Manipulation of Substrate-Controlled Diastereoselectivities in Hydroborations in Acyclic Allylamine Derivatives

DOI: 10.1021/jo00003a024

Source and publish data:

Journal of Organic Chemistry p. 1027 - 1036 (1991)

Update date:2022-08-03

Topics:

Authors:

Burgess, Kevin

Ohlmeyer, Michael J.

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Article abstract of DOI:10.1021/jo00003a024

Racemic, and optically active, 2-methyl-3-(N-tosylamino)alkenes I were prepared and subjected to both catalyzed and uncatalyzed hydroborations.Data obtained for the catalyzed hydroborations of these allylamine derivatives are consistent with the theory of

Full text of DOI:10.1021/jo00003a024

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