STEREOSELECTIVITY IN INTRAMOLECULAR 1,3-DIPOLAR CYCLOADDITIONS. NITRILE OXIDES VERSUS SILYL NITRONATES

DOI: 10.1016/S0040-4039(00)94618-5

Source and publish data:

Tetrahedron Letters p. 743 - 746 (1990)

Update date:2022-07-30

Topics:

Authors:

Dehaen, W.

Hassner, A.

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Article abstract of DOI:10.1016/S0040-4039(00)94618-5

Unlike nitrile oxides, silyl nitronates undergo highly stereoselective intramolecular cycloadditions to produce functionalized carbocyclic or heterocyclic rings.

Full text of DOI:10.1016/S0040-4039(00)94618-5

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