016/0040-4039(81)80044-5

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