Promiscuity of Lipase-Catalyzed Reactions for Organic Synthesis: A Recent Update-Reference-Cited by-同舟云学术

Promiscuity of Lipase-Catalyzed Reactions for Organic Synthesis: A Recent Update

Published:2018-03-02 Issue:9 Volume:3 Page:2441-2466
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
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Author:

Dwivedee Bharat P.¹,Soni Surbhi²,Sharma Misha³,Bhaumik Jayeeta¹,Laha Joydev K.³,Banerjee Uttam C.¹^ORCID

Affiliation:

1. Department of Pharmaceutical Technology (Biotechnology); National Institute of Pharmaceutical Education and Research; S.A.S. Nagar 160062 Punjab India

2. Department of Biotechnology; National Institute of Pharmaceutical Education and Research, S.A.S. Nagar; 160062 Punjab India

3. Department of Pharmaceutical Technology (Process Chemistry); National Institute of Pharmaceutical Education and Research; S.A.S. Nagar 160062 Punjab India

Funder

DST-INSPIRE fellowship provided by the Department of Science and Technology

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/slct.201702954/fullpdf

Reference133 articles.

1. Hydrolases: catalytically promiscuous enzymes for non-conventional reactions in organic synthesis

2. Recent Advances in Biocatalytic Promiscuity: Hydrolase-Catalyzed Reactions for Nonconventional Transformations

3. Evidence for the Formation of an Enamine Species during Aldol and Michael-type Addition Reactions Promiscuously Catalyzed by 4-Oxalocrotonate Tautomerase

4. The use of lipases as biocatalysts for the epoxidation of fatty acids and phenolic compounds

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