Promotion of water in BPL-catalyzed asymmetric cross aldol reaction-Reference-Cited by-同舟云学术

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Promotion of water in BPL-catalyzed asymmetric cross aldol reaction

Published:2020-04-17 Issue: Volume: Page:
ISSN:2190-6815
Container-title:Biomass Conversion and Biorefinery
language:en
Short-container-title:Biomass Conv. Bioref.

Author:

Wang Yun,Liang Xin-Yi,Chen Xin-Yi,Liang Zhi-Hui,Cheng Hong,Li Xiang,Li Li-Ling

Funder

Natural Science Foundation of Guangdong Province

Special Innovation Projects of Common Universities in Guangdong Province

Publisher

Springer Science and Business Media LLC

Subject

Renewable Energy, Sustainability and the Environment

Link

https://link.springer.com/content/pdf/10.1007/s13399-020-00695-0.pdf

Reference31 articles.

1. Dwivedee BP, Soni S, Sharma M, Bhaumik J, Laha JK, Banerjee UC (2018) Promiscuity of lipase-catalyzed reactions for organic synthesis: a recent update. ChemistrySelect 3(9):2441–2466. https://doi.org/10.1002/slct.201702954

2. He WX, Xing X, Yang ZJ, Yu Y, Wang N, Yu XQ (2019) Biocatalytic one-pot three-component synthesis of indoloquinolizines with high diastereoselectivity. Catal Lett 249(2):638–643. https://doi.org/10.1007/s10562-019-02660-7

3. Koszelewski D, Ostaszewski R (2019) Biocatalytic promiscuity of lipases in carbon-phosphorus bond formation. ChemCatChem 11(10):2554–2558. https://doi.org/10.1002/cctc.201900397

4. Cai JF, Guan Z, He YH (2011) The lipase-catalyzed asymmetric C–C Michael addition. J Mol Catal B Enzym 68(3–4):240–244. https://doi.org/10.1016/j.molcatb.2010.11.011

5. Rizzo PVS, Boarin LA, Freitas IOM, Gomes RS, Beatriz A, Rinaldi AW, Domingues NLC (2014) The study of biocatalyzed thio-Michael reaction: a greener and multi-gram protocol. Tetrahedron Lett 55(2):430–434. https://doi.org/10.1016/j.tetlet.2013.11.047

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3. Caesium carbonate functionalized magnetic nanoparticles: An efficient heterogeneous and reusable inorganic catalyst for aldol reaction in water;Inorganic Chemistry Communications;2023-03

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