Literature DB >> 29896683

Glycosyl Sulfoxides in Glycosylation Reactions.

Jing Zeng1,2, Yan Liu1,2, Wei Chen1,2, Xiang Zhao1,2, Lingkui Meng1,2, Qian Wan3,4.   

Abstract

Carbohydrate chemistry has benefited a lot from the intrinsic reactivity of sulfoxide since it was introduced in glycosylation reactions by Kahne in 1989. Since then, extensive studies have been explored by employing sulfoxide as glycosyl donors and activation reagents in construction of glycosidic bonds. As glycosyl donors, the sulfinyl groups could locate either directly or remotely at anomeric position. This chapter focuses on the establishment and development of sulfoxides as glycosyl donors in glycosylation reactions, with an emphasis on their applications and postulated mechanisms.

Entities:  

Keywords:  Carbohydrate; Glycosylation; Sulfoxide

Year:  2018        PMID: 29896683     DOI: 10.1007/s41061-018-0205-4

Source DB:  PubMed          Journal:  Top Curr Chem (Cham)        ISSN: 2364-8961


  3 in total

1.  Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts.

Authors:  Daniel Kaiser; Immo Klose; Rik Oost; James Neuhaus; Nuno Maulide
Journal:  Chem Rev       Date:  2019-06-25       Impact factor: 60.622

2.  A general electron donor-acceptor complex for photoactivation of arenes via thianthrenation.

Authors:  Kai Sun; Anzai Shi; Yan Liu; Xiaolan Chen; Panjie Xiang; Xiaotong Wang; Lingbo Qu; Bing Yu
Journal:  Chem Sci       Date:  2022-04-14       Impact factor: 9.969

3.  Photooxidation of thiosaccharides mediated by sensitizers in aerobic and environmentally friendly conditions.

Authors:  Miqueas G Traverssi; Alicia B Peñéñory; Oscar Varela; Juan P Colomer
Journal:  RSC Adv       Date:  2021-03-01       Impact factor: 3.361

  3 in total

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