Literature DB >> 22499216

Chiral guanidine-catalyzed asymmetric direct vinylogous Michael reaction of α,β-unsaturated γ-butyrolactams with alkylidene malonates.

Yang Yang1, Shunxi Dong, Xiaohua Liu, Lili Lin, Xiaoming Feng.   

Abstract

The asymmetric direct vinylogous Michael reaction of α,β-unsaturated γ-butyrolactams with alkylidene malonates has been developed. Various 5-substituted 3-pyrrolidin-2-ones were obtained in high yields (up to 93%) with excellent stereoselectivities (up to 94% ee, 95 : 5 dr), using a novel bifunctional C(1)-symmetric guanidine organocatalyst embodied a secondary amine subunit.

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Year:  2012        PMID: 22499216     DOI: 10.1039/c2cc31470c

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


  3 in total

1.  Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions.

Authors:  Alejandro Cabanillas; Christopher D Davies; Louise Male; Nigel S Simpkins
Journal:  Chem Sci       Date:  2014-11-28       Impact factor: 9.825

2.  Bifunctional Iminophosphorane-Catalyzed Enantioselective Sulfa-Michael Addition to Unactivated α,β-Unsaturated Amides.

Authors:  Daniel Rozsar; Michele Formica; Ken Yamazaki; Trevor A Hamlin; Darren J Dixon
Journal:  J Am Chem Soc       Date:  2022-01-06       Impact factor: 15.419

3.  Direct β-selectivity of α,β-unsaturated γ-butyrolactam for asymmetric conjugate additions in an organocatalytic manner.

Authors:  Yuan Zhong; Sihua Hong; Zhengjun Cai; Shixiong Ma; Xianxing Jiang
Journal:  RSC Adv       Date:  2018-08-14       Impact factor: 4.036

  3 in total

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