A Stereoselective Synthesis of Five‐ and Six‐Membered Cyclic β‐Amino Acids | Zendy

Perlmutter Patrick | Zendy; Rose Mark | Zendy; Vounatsos Filisaty | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

A Stereoselective Synthesis of Five‐ and Six‐Membered Cyclic β‐Amino Acids

Author(s) -

Perlmutter Patrick,

Rose Mark,

Vounatsos Filisaty

Publication year - 2003

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200390118

Subject(s) - chemistry , stereoselectivity , imine , ring closing metathesis , metathesis , salt metathesis reaction , stereochemistry , thioester , total synthesis , amino acid , enantioselective synthesis , organic chemistry , catalysis , polymerization , biochemistry , polymer , enzyme

The cyclic β‐amino acids 1 and 2 have been prepared in a short and stereoselective manner. The synthesis features a diastereoselective thioester enolate/imine condensation reaction and a ring‐closing metathesis as key processes. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research