Literature DB >> 12534300

Alpha-imino esters: versatile substrates for the catalytic, asymmetric synthesis of alpha- and beta-amino acids and beta-lactams.

Andrew E Taggi1, Ahmed M Hafez, Thomas Lectka.   

Abstract

The catalytic asymmetric addition of organic nucleophiles to alpha-imino esters has emerged as one of the most promising and intensely investigated routes to optically enriched alpha- and beta-amino acid derivatives and beta-lactams. The importance of alpha-imino esters stems not only from the vast appeal of the potential product classes,(1) but also from their remarkable reactivity as highly electrophilic imines. With each passing year, the number of publications concerning the asymmetric alkylation of imino esters grows significantly. The asymmetric alkylation of imines(2) and N,O-acetals has been in itself a subject of intense interest.(3) In this Account, we wish to illustrate our contribution to this timely field, as well as to highlight the seminal contributions of others.

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Year:  2003        PMID: 12534300     DOI: 10.1021/ar020137p

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  17 in total

1.  Catalytic, asymmetric reactions of ketenes and ketene enolates.

Authors:  Daniel H Paull; Anthony Weatherwax; Thomas Lectka
Journal:  Tetrahedron       Date:  2009-08-22       Impact factor: 2.457

2.  Enantioselective TADMAP-catalyzed carboxyl migration reactions for the synthesis of stereogenic quaternary carbon.

Authors:  Scott A Shaw; Pedro Aleman; Justin Christy; Jeff W Kampf; Porino Va; Edwin Vedejs
Journal:  J Am Chem Soc       Date:  2006-01-25       Impact factor: 15.419

3.  Hydrogen-mediated reductive coupling of conjugated alkynes with ethyl (N-Sulfinyl)iminoacetates: synthesis of unnatural alpha-amino acids via rhodium-catalyzed C-C bond forming hydrogenation.

Authors:  Jong-Rock Kong; Chang-Woo Cho; Michael J Krische
Journal:  J Am Chem Soc       Date:  2005-08-17       Impact factor: 15.419

4.  Catalytic asymmetric addition of dialkylzinc reagents to alpha-aldiminoesters.

Authors:  Sandeep Basra; Michael W Fennie; Marisa C Kozlowski
Journal:  Org Lett       Date:  2006-06-22       Impact factor: 6.005

5.  Highly enantioselective Mannich reactions with α-aryl silyl ketene acetals and imines.

Authors:  Gregory T Notte; Jenny M Baxter Vu; James L Leighton
Journal:  Org Lett       Date:  2011-01-14       Impact factor: 6.005

6.  Catalytic asymmetric alkynylation of alpha-imino ester: a versatile approach to optically active unnatural alpha-amino acid derivatives.

Authors:  Jian-Xin Ji; Jing Wu; Albert S C Chan
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-01       Impact factor: 11.205

7.  A highly stereoselective synthesis of chiral alpha-amino-beta-lactams via the Kinugasa reaction employing ynamides.

Authors:  Xuejun Zhang; Richard P Hsung; Hongyan Li; Yu Zhang; Whitney L Johnson; Ruth Figueroa
Journal:  Org Lett       Date:  2008-07-10       Impact factor: 6.005

8.  Air-stable, storable, and highly efficient chiral zirconium catalysts for enantioselective Mannich-type, aza Diels-Alder, aldol, and hetero Diels-Alder reactions.

Authors:  Shu Kobayashi; Masaharu Ueno; Susumu Saito; Yumiko Mizuki; Haruro Ishitani; Yasuhiro Yamashita
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-05       Impact factor: 11.205

9.  Asymmetric organocatalytic decarboxylative Mannich reaction using β-keto acids: A new protocol for the synthesis of chiral β-amino ketones.

Authors:  Chunhui Jiang; Fangrui Zhong; Yixin Lu
Journal:  Beilstein J Org Chem       Date:  2012-08-13       Impact factor: 2.883

10.  Construction of chiral α-tert-amine scaffolds via amine-catalyzed asymmetric Mannich reactions of alkyl-substituted ketimines.

Authors:  Chihiro Homma; Aika Takeshima; Taichi Kano; Keiji Maruoka
Journal:  Chem Sci       Date:  2020-11-27       Impact factor: 9.825

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