Noah Burns and co-workers from Stanford have reported in JACS on the syntheses of (−)-deschloromytilipin A and (−)-danicalipin A.
Posted by naturalproductman on April 8, 2016
Noah Burns and co-workers from Stanford have reported in JACS on the syntheses of (−)-deschloromytilipin A and (−)-danicalipin A.
Posted in Chlorosulpholipids, Halogenated, Lipids, Methodology, Total Synthesis | Leave a Comment »
Posted by naturalproductman on February 2, 2016
Peter Northcote and co-workers from the Victoria University of Wellington have reported in the Journal of Natural Products on the isolation of a bromo-, chloro-, iodo- containing natural product.
Posted in Halogenated, Indoles | Leave a Comment »
Posted by naturalproductman on September 30, 2015
Noah Burns and co-workers at Stanford have reported in JACS on some deceptively simple looking molecules.
Posted in Asymmetric, Halogenated, Methodology, Total Synthesis | Leave a Comment »
Posted by naturalproductman on September 25, 2015
Tadeusz Molinski and co-workers have reported in JACS on the isolation and characterization of mollenynes B-E.
JACS paper
Posted in Alkynes, Computational, DFT, Halogenated, New Techniques, NMR, Peptides, Polyenes, Stereochemistry | Leave a Comment »
Posted by naturalproductman on May 13, 2015
Stefan Schulz and co-workers at TU Braunschweig have reported in ACIE on the isolation of a polychlorinated natural product from the snow flea.
There’s a typo in the description of the article: ” in which α-vinylation of a lactone and ring-closing metathesis are they key steps.” should be “are the key steps.”
ACIE paper
Posted in Halogenated | Leave a Comment »