Sucres branchés : Epoxydation stéréospécifique de désoxy-2 méthyléne-2C D-pentoses . Synthése de méthyl glycosides de l'épihamamélose et de l'hamamélose
- 1 January 1978
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 19 (32) , 2869-2872
- https://doi.org/10.1016/s0040-4039(01)94885-3
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Mechanism of the molybdenum and vanadium catalyzed epoxidation of olefins by alkyl hydroperoxidesThe Journal of Organic Chemistry, 1977
- Chiral hydroxamic acids as ligands in the vanadium catalyzed asymmetric epoxidation of allylic alcohols by tert-butyl hydroperoxideJournal of the American Chemical Society, 1977
- Induction asymétrique et cycloadditions[2+1]—IIITetrahedron, 1976
- Unusual stereochemical course of vanadium-catalysed epoxidation of medium-ring allylic alcoholsJournal of the Chemical Society, Chemical Communications, 1976
- Stereoselective epoxidations of acyclic allylic alcohols by transition metal-hydroperoxide reagents. Synthesis of dl-C18 Cecropia juvenile hormone from farnesolJournal of the American Chemical Society, 1974
- Aldolisation dirigee et synthese stereospecifique de doubles liaisons trisubstituees fonctionnalisees.Tetrahedron Letters, 1974
- High stereo- and regioselectivities in the transition metal catalyzed epoxidations of olefinic alcohols by tert-butyl hydroperoxideJournal of the American Chemical Society, 1973
- Verzweigte Zucker, II. Synthese von L‐Streptose und D‐HamameloseEuropean Journal of Inorganic Chemistry, 1972
- 622. Branched-chain sugars. Part IV. The synthesis of D-hamamelose and D-epihamameloseJournal of the Chemical Society, 1965