Formal Synthesis of 3-Deoxy-d-manno-2-Octulosonic Acid (KDO) via a Highly Double-Stereoselective Hetero Diels−Alder Reaction Directed by a (Salen)CoII Catalyst and Chiral Diene
Author:
Affiliation:
1. State Key Laboratory of Bio-organic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai, 200032, China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo971186w
Reference18 articles.
1. Condensation of Arabinose 5-Phosphate and Phosphorylenol Pyruvate by 2-Keto-3-deoxy-8-phosphooctonic Acid Synthetase
2. Synthesis of 3-Deoxy-D-manno-2-octulosonate-8-phosphate (KDO-8-P) fromD-Arabinose: Generation of D-Arabinose-5-Phosphate using Hexokinase
3. Condensation of D-mannosaldehyde derivatives with ethyl diazoacetate. An easy and stereoselective chain elongation methodology for carbohydrates: Application to new syntheses for KDO and 2-deoxy-β-KDO
4. The furan approach to oxygenated natural products. Total synthesis of (+)-KDO
5. Organic reactions in aqueous media - with a focus on carbon-carbon bond formation
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