The hydrocyanation route to β- and γ-amino acids. A synthesis of α-methylene-β-alanine

W. Roy Jackson; Patrick Perlmutter; Andrew J. Smallridge

doi:10.1016/S0040-4039(00)82095-X

The hydrocyanation route to β- and γ-amino acids. A synthesis of α-methylene-β-alanine

W. Roy Jackson, Patrick Perlmutter, Andrew J. Smallridge

School of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

14 Citations (Scopus)

Abstract

Hydrocyanation of several phthalimidoalkynes proceeds with good regioselection yielding products which were easily converted into unsaturated and saturated β- and γ-amino acids.

Original language	English
Pages (from-to)	1983-1984
Number of pages	2
Journal	Tetrahedron Letters
Volume	29
Issue number	16
DOIs	https://doi.org/10.1016/S0040-4039(00)82095-X
Publication status	Published - 1 Jan 1988

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10.1016/S0040-4039(00)82095-X

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Cite this

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title = "The hydrocyanation route to β- and γ-amino acids. A synthesis of α-methylene-β-alanine",

abstract = "Hydrocyanation of several phthalimidoalkynes proceeds with good regioselection yielding products which were easily converted into unsaturated and saturated β- and γ-amino acids.",

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AU - Perlmutter, Patrick

AU - Smallridge, Andrew J.

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Y1 - 1988/1/1

N2 - Hydrocyanation of several phthalimidoalkynes proceeds with good regioselection yielding products which were easily converted into unsaturated and saturated β- and γ-amino acids.

AB - Hydrocyanation of several phthalimidoalkynes proceeds with good regioselection yielding products which were easily converted into unsaturated and saturated β- and γ-amino acids.

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U2 - 10.1016/S0040-4039(00)82095-X

DO - 10.1016/S0040-4039(00)82095-X

M3 - Article

AN - SCOPUS:0005142230

VL - 29

SP - 1983

EP - 1984

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

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