Literature DB >> 26704528

Asymmetric Direct 1,2-Addition of Aryl Grignard Reagents to Aryl Alkyl Ketones.

Kazuki Osakama1, Makoto Nakajima1.   

Abstract

The enantioselective addition of Grignard reagents to ketones was promoted by a BINOL derivative bearing alkyl chains at the 3,3'-positions. This is the first asymmetric direct aryl Grignard addition to ketones reported to date. A variety of tertiary diaryl alcohols could be obtained in high yields and enantioselectivities without using any other metal source.

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Year:  2015        PMID: 26704528     DOI: 10.1021/acs.orglett.5b03379

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

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Authors:  Yuyang Dong; Alexander W Schuppe; Binh Khanh Mai; Peng Liu; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2022-03-26       Impact factor: 16.383

2.  Asymmetric addition of Grignard reagents to ketones: culmination of the ligand-mediated methodology allows modular construction of chiral tertiary alcohols.

Authors:  Claudio Monasterolo; Ryan O'Gara; Saranna E Kavanagh; Sadbh E Byrne; Bartosz Bieszczad; Orla Murray; Michael Wiesinger; Rebecca A Lynch; Kirill Nikitin; Declan G Gilheany
Journal:  Chem Sci       Date:  2022-04-20       Impact factor: 9.969

3.  Enantioselective para-Claisen Rearrangement for the Synthesis of Illicium-Derived Prenylated Phenylpropanoids.

Authors:  Joshua A Homer; Irene De Silvestro; Eilidh J Matheson; Jake T Stuart; Andrew L Lawrence
Journal:  Org Lett       Date:  2021-04-15       Impact factor: 6.005

  3 in total

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