Author's Organization:Department of Chemistry of Medicinal Natural Products, School of Pharmacy, West China University of Medical Sciences Department of Chemistry of Medicinal Natural Products, School of Pharmacy, West China University of Medical Sciences Department of Chemistry of Medicinal Natural Products, School of Pharmacy, West China University of Medical Sciences Department of Chemistry of Medicinal Natural Products, School of Pharmacy, West China University of Medical Sciences Chengdu Institute of Biology, Chinese Academy of Sciences
Published: December 01, 2000Received: June 16, 2000Available on J-STAGE: March 31, 2008Accepted: August 16, 2000
Advance online publication: -
Revised: -
New access to the 7, 17-seco norditerpenoid alkaloids 9 (60%) from yunnaconitine (5), as well as 14 (46%) and 15 (22%) from isotalatizidine (10), via selective hydrolysis, chlorination and reduction with NaBH4 is described.