Literature DB >> 25504614

Bifunctional N-heterocyclic carbene catalyzed [3+4] annulation of enals and aurones.

Zhi-Qin Liang1, Zhong-Hua Gao, Wen-Qiang Jia, Song Ye.   

Abstract

Bifunctional N-heterocyclic carbenes with a free hydroxy group are demonstrated as efficient catalysts for the [3+4] annulation of enals with aurones to give the corresponding benzofuran-fused ε-lactones in good yields with good diastereoselectivities and excellent enantioselectivities. Control experiments reveal that the [3+4] cycloadducts are kinetically favored and could be transformed to the thermodynamically favored [3+2] cycloadducts with a non-bifunctional NHC catalyst.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  N-heterocyclic carbenes; annulation; kinetic control; lactones; organocatalysis

Year:  2014        PMID: 25504614     DOI: 10.1002/chem.201405828

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  Mechanism and stereoselectivity in NHC-catalyzed β-functionalization of saturated carboxylic ester.

Authors:  Yan Li; Zhiqiang Zhang
Journal:  RSC Adv       Date:  2019-03-06       Impact factor: 4.036

2.  Enantioselective annulation of enals with 2-naphthols by triazolium salts derived from l-phenylalanine.

Authors:  Guo-Tai Li; Qing Gu; Shu-Li You
Journal:  Chem Sci       Date:  2015-04-30       Impact factor: 9.825

3.  Catalyst-controlled regioselectivity in phosphine catalysis: the synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate.

Authors:  Huanzhen Ni; Zhaoyuan Yu; Weijun Yao; Yu Lan; Nisar Ullah; Yixin Lu
Journal:  Chem Sci       Date:  2017-06-12       Impact factor: 9.825

  3 in total

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