Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate: An efficient preparation of a synthetic intermediate of cyclopropane amino acids
- 31 March 1995
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 6 (3) , 691-692
- https://doi.org/10.1016/0957-4166(95)00063-u
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Diastereoselective iodocarbocyclization of 4-pentenylmalonate derivatives: Application to cyclosarkomycin synthesisTetrahedron Letters, 1994
- Synthesis of Cyclopropane Amino Acids and Their Incorporation into Bioactive Peptides as Conformational Constraint.Journal of Synthetic Organic Chemistry, Japan, 1994
- Ionic iodocarbocyclization reactions of 4-alkenyl- and 4-alkynylmalonate derivativesThe Journal of Organic Chemistry, 1993
- Asymmetric syntheses of all four stereoisomers of 2,3-methanomethionineThe Journal of Organic Chemistry, 1992
- Ionic iodocarbocyclization reactionTetrahedron Letters, 1992
- An Enzymatic Enantioselective Route to Methyl Carboxylate 2,3 - Methanohomoserine γ-Lactone; A Precursor of Chiral 2,3 - MethanohomoserineSynthetic Communications, 1991
- Cyclopropane amino acidsTetrahedron, 1990
- Ethylene Biosynthesis part 10. Synthesis and study of racemic, (1R, 2S)-, and (1S, 2R)-1-Amino-2-(hydroxymethyl)cyclopropanecarboxylic AcidHelvetica Chimica Acta, 1989
- Stereoselective Synthesis of Enantiomerically Pure Natural Products—Estrone as ExampleAngewandte Chemie International Edition in English, 1983
- Asymmetric Total Synthesis of (+)‐EstroneAngewandte Chemie International Edition in English, 1980