Literature DB >> 30301346

Synthesis of Phenolic Glycosides: Glycosylation of Sugar Lactols with Aryl Bromides via Dual Photoredox/Ni Catalysis.

Hui Ye1,2, Cong Xiao3, Quan-Quan Zhou1, Peng George Wang3, Wen-Jing Xiao1,2.   

Abstract

Multifarious sugar lactols were efficiently transformed into the corresponding phenolic glycosides by treating with aryl bromides in acetonitrile with Ir[dF(CF3)ppy]2(dtbbpy)(PF6) as a photocatalyst under visible light irradiation. Both pyranoses and furanoses or even disaccharide could all suffer this glycosylation protocol under mild reaction conditions. A variety of phenyl glycosides can be produced in moderate to good yields (up to 93% yield), and a gram scale process of this protocol was also well-established.

Entities:  

Year:  2018        PMID: 30301346     DOI: 10.1021/acs.joc.8b02129

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Site-selective redox isomerizations of furanosides using a combined arylboronic acid/photoredox catalyst system.

Authors:  Victoria Dimakos; Daniel Gorelik; Hsin Y Su; Graham E Garrett; Gregory Hughes; Hiromitsu Shibayama; Mark S Taylor
Journal:  Chem Sci       Date:  2020-01-03       Impact factor: 9.825

2.  Ceramic boron carbonitrides for unlocking organic halides with visible light.

Authors:  Tao Yuan; Meifang Zheng; Markus Antonietti; Xinchen Wang
Journal:  Chem Sci       Date:  2021-03-23       Impact factor: 9.825

  2 in total

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