The stereoselective construction of E- and Z-Δ-Ile from E-dehydroamino acid ester: the synthesis of the phomopsin A tripeptide side chain

Yoko Yasuno; Akito Nishimura; Yoshifumi Yasukawa; Yuma Karita; Yasufumi Ohfune; Tetsuro Shinada

doi:10.1039/c5cc08458j

The stereoselective construction of E- and Z-Δ-Ile from E-dehydroamino acid ester: the synthesis of the phomopsin A tripeptide side chain

Yoko Yasuno
, Akito Nishimura
, Yoshifumi Yasukawa
, Yuma Karita
, Yasufumi Ohfune
, Tetsuro Shinada

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

11 Citations (Scopus)

Abstract

The stereoselective synthesis of the phomopsin A tripeptide side chain was achieved by using methyl 2-(((benzyloxy)carbonyl)amino)-2-(diphenoxyphosphoryl)acetate as a common synthetic precursor for the synthesis of E-Δ-dehydroisoleucine and E-Δ-aspartate.

Original language	English
Pages (from-to)	1478-1481
Number of pages	4
Journal	Chemical Communications
Volume	52
Issue number	7
DOIs	https://doi.org/10.1039/c5cc08458j
Publication status	Published - Jan 25 2016
Externally published	Yes

All Science Journal Classification (ASJC) codes

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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10.1039/c5cc08458j

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abstract = "The stereoselective synthesis of the phomopsin A tripeptide side chain was achieved by using methyl 2-(((benzyloxy)carbonyl)amino)-2-(diphenoxyphosphoryl)acetate as a common synthetic precursor for the synthesis of E-Δ-dehydroisoleucine and E-Δ-aspartate.",

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T2 - the synthesis of the phomopsin A tripeptide side chain

AU - Yasuno, Yoko

AU - Nishimura, Akito

AU - Yasukawa, Yoshifumi

AU - Karita, Yuma

AU - Ohfune, Yasufumi

AU - Shinada, Tetsuro

N1 - Publisher Copyright: © The Royal Society of Chemistry.

PY - 2016/1/25

Y1 - 2016/1/25

N2 - The stereoselective synthesis of the phomopsin A tripeptide side chain was achieved by using methyl 2-(((benzyloxy)carbonyl)amino)-2-(diphenoxyphosphoryl)acetate as a common synthetic precursor for the synthesis of E-Δ-dehydroisoleucine and E-Δ-aspartate.

AB - The stereoselective synthesis of the phomopsin A tripeptide side chain was achieved by using methyl 2-(((benzyloxy)carbonyl)amino)-2-(diphenoxyphosphoryl)acetate as a common synthetic precursor for the synthesis of E-Δ-dehydroisoleucine and E-Δ-aspartate.

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UR - https://www.scopus.com/pages/publications/84954436779#tab=citedBy

U2 - 10.1039/c5cc08458j

DO - 10.1039/c5cc08458j

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ER -

The stereoselective construction of E- and Z-Δ-Ile from E-dehydroamino acid ester: the synthesis of the phomopsin A tripeptide side chain

Abstract

All Science Journal Classification (ASJC) codes

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