| Literature DB >> 12045352 |
Masao Akagi1, Daichi Omae, Yoshinori Tamura, Tetsujiro Ueda, Tetsuya Kumashiro, Hidehito Urata.
Abstract
L-Ribose was synthesized by a simple four-step method with overall yield of 76.3% from a protected L-arabinose derivative, which is a compatible intermediate for the synthesis of L-deoxyribose. The key step of this strategy is the Swern oxidation and subsequent stereoselective reduction accompanied by inversion of the 2-hydroxy group of protected L-arabinose.Entities:
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Year: 2002 PMID： 12045352 DOI： 10.1248/cpb.50.866
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN： 0009-2363 Impact factor: 1.645