Literature DB >> 26568447

Regioselective modification of unprotected glycosides.

Manuel Jäger1, Adriaan J Minnaard1.   

Abstract

Selective modification of unprotected carbohydrates is difficult due to the similar reactivity of the hydroxyl groups. In carbohydrate synthesis, therefore, even straightforward transformations often require multiple synthetic steps. The development of selective methods for carbohydrate modification is consequently highly desired. This review describes the methods for the regio- and chemoselective carbohydrate modification, with a focus on novel approaches that mainly apply transition metal catalysis and organocatalysis, and discusses the challenges and opportunities in this field.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 26568447     DOI: 10.1039/c5cc08199h

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  11 in total

1.  Picoloyl protecting group in synthesis: focus on a highly chemoselective catalytic removal.

Authors:  Scott A Geringer; Michael P Mannino; Mithila D Bandara; Alexei V Demchenko
Journal:  Org Biomol Chem       Date:  2020-07-01       Impact factor: 3.876

Review 2.  Synthesis of carbohydrate building blocks via regioselective uniform protection/deprotection strategies.

Authors:  Tinghua Wang; Alexei V Demchenko
Journal:  Org Biomol Chem       Date:  2019-05-02       Impact factor: 3.876

3.  Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2.

Authors:  Tinghua Wang; Swati S Nigudkar; Jagodige P Yasomanee; Nigam P Rath; Keith J Stine; Alexei V Demchenko
Journal:  Org Biomol Chem       Date:  2018-05-15       Impact factor: 3.876

4.  Rapid assembly of branched mannose oligosaccharides through consecutive regioselective glycosylation: A convergent and efficient strategy.

Authors:  Bo Meng; Jun Wang; Qianli Wang; Anthony S Serianni; Qingfeng Pan
Journal:  Tetrahedron       Date:  2017-05-22       Impact factor: 2.457

5.  Synthesis of 2-azido-2-deoxy- and 2-acetamido-2-deoxy-D-manno derivatives as versatile building blocks.

Authors:  Catherine Alex; Satsawat Visansirikul; Yongzhen Zhang; Jagodige P Yasomanee; Jeroen Codee; Alexei V Demchenko
Journal:  Carbohydr Res       Date:  2019-12-23       Impact factor: 2.104

6.  Regioselective Carbohydrate Oxidations: A Nuclear Magnetic Resonance (NMR) Study on Selectivity, Rate, and Side-Product Formation.

Authors:  Niek N H M Eisink; Martin D Witte; Adriaan J Minnaard
Journal:  ACS Catal       Date:  2017-01-18       Impact factor: 13.084

7.  From d- to l-Monosaccharide Derivatives via Photodecarboxylation-Alkylation.

Authors:  I C Steven Wan; Martin D Witte; Adriaan J Minnaard
Journal:  Org Lett       Date:  2019-09-12       Impact factor: 6.005

8.  Protecting group free glycosylation: one-pot stereocontrolled access to 1,2-trans glycosides and (1→6)-linked disaccharides of 2-acetamido sugars.

Authors:  Xin Qiu; Anna L Garden; Antony J Fairbanks
Journal:  Chem Sci       Date:  2022-03-17       Impact factor: 9.825

9.  Synthesis and glycosidation of building blocks of D-altrosamine.

Authors:  Mariya Novakova; Anupama Das; Catherine Alex; Alexei V Demchenko
Journal:  Front Chem       Date:  2022-09-26       Impact factor: 5.545

10.  Site-switchable mono-O-allylation of polyols.

Authors:  Hua Tang; Yu-Biao Tian; Hongyan Cui; Ren-Zhe Li; Xia Zhang; Dawen Niu
Journal:  Nat Commun       Date:  2020-11-10       Impact factor: 14.919

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.