REGIOCHEMICAL PREFERENCES IN SELENOALDEHYDE CYCLOADDITIONS

DOI: 10.1016/S0040-4039(00)95607-7

Source and publish data:

Tetrahedron Letters p. 5121 - 5124 (1987)

Update date:2022-08-04

Topics:

Authors:

Meinke, Peter T.

Krafft, Grant A.

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Article abstract of DOI:10.1016/S0040-4039(00)95607-7

The regiochemical preferences of substituted selenoaldehydes in cycloaddition reactions with electronically biased dienes have been examined.Selenoaldehydes substituted with electronwithdrawing groups exhibit "ortho-para" orientation, while selenoaldehyde

Full text of DOI:10.1016/S0040-4039(00)95607-7

Products guided by the article

Product name:tert-Butyl-[(1S,3R,4R)-3-(2,4-dinitro-phenyl)-2-selena-bicyclo[2.2.2]oct-5-en-6-yloxy]-dimethyl-silane

Cas No:114105-44-1

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