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. 2013 Jun 5;3(3):117–120. doi: 10.1007/s13659-013-0034-7

Total synthesis of 1-oxomiltirone via Suzuki coupling

Chun-Miao Li 1,3, Hui-Chun Geng 1,2, Ming-Ming Li 1, Gang Xu 1, Tie-Jun Ling 3, Hong-Bo Qin 1,
PMCID: PMC4131665

Abstract

Abietane diterpenes and miltirone series have shown important activities and for medical purposes in order to achieve the total synthesis of 1-oxomiltrone 1 and miltirone 4, a versatile intermediate 6 was found. The compound 6 could be used as a precursor A-B-C rings with different oxidative degrees in selected abietane diterpenes when synthesized through high yield Suzuki reaction and subsequent cyclization, and total synthesis of 1-oxomiltirone (1) has been achieved. graphic file with name 13659_2013_34_Article_Fig1_HTML.jpg

Electronic Supplementary Material

Supplementary material is available for this article at 10.1007/s13659-013-0034-7 and is accessible for authorized users.

Keywords: total synthesis, Suzuki coupling, 1-oxomiltirone, abietane diterpenes, versatile intermediate

Electronic supplementary material

13659_2013_34_MOESM1_ESM.pdf (1.1MB, pdf)

Supplementary material, approximately 1.09 MB.

Footnotes

This article is published with open access at Springerlink.com

Contributor Information

Tie-Jun Ling, Email: lingtj@ahau.edu.cn.

Hong-Bo Qin, Email: qinhongbo@mail.kib.ac.cn.

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Supplementary Materials

13659_2013_34_MOESM1_ESM.pdf (1.1MB, pdf)

Supplementary material, approximately 1.09 MB.


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