Stereoselective iodolactonization of acyclic unsaturated 3-hydroxyacids
- 1 January 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (46) , 4611-4614
- https://doi.org/10.1016/s0040-4039(01)82994-4
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- A highly efficient asymmetric synthesis of optically active α,β-epoxyaldehydes from α,β-unsaturated acidsTetrahedron Letters, 1980
- Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesisTetrahedron, 1980
- Asymmetric halolactonisation reaction-2Tetrahedron, 1979
- Asymmetric halolactonisation reaction—1Tetrahedron, 1979
- Synthesis and synthetic utility of halolactonesChemical Society Reviews, 1979
- Stereoselective epoxidation of acyclic olefinic carboxylic acids via iodolactonizationJournal of the American Chemical Society, 1978
- Asymmetric halolactonization reaction: a highly efficient synthesis of optically active α-hydroxy acids from α,β-unsaturated acidsTetrahedron Letters, 1977
- Formation of β-lactones in the iodolactonization reactionTetrahedron Letters, 1972
- Metalated carboxylic acids. IV. Reactions of metalated carboxylic acids with epoxides. Substituted steroidal spiro .gamma.-lactones from spiro .beta.-epoxidesThe Journal of Organic Chemistry, 1972
- The total syntheses of 2-deoxy-DL- and L-ribosesTetrahedron Letters, 1967