163705-84-8

Basic information

• Product Name: (1S,2R,αR)-2--1-(carbobenzyloxy)cyclopentane
• Synonyms: (1S,2R,αR)-2--1-(carbobenzyloxy)cyclopentane
• CAS NO: 163705-84-8
• Molecular Weight: 323.435
• Mol File: 163705-84-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1S,2R,αR)-2--1-(carbobenzyloxy)cyclopentane(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R,αR)-2--1-(carbobenzyloxy)cyclopentane(163705-84-8)
• EPA Substance Registry System: (1S,2R,αR)-2--1-(carbobenzyloxy)cyclopentane(163705-84-8)

Safety Data

• Hazardous Substances Data: 163705-84-8(Hazardous Substances Data)

Upstream product

• 163705-82-6 2--amino-1-carbobenzoxycyclopentene 

Downstream Products

• 64191-14-6 cis-2-amino-1-cyclopentane-carboxylic acid 

Relevant articles and documents

An improved synthesis of enantiopure β-amino acids

An improved method for the preparation of both the enantiopure β-amino acids is presented. The diastereomer benzyl β-amino esters, obtained by stereoselective reduction of β-enamino esters, were separated and hydrogenolyzed to the free enantiopure β-amino acids.

Diastereo and Enantioselective Entry to β-Amino Esters by Hydride Reduction of Homochiral β-Enamino Esters.

The reduction of homochiral β-enamino esters 1 with sodium triacetoxyborohydride, which occurs with good diastereo- and enantioselectivity in the β-amino esters 2, is described.The procedure allows a straightforward preparation of compounds with known bio