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Synthesis of L-Ribose from D-Ribose by a Stereoconversion through Sequential Lactonization as the Key Transformation

Authors
Ban, JaeyoungShabbir, SairaLim, MinkyungLee, ByunghoonRhee, Hakjune
Issue Date
Sep-2017
Publisher
Georg Thieme Verlag
Keywords
L-ribose; D-ribose; sugar; lactonization; DIBAL-H; reduction
Citation
Synthesis, v.49, no.18, pp.4299 - 4302
Indexed
SCIE
SCOPUS
Journal Title
Synthesis
Volume
49
Number
18
Start Page
4299
End Page
4302
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/9028
DOI
10.1055/s-0036-1588857
ISSN
0039-7881
Abstract
Ribose, a key precursor of various L-nucleosides can only be synthesized from other sugars or other non-sugar precursors. Herein, the study involves the synthesis of naturally rare L-ribose from readily available D-ribose. Though, many synthetic strategies are developed to meet the increasing demands of L-ribose, seeking innovation, a synthesis employing sequential lactonization as the key transformation was explored. This novel conversion involves protection, oxidation, sequential lactonization, reduction with DIBAL-H, and deprotection.
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COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

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COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY (DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING)
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