PYRROLIDINE RING FORMATION BY A NEW BASE-PROMOTED 1,3-DIPOLAR CYCLOADDITION OF N-(PHENYLTHIOMETHYL)AMINO ACID ESTERS

DOI: 10.1016/S0040-4039(01)90015-2

Source and publish data:

Tetrahedron Letters p. 1579 - 1582 (1984)

Update date:2022-07-30

Topics:

Authors:

Imai, Nobuyuki

Terao, Yoshiyasu

Achiwa, Kazuo

Sekiya, Minoru

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Article abstract of DOI:10.1016/S0040-4039(01)90015-2

N-Phenylthiomethyl derivatives of α-amino acid esters are attacked by α,β-unsaturated carboxylates in the presence of sodium hydride, undergoing 1,3-dipolar cycloaddition to give pyrrolidines.

Full text of DOI:10.1016/S0040-4039(01)90015-2

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