Literature DB >> 21479289

Lithium acetylides as alkynylating reagents for the enantioselective alkynylation of ketones catalyzed by lithium binaphtholate.

Kana Tanaka1, Kenji Kukita, Tomonori Ichibakase, Shunsuke Kotani, Makoto Nakajima.   

Abstract

Chiral lithium binaphtholate effectively catalyzed the enantioselective alkynylation of ketones using lithium acetylide as an alkynylating agent. This is the first example of the catalytic enantioselective addition of lithium acetylide to carbonyl compounds without the aid of other metal sources. © The Royal Society of Chemistry 2011

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21479289     DOI: 10.1039/c1cc10734h

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


  2 in total

1.  Merging Asymmetric [1,2]-Additions of Lithium Acetylides to Carbonyls with Type II Anion Relay Chemistry.

Authors:  Kevin T O'Brien; Amos B Smith
Journal:  Org Lett       Date:  2019-09-09       Impact factor: 6.005

2.  Enantioselective Evans-Tishchenko reduction of β-hydroxyketone catalyzed by lithium binaphtholate.

Authors:  Tomonori Ichibakase; Masato Nakatsu; Makoto Nakajima
Journal:  Molecules       Date:  2011-06-17       Impact factor: 4.411

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.