Enantiospecific synthesis of 3-pyrrolines: A route to novel polyhydroxylated pyrrolidines

DOI: 10.1016/0040-4039(94)88236-3

Source and publish data:

Tetrahedron Letters p. 7099 - 7102 (1994)

Update date:2022-08-03

Topics: Novel Route 3-pyrrolines Enantiospecific synthesis

Authors:

Burley, Ian

Hewson, Alan T.

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Article abstract of DOI:10.1016/0040-4039(94)88236-3

Enantiomer acetamido ketones are converted by an intramolecular Wittig reaction into enantiopure 3-pyrrolines; the product from (S)-serine provides access to novel polyhydroxylated pyrrolidines.

Full text of DOI:10.1016/0040-4039(94)88236-3

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