Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid

Isao Shimizu; Tomoko Ishikawa

doi:10.1016/S0040-4039(00)73192-3

Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid

Isao Shimizu^*, Tomoko Ishikawa

^*Corresponding author for this work

Waseda University

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

12 Citations (Scopus)

Abstract

(±)-Clavukerin A and (±)-isoclavukerin A were synthesized stereoselectively utilizing stereospecific palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid.

Original language	English
Pages (from-to)	1905-1908
Number of pages	4
Journal	Tetrahedron Letters
Volume	35
Issue number	12
DOIs	https://doi.org/10.1016/S0040-4039(00)73192-3
Publication status	Published - 1994 Mar 21

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

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10.1016/S0040-4039(00)73192-3

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title = "Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid",

abstract = "(±)-Clavukerin A and (±)-isoclavukerin A were synthesized stereoselectively utilizing stereospecific palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid.",

author = "Isao Shimizu and Tomoko Ishikawa",

year = "1994",

month = mar,

day = "21",

doi = "10.1016/S0040-4039(00)73192-3",

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pages = "1905--1908",

journal = "Tetrahedron Letters",

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number = "12",

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T1 - Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid

AU - Shimizu, Isao

AU - Ishikawa, Tomoko

PY - 1994/3/21

Y1 - 1994/3/21

N2 - (±)-Clavukerin A and (±)-isoclavukerin A were synthesized stereoselectively utilizing stereospecific palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid.

AB - (±)-Clavukerin A and (±)-isoclavukerin A were synthesized stereoselectively utilizing stereospecific palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid.

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U2 - 10.1016/S0040-4039(00)73192-3

DO - 10.1016/S0040-4039(00)73192-3

M3 - Article

AN - SCOPUS:0028288682

SN - 0040-4039

VL - 35

SP - 1905

EP - 1908

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 12

ER -

Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid

Abstract

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