Stereospecific additions to olefins. Synthetic utility of nitrilium ion intermediates
- 1 January 1966
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 7 (27) , 3119-3123
- https://doi.org/10.1016/s0040-4039(01)99925-3
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Additions of Iodine Azide to Olefins. Stereospecific Introduction of Azide Functions1Journal of the American Chemical Society, 1965
- Synthese von Imidazolinen und Imidazolidinen durch Reaktion von Aziridinium-tetrafluoroborat mit Nitrilen und BenzylidenanilinAngewandte Chemie, 1965
- Synthesis and Ring Opening of Fused Steroidal Aziridines*,1The Journal of Organic Chemistry, 1965
- Small Charged Rings. VI. Expansion of the Aziridinium Ring by Reaction with Nitriles. A New Type of Benzylating Agent1-3The Journal of Organic Chemistry, 1965
- A new synthesis of 1,5-dialkyl tetrazoles from nitrilium salts and sodium azideTetrahedron Letters, 1965
- Stereospecific additions to olefins. The iodonium ionTetrahedron Letters, 1964
- CONTRIBUTION TO THE INFRARED SPECTRA OF FIVE-MEMBERED N- AND N,S-HETEROCYCLIC COMPOUNDSCanadian Journal of Chemistry, 1964
- THE REACTION OF ISOXAZOLIUM SALTS WITH BASESJournal of the American Chemical Society, 1961
- A NEW REACTION OF OLEFINS, NITRILES, AND HALOGENS1The Journal of Organic Chemistry, 1952
- A New Reaction of Nitriles. I. Amides from Alkenes and Mononitriles1Journal of the American Chemical Society, 1948