E-mail a Wiley Online Library Link

Haizhen Zhang and Fajun Nan Synthesis toward the Lindenane-type Sesquiterpenoid Monomer of Chlorahololide A Chinese Journal of Chemistry 31

Version of Record online: 11 DEC 2012 | DOI: 10.1002/cjoc.201200695

Thumbnail image of graphical abstract

Starting from alcohol (2), and on the basis of Yamamoto rearrangement, intramolecular cyclopropanation reaction, 1,3-dipolar cyclization, and intramolecular Heck reaction, the Lindenane-type sesquiterpenoid fragement (20) of Chlorahololide A (1) has been synthesized in a linear sequence of 21 steps and an overall yield of 1.8%. The flexible synthetic route could generate further natural products of the Chloranthaceae family.

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field