These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Total synthesis of the proposed structure for spirofungin B: a reassignment of the stereochemistry. Author: Zanatta SD, White JM, Rizzacasa MA. Journal: Org Lett; 2004 Mar 18; 6(6):1041-4. PubMed ID: 15012095. Abstract: [structure: see text] The total synthesis of the proposed structure for spirofungin B (2) is described. The data for the synthetic material did not compare with that for the natural product leading to the conclusion that the structure 2 assigned for spirofungin B is incorrect. Analysis of the NMR data reported for spirofungins A and B as well as related spiroketals allowed for the reassignment of the stereochemistry of spirofungin B to be that corresponding to 15-epi-spirofungin A (27).[Abstract] [Full Text] [Related] [New Search]