Journal of Synthetic Organic Chemistry, Japan
Online ISSN : 1883-6526
Print ISSN : 0037-9980
ISSN-L : 0037-9980
Reviews and Accounts
Recent Progress in the Boron-Mediated Aglycon Delivery: Reaction Development, Synthesis of Useful Glycosides, and Its Application to Chemical Biology
Daisuke TakahashiKazunobu Toshima
Author information
JOURNAL RESTRICTED ACCESS

2024 Volume 82 Issue 9 Pages 856-866

Details
Abstract

There are many glycosides with 1,2-cis-O-glycosidic linkages (1,2-cis glycosides) in biologically active natural products and drugs. The development of new lead compounds for drugs by elucidating the mechanisms of their biological activities and developing their structures has attracted attention. However, the stereoselective synthesis of 1,2-cis-glycosides is still a challenging task due to the lack of general methods corresponding to the neighboring group participation method for the 1,2-trans-stereoselective glycosylation. In this context, we have developed organoboron-catalyzed regio- and 1,2-cis-stereoselective glycosylation method, namely, boron-mediated aglycon delivery (BMAD). This review article describes the recent progress in the BMAD method since our review article published in this journal in 2020, including (1) diastereoselective desymmetric BMAD reaction of meso-diols, (2) BMAD reaction of trans-1,2-diols using a diboron catalyst, (3) total synthesis of terpioside B using BMAD reaction, (4) β-arabinofuranosylation using BMAD reaction, and (5) chemical-biological studies using late-stage BMAD reaction.

Graphical Abstract Fullsize Image
Content from these authors
© 2024 The Society of Synthetic Organic Chemistry, Japan
Previous article Next article
feedback
Top