284482-56-0

Basic information

• Product Name: (3R,5R)-3-Benzoyloxymethyl-5-((E)-2-methoxy-vinyl)-piperidine-1-carboxylic acid benzyl ester
• Synonyms: (3R,5R)-3-Benzoyloxymethyl-5-((E)-2-methoxy-vinyl)-piperidine-1-carboxylic acid benzyl ester
• CAS NO: 284482-56-0
• Molecular Weight: 409.482
• Mol File: 284482-56-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,5R)-3-Benzoyloxymethyl-5-((E)-2-methoxy-vinyl)-piperidine-1-carboxylic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,5R)-3-Benzoyloxymethyl-5-((E)-2-methoxy-vinyl)-piperidine-1-carboxylic acid benzyl ester(284482-56-0)
• EPA Substance Registry System: (3R,5R)-3-Benzoyloxymethyl-5-((E)-2-methoxy-vinyl)-piperidine-1-carboxylic acid benzyl ester(284482-56-0)

Safety Data

• Hazardous Substances Data: 284482-56-0(Hazardous Substances Data)

Upstream product

• 613-90-1 benzoyl cyanide 

Downstream Products

• 284482-57-1 (3R,5R)-3-Benzoyloxymethyl-5-(1,3,4,9-tetrahydro-pyrano[3,4-b]indol-1-ylmethyl)-piperidine-1-carboxylic acid benzyl ester 
• 284482-59-3 (3R,5S)-3-Benzoyloxymethyl-5-{2-[3-(2-methanesulfonyloxy-ethyl)-1H-indol-2-yl]-ethyl}-piperidine-1-carboxylic acid benzyl ester 
• 284482-58-2 (3R,5S)-3-Benzoyloxymethyl-5-{2-[3-(2-hydroxy-ethyl)-1H-indol-2-yl]-ethyl}-piperidine-1-carboxylic acid benzyl ester 

Relevant articles and documents

Indole alkaloids by a chemoenzymatic approach: Two convergent routes for the first enantioselective synthesis of (+)-20R-15,20-dihydrocleavamine

A stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. Two alternative strategies have been developed to ensure the critical formation of the nine-membered ring of 3. (C) 2000 Elsevier Science Ltd.