Diacetoneglucose as Auxiliary Group for the Asymmetric Hetero‐Diels–Alder Reaction with Nitrosoalkenes
- 1 August 1992
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 31 (8) , 1033-1035
- https://doi.org/10.1002/anie.199210331
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Zucker als chirale Auxiliare für die Synthese enantiomerenreiner VerbindungenAngewandte Chemie, 1992
- Asymmetric synthesis of α-amino acids from carbohydrates as chiral templatesTetrahedron, 1991
- Carbohydrates as Chiral Templates: Stereoselective Diels-Alder Synthesis with Dienes of Differing ReactivitySynlett, 1991
- Asymmetric Synthesis of (S)-2-Chloroalkanoic Acids with High Enantiomeric Excess by Diastereoselective Halogenation of α-D-Glucofuranose-Derived Silyl Ketene AcetalsSynlett, 1991
- CorrectionEuropean Journal of Organic Chemistry, 1990
- Enantioselektive Protonierung von Carbanionen mit chiralen ProtonenquellenAngewandte Chemie, 1987
- Diastereoselective Diels–Alder Reaction on Carbohydrate MatricesAngewandte Chemie International Edition in English, 1987
- Diastereoselektive Diels-Alder-Reaktion an Kohlenhydrat-MatricesAngewandte Chemie, 1987
- Arabinose-derived auxiliaries in asymmetric Diels–Alder reactionJournal of the Chemical Society, Chemical Communications, 1987
- Preparation, metallation and alkylation of allenyl ethersRecueil des Travaux Chimiques des Pays-Bas, 1968