Highly stereoselective addition of 2-trimethylsilyloxyfuran to N-glyoxyloyl-(2R)-bornane-10,2-sultam
- 30 April 1996
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 7 (4) , 981-984
- https://doi.org/10.1016/0957-4166(96)00097-3
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Highly stereoselective total synthesis of octopyranose derivativesTetrahedron, 1991
- The four-carbon elongation of aldehydo sugars using 2-(trimethylsiloxy)furan: a butenolide route to higher monosaccharidesThe Journal of Organic Chemistry, 1990
- The four-carbon elongation of three-carbon chiral synthons using 2-(trimethylsiloxy)furan: highly stereocontrolled entry to enantiomerically pure seven-carbon α,β-unsaturated 2,3-dideoxy-aldonolactonesTetrahedron, 1990
- Diastereoselective synthesis of the lactone portion of compactin and mevinolinJournal of the Chemical Society, Chemical Communications, 1990
- Asymmetric Diels‐Alder Reaction of 1‐Methoxybuta‐1,3‐diene with (2R)‐N‐Glyoxyloylbornane‐10,2‐sultamHelvetica Chimica Acta, 1989
- Organic Syntheses under High Pressure: Lanthanide-Catalysed [4 + 2]Cycloaddition of 1-Methoxybuta-1,3-diene to Carbonyl CompoundsSynthesis, 1985
- Camphor‐Derived N‐Acryloyl and N‐Crotonoyl Sultams: Practical Activated Dienophiles in Asymmetric Diels‐alder Reactions. Preliminary CommunicationHelvetica Chimica Acta, 1984