Directive effects in the opening of epoxides with trimethylsilyl cyanide - zinc iodide. The establishment of three contiguous chiral centers.
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (31), 3259-3262
- https://doi.org/10.1016/s0040-4039(01)81357-5
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Total Synthesis of a Fortimicin AglyconeAngewandte Chemie International Edition in English, 1984
- Ring opening of cyclohexene epoxide with trimethylsilyl cyanideTetrahedron Letters, 1983
- Synthesis of daunosamineThe Journal of Organic Chemistry, 1983
- Asymmetric synthesis of daunosamineThe Journal of Organic Chemistry, 1983
- Stereospecific synthesis of N-benzoyl-L-daunosamine and L-ristosamineThe Journal of Organic Chemistry, 1983
- Opening of epoxides with trimethylsilyl cyanide to produce .beta.-hydroxy isonitriles. A general synthesis of oxazolines and .beta.-amino alcoholsJournal of the American Chemical Society, 1982
- Synthesis of N-benzoyl-Tetrahedron Letters, 1981
- A chiral synthesis of L-acosamine and L-daunosamine via an enantioselective intramolecular[3 + 2]cycloadditionJournal of the American Chemical Society, 1981
- Synthesis of N-trifluoroacetyl-L-acosamine and -L-daunosamineJournal of the Chemical Society, Chemical Communications, 1980
- Synthesis of 3-amino-2,3,6-trideoxy-d-ribo-hexose hydrochlorideCarbohydrate Research, 1976