1990 年 48 巻 4 号 p. 304-318
This article reviews our own work on the recent development of the methodology for chiral preparation of nitrogen-containing natural products including alkaloids, antibiotics etc. utilizing 4-O-benzyl-2, 3-O-bis (methoxymethyl) -L-threitol (1), readily available from L-tartaric acid, as a common chiral synthon. The strategy for the natural product synthesis is based on regulating the stereochemical course of nucleophilic addition to the α, β-bis [(methoxymethyl) oxy] carbonyl and imino systems with highly selective diastereofacial differentiation in chelation or nonchelation processes, which are predictable. Also, this approach has allowed us to demonstrate the marked versatility of 1 as a synthetically very flexible chiral building block.