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

Isao Shimizu, Tomoko Ishikawa

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

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

Original languageEnglish
Pages (from-to)1905-1908
Number of pages4
JournalTetrahedron Letters
Volume35
Issue number12
DOIs
Publication statusPublished - 1994 Mar 21

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formic acid
Palladium
isoclavukerin
clavukerin A

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid. / Shimizu, Isao; Ishikawa, Tomoko.

In: Tetrahedron Letters, Vol. 35, No. 12, 21.03.1994, p. 1905-1908.

Research output: Contribution to journalArticle

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