890122-49-3Relevant academic research and scientific papers
A stereodivergent strategy to both product enantiomers from the same enantiomer of a stereoinducing catalyst: agelastatin
Trost, Barry M.,Dong, Guangbin
supporting information; experimental part, p. 6910 - 6919 (2010/02/28)
In this article, we report a full account of our recent development of pyrroles and N-alkoxyamides as new classes of nucleophiles for palladiumcatalyzed AAA reactions, along with application of these methodologies in the total synthesis of agelastatin A,
New class of nucleophiles for palladium-catalyzed asymmetric allylic alkylation. Total synthesis of agelastatin A
Trost, Barry M.,Dong, Guangbin
, p. 6054 - 6055 (2007/10/03)
New classes of nucleophiles, pyrroles, and N-methoxyamides were developed for Pd-catalyzed AAA reactions. By varying the functional groups at the 2-position of pyrroles, either regioisomer of the piperazinone is available. Using one regioisomer, the total
