IPy2BF4 is also a useful reagent for stereospecific iodine-silicon exchange in open chain trimethylsilylalkenes
- 20 March 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (12) , 2153-2156
- https://doi.org/10.1016/0040-4039(95)00199-m
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- 1‐Iodoalkynes Can Also Be Dimerized: A New Head‐to‐Tail CouplingAngewandte Chemie International Edition in English, 1993
- Acid-mediated reaction of bis(pyridine)iodonium(I) tetrafluoroborate with aromatic compounds. A selective and general iodination methodThe Journal of Organic Chemistry, 1993
- Electrophilic additions of positive iodine to alkynes through an iodonium mechanismThe Journal of Organic Chemistry, 1990
- Non-ipso electrophilic substitution of vinylstannanes and silanesJournal of the Chemical Society, Chemical Communications, 1989
- Silafunctional compounds in organic synthesis. 32. Stereoselective halogenolysis of alkenylsilanes: stereochemical dependence on the coordination state of the leaving silyl groupsThe Journal of Organic Chemistry, 1987
- Vinylsilane- and alkynylsilane-terminated cyclization reactionsChemical Reviews, 1986
- Friedel-Crafts reactions of some vinylsilanesJournal of the Chemical Society, Perkin Transactions 1, 1980
- A highly stereoselective synthesis of vinyl bromides and chlorides via disubstituted vinylsilanesThe Journal of Organic Chemistry, 1978
- Reaction of deuterium chloride with cis- and trans-.beta.-trimethylsilylstyreneJournal of the American Chemical Society, 1973
- The Reactivity with Alkali of Chlorine—Carbon Bonds Alpha, Beta and Gamma to Silicon1,2Journal of the American Chemical Society, 1946