Stereoselective cycloaddition of 1-glucosyl-1,3-butadienes with tert-butyl 2H-azirine-3-carboxylate, glyoxylates and imines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Asymmetric Diels–Alder reactions. Part 3. Influence of butadiene structure upon the diastereofacial reactivity of (E)-1-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyloxy)buta-1,3-dienes
2. Asymmetric Diels–Alder reactions. Part 2. A model to account for the diastereofacial reactivity of (E)-1-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyloxy)-3-trimethylsiloxybuta-1,3-diene and its 2-methyl derivative. X-Ray molecular structure of (E)-1-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyloxy)-3-trimethylsiloxybuta-1,3-diene and of (1R,6R,9R,10S)-9-methyl-10-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyloxy)bicyclo[4.4.0]dec-3-ene-2,5,8-trione
3. Generation and Diels-Alder reactions of t-butyl 2H-azirine-3-carboxylate
4. Diastereoselective synthesis of aziridines from (1R)-10-(N,N-dialkylsulfamoyl)isobornyl 2H-azirine-3-carboxylates
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