Literature DB >> 11101444

Memory of chirality in diastereoselective alpha-alkylation of isoleucine and allo-isoleucine derivatives.

T Kawabata1, J Chen, H Suzuki, Y Nagae, T Kinoshita, S Chancharunee, K Fuji.   

Abstract

[reaction: see text] alpha-Methylation of 3 gave 5 as a major product whereas 4 gave 6 predominantly, although both 3 and 4 have an (S)-chiral center at C(3). This indicates that chirality at C(2) in 3 and 4 was memorized in the corresponding intermediate enolates and the induced chirality made a major contribution in the stereochemical course of the reaction, while chirality at the adjacent chiral center C(3) had little effect.

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Year:  2000        PMID: 11101444     DOI: 10.1021/ol0066274

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


  4 in total

Review 1.  The Fascinating Chemistry of α-Haloamides.

Authors:  Anna Fantinati; Vinicio Zanirato; Paolo Marchetti; Claudio Trapella
Journal:  ChemistryOpen       Date:  2020-01-13       Impact factor: 2.911

2.  Recent Progress on the Stereoselective Synthesis of Cyclic Quaternary alpha-Amino Acids.

Authors:  Carlos Cativiela; Mario Ordóñez
Journal:  Tetrahedron Asymmetry       Date:  2009-01-30

3.  Radical reactions with double memory of chirality (2MOC) for the enantiospecific synthesis of adjacent stereogenic quaternary centers in solution: cleavage and bonding faster than radical rotation.

Authors:  Marino J E Resendiz; Farnosh Family; Kerrian Fuller; Luis M Campos; Saeed I Khan; Natalia V Lebedeva; Malcolm D E Forbes; Miguel A Garcia-Garibay
Journal:  J Am Chem Soc       Date:  2009-06-24       Impact factor: 15.419

4.  Double nucleophilic addition to iminomalonate, leading to the synthesis of quaternary α-amino diesters and desymmetrization of the products.

Authors:  Makoto Shimizu; Miki Mushika; Isao Mizota; Yusong Zhu
Journal:  RSC Adv       Date:  2019-07-29       Impact factor: 4.036

  4 in total

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