Enantioselective total syntheses of (-)-allo-coronamic acid, (-)-(Z)-2,3-methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe

José M. Jiménez; Joan Rifé; Rosa M. Ortuño

doi:10.1016/0957-4166(95)00234-G

Enantioselective total syntheses of (-)-allo-coronamic acid, (-)-(Z)-2,3-methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe

José M. Jiménez, Joan Rifé, Rosa M. Ortuño

Department of Chemistry

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

18 Citations (Scopus)

Abstract

The title amino acids have been synthesized in 45, 47, and 63% overall yields, respectively, from enantiopure aminopentenoates, easily available from D-glyceraldehyde as a source of chirality, following divergent pathways from similar diols as common key intermediate compounds. © 1995.

Original language	English
Pages (from-to)	1849-1852
Journal	Tetrahedron: asymmetry
Volume	6
Issue number	8
DOIs	https://doi.org/10.1016/0957-4166(95)00234-G
Publication status	Published - 1 Jan 1995

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title = "Enantioselective total syntheses of (-)-allo-coronamic acid, (-)-(Z)-2,3-methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe",

abstract = "The title amino acids have been synthesized in 45, 47, and 63% overall yields, respectively, from enantiopure aminopentenoates, easily available from D-glyceraldehyde as a source of chirality, following divergent pathways from similar diols as common key intermediate compounds. {\textcopyright} 1995.",

author = "Jim{\'e}nez, {Jos{\'e} M.} and Joan Rif{\'e} and Ortu{\~n}o, {Rosa M.}",

year = "1995",

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T1 - Enantioselective total syntheses of (-)-allo-coronamic acid, (-)-(Z)-2,3-methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe

AU - Jiménez, José M.

AU - Rifé, Joan

AU - Ortuño, Rosa M.

PY - 1995/1/1

Y1 - 1995/1/1

N2 - The title amino acids have been synthesized in 45, 47, and 63% overall yields, respectively, from enantiopure aminopentenoates, easily available from D-glyceraldehyde as a source of chirality, following divergent pathways from similar diols as common key intermediate compounds. © 1995.

AB - The title amino acids have been synthesized in 45, 47, and 63% overall yields, respectively, from enantiopure aminopentenoates, easily available from D-glyceraldehyde as a source of chirality, following divergent pathways from similar diols as common key intermediate compounds. © 1995.

U2 - 10.1016/0957-4166(95)00234-G

DO - 10.1016/0957-4166(95)00234-G

M3 - Article

VL - 6

SP - 1849

EP - 1852

IS - 8

ER -

Enantioselective total syntheses of (-)-allo-coronamic acid, (-)-(Z)-2,3-methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe

Abstract

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