Total synthesis of both enantiomers of trans-2,3-cis-3,4-dihydroxyproline
- 30 April 1996
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 7 (4) , 1167-1180
- https://doi.org/10.1016/0957-4166(96)00123-1
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Furan-, Pyrrole-, and Thiophene-Based Siloxydienes for Syntheses of Densely Functionalized Homochiral CompoundsSynthesis, 1995
- γ-Substituted pyrrole-based silyl dienol ethers as α-amino acid enolate equivalents: a versatile entry to racemic α-substituted α-amino acidsJournal of the Chemical Society, Perkin Transactions 1, 1995
- Total syntheses of N-boc-protected 3′-deoxy-4′-azathymidine and 4′-azauridineTetrahedron Letters, 1994
- Total Syntheses of All Four Isomers of cis-1,2-DihydroxypyrrolizidineThe Journal of Organic Chemistry, 1994
- General approach to hydroxylated α-amino acids exploiting N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrroleJournal of the Chemical Society, Perkin Transactions 1, 1994
- Selective reactions using N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole: concise asymmetric syntheses of (+)-1-deoxy-8-epi-castanospermine and its enantiomerJournal of the Chemical Society, Perkin Transactions 1, 1993
- Homochiral α,β-unsaturated γ-lactams: Versatile templatesTetrahedron: Asymmetry, 1992
- N-(tert-Butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole: a promising compound for synthesis of chiral nonracemic hydroxylated pyrrolidine derivativesThe Journal of Organic Chemistry, 1992
- Synthesis of (2R,3S,4R)-3,4-dihydroxyproline from D-ribonolactone; an approach to the synthesis of polyfunctionalised D-amino acids from sugar lactones. X-Ray molecular structures of 2-azido-3,4-O-(R)-benzylidene-2-deoxy-D-ribono-1,5-lactone, 2-azido-2-deoxy-D-ribono-1,4-lactone, and (2R,3S,3R)-3,4-dihydroxyprolineJournal of the Chemical Society, Perkin Transactions 1, 1987
- Synthesis of 2R,3S,4R-dihydroxyproline from D-ribonolactoneTetrahedron Letters, 1986