Stereoselective synthesis of a dialkylhydantoin featuring an asymmetric Strecker reaction on an acyclic dialkyl ketone

Gill, Duncan M. (2012) Stereoselective synthesis of a dialkylhydantoin featuring an asymmetric Strecker reaction on an acyclic dialkyl ketone. Tetrahedron Letters, 53 (15). pp. 1951-1953. ISSN 0040-4039

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Abstract

A diastereoselective Strecker reaction using (R)-(-)-phenylglycinol forms the basis of a concise scalemic route to dialkylhydantoin 1. The phenylglycinol functionality was exploited in the manipulation of the aminonitrile Strecker product through to the dialkylhydantoin via a short, efficient sequence involving crystalline intermediates.

Information

URI:

https://eprints.hud.ac.uk/id/eprint/13698

Title:

Stereoselective synthesis of a dialkylhydantoin featuring an asymmetric Strecker reaction on an acyclic dialkyl ketone

Creators:

Gill, Duncan M.

Identification Number:

https://doi.org/10.1016/j.tetlet.2012.02.008

Official URL:

http://dx.doi.org/10.1016/j.tetlet.2012.02.008

Date: