Organic Letters, volume 14, issue 7, pages 1661-1663

Total Synthesis of the Terpenoid Buddledone A: 11-Membered Ring-Closing Metathesis

Zhengxin Cai ¹

Nattawut Yongpruksa ¹

M. Harmata ¹

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Department of Chemistry, University of Missouri—Columbia, Columbia, Missouri 65211, United States |

Publication type: Journal Article

Publication date: 2012-03-20

American Chemical Society (ACS)

Journal: Organic Letters

scimago Q1

SJR: 1.245

CiteScore: 9.3

Impact factor: 4.9

ISSN: 15237060, 15237052

DOI: 10.1021/ol300400x

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PubMed ID: 22432972

Organic Chemistry

Biochemistry

Physical and Theoretical Chemistry

Abstract

The first total synthesis of buddledone A was accomplished in seven steps from methyl ethyl ketone (MEK). The key step in the sequence featured an 11-membered ring formation by ring-closing metathesis.

Found

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Publisher

American Chemical Society (ACS)

Journal

Organic Letters

scimago Q1

SJR

1.245

CiteScore

9.3

Impact factor

4.9

ISSN

15237060 (Print)

15237052 (Electronic)

Total Synthesis of the Terpenoid Buddledone A: 11-Membered Ring-Closing Metathesis

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