Iodocyclisations of allyl- amidines and-ureas
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (24) , 3001-3002
- https://doi.org/10.1016/0040-4039(88)85071-8
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Cyclofunctionalisation reactions of epoxyalcohol derivatives. 3. cyclisationacyl migration of n-benzoylcarbamates to stereodefined oxazolidinones. A new, diastereospecific route to thiamphenicol.Tetrahedron Letters, 1987
- Factors affecting the regioselection of allylic imidate iodocyclizationThe Journal of Organic Chemistry, 1986
- A procedure for “iodolactamization”Tetrahedron Letters, 1985
- Two-step synthesis of imidazoles from activated alkynesJournal of the Chemical Society, Perkin Transactions 1, 1985
- Carbamate mediated functionalization of unsaturated alcohols II. Regio- and stereo-selective synthesis of 1,3-syn and 1,2-anti amino alcohol derivatives via iodocarbamationTetrahedron Letters, 1984
- Synthesis of imidazoles from alkenesJournal of the Chemical Society, Perkin Transactions 1, 1984
- Trichloroacetamidines, a new class of positive inotropic agentsJournal of Medicinal Chemistry, 1978
- Cyclic amidines. Part XXIV. Cyclisation of N-allyl-N′-arylacetamidines to imidazolines, dihydroquinazolines, and dihydrobenzodiazepinesJournal of the Chemical Society, Perkin Transactions 1, 1973