Synthesis of New Enantiopure Bicyclic 1,2‐Oxazines by Addition of Lithiated Methoxyallene to Chiral Cyclic Nitrones
- 11 March 2003
- journal article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2003 (7) , 1153-1156
- https://doi.org/10.1002/ejoc.200390169
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- 1,2-Oxazines and Their N-Oxides in SynthesisHETEROCYCLES, 2002
- Acid Promoted Syntheses of New Enantiopure Amino Sugar Derivatives from 3,6-Dihydro-2H-1,2-oxazinesSynlett, 2002
- Stereoselective syntheses of heterocycles with lithiated methoxyalleneJournal of Heterocyclic Chemistry, 2000
- A New Diastereoselective Synthesis of Enantiomerically Pure 1,2-Oxazine Derivatives by Addition of Lithiated Methoxyallene to Chiral NitronesSynlett, 1999
- Synthesis and reactivity of α-allenylhydroxylamines: a new efficient access to 3,6-dihydro-1,2-oxazinesChemical Communications, 1998
- Azasugar Syntheses and Multistep Cascade Rearrangements via Hetero Diels-Alder Cycloadditions with Nitroso DienophilesSynlett, 1996
- Tandem [4+2]/[3+2] Cycloadditions of NitroalkenesChemical Reviews, 1996
- A Five-Membered Enantiopure Cyclic Nitrone from Malic Acid by Regioselective Oxidation of Cyclic Hydroxylamine. Synthesis of (1S,7S,8aR)-Octahydro-1,7-dihydroxyindolizineThe Journal of Organic Chemistry, 1995
- Hetero Diels-Alder Reactions with Nitroso Dienophiles: Application to the Synthesis of Natural Product DerivativesSynthesis, 1994
- New synthesis of five-membered cyclic nitrones from tartaric acidThe Journal of Organic Chemistry, 1993