916588-48-2

Upstream product

• 660391-17-3 (2S,5S)-(5-benzyloxymethyl-2,5-dihydro-1H-pyrrol-2-yl)-methanol 
• 660390-94-3 [4S,3(1S)]-3-(1-hydroxymethyl-allyl)-4-vinyl-oxazolidin-2-one 
• 660390-99-8 (3S,6aS)-1,2-dehydro-3-benzyloxymethyl-5-oxapyrrolizidin-4-one 
• 660391-09-3 [4S,3(1S)]-3-[1-benzyloxymethyl-allyl]-4-vinyl-oxazolidin-2-one 
• 660391-00-4 (2S,5S)-2-benzyloxymethyl-5-hydroxymethyl-2,5-dihydro-pyrrole-1-carboxylic acid benzyl ester 
• 660391-10-6 (2S,5S)-5-benzyloxymethyl-2,5-dihydro-pyrrole-1,2-dicarboxylic acid 1-benzyl ester 
• 660391-11-7 (2S,5S)-2-benzyloxymethyl-5-[5-{(5R,7R)-1,6-dioxa-spiro[4.5]dec-7-yl}-pentanoyl]-2,5-dihydro-pyrrole-1-carboxylic acid benzyl ester 
• 660391-02-6 (2S,5S)-5-benzyloxymethyl-5-(methoxy-methyl-carbamoyl)-2,5-dihydro-pyrrole-1-carboxylic acid benzyl ester 

Downstream Products

• 914649-69-7 (2R,3R,4R,5R)-2-benzyloxymethyl-5-[(1S)-5-{(5R,7R)-1,6-dioxa-spiro[4.5]dec-7-yl}-1-hydroxy-pentyl]-3,4-dihydroxy-pyrrolidine-1-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

Palladium-Catalyzed DYKAT of Vinyl Epoxides: Enantioselective Total Synthesis and Assignment of the Configuration of (+)-Broussonetine G

A potential general approach to potent N-heterocyclic glycosidase inhibitors is illustrated by the first total synthesis of (+)-broussonetine G (1). The key transformation of the synthesis relies on two successive palladium-catalyzed asymmetric allylic al