Literature DB >> 15543302

Stereoconservative Negishi arylation and alkynylation as an efficient approach to enantiopure 2,2'-diarylated 1,1'-binaphthyls.

Katarína Krascsenicsová1, Peter Walla, Peter Kasák, Georg Uray, C Oliver Kappe, Martin Putala.   

Abstract

Negishi arylation and alkynylation of easily synthesized chiral 2,2'-diodo-1,1'-binaphthyl rapidly proceeds in refluxing THF utilizing controlled microwave irradiation, affording enantiopure 2,2'-diarylated 1,1'-binaphthyls in good to excellent yields.

Entities:  

Year:  2004        PMID: 15543302     DOI: 10.1039/b410185e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

Review 1.  Controlled microwave heating in modern organic synthesis: highlights from the 2004-2008 literature.

Authors:  C Oliver Kappe; Doris Dallinger
Journal:  Mol Divers       Date:  2009-04-21       Impact factor: 2.943

2.  Rapid Synthesis of Boc-2',6'-dimethyl-l-tyrosine and Derivatives and Incorporation into Opioid Peptidomimetics.

Authors:  Aaron M Bender; Nicholas W Griggs; Chao Gao; Tyler J Trask; John R Traynor; Henry I Mosberg
Journal:  ACS Med Chem Lett       Date:  2015-10-19       Impact factor: 4.345

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.