501096-29-3

Upstream product

• 193264-89-0 (S)-2-(tert-Butyl-dimethyl-silanyloxymethyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl ester 
• 501096-23-7 (5S)-1-(tert-butoxycarbonyl)-5-hydroxymethyl-2-pyrroline 

Downstream Products

• 501096-31-7 [4-((2S,3S,4R,5R)-3,4-Dihydroxy-5-hydroxymethyl-pyrrolidin-2-yl)-phenyl]-carbamic acid methyl ester 
• 501096-30-6 (1S)-N-(tert-butoxycarbonyl)-1-(p-carbomethoxyamino-phenyl)-1,4-dideoxy-1,4-imino-D-ribitol 

Relevant academic research and scientific papers

Stereoselective synthesis of aza analogues of isoaltholactone and goniothalesdiol - New applications of the Heck-Matsuda reaction

The stereoselective synthesis of nitrogen analogues of biologically active isoaltholactone and goniothalesdiol are described. The successful strategy employed a Heck-Matsuda reaction between a chiral endocyclic enecarbamate bearing an ester functionality

Probing the stereoselectivity of the Heck arylation of endocyclic enecarbamates with diazonium salts. Concise syntheses of (2S,5R)-phenylproline methyl ester and Schramm's C-azanucleoside.

[reaction: see text] The diastereoselectivity of the Heck arylation of several chiral, nonracemic, five-membered endocyclic enecarbamates with aryldiazonium tetrafluoroborates was evaluated. The cis selectivity observed for some enecarbamates bearing coor