| Literature DB >> 26368916 |
Chintada Nageswara Rao1, Christoph Bentz1, Hans-Ulrich Reissig2.
Abstract
New conditions for dearomatizing samarium-ketyl (hetero)arene cyclizations are reported. In many examples of these samarium diiodide-mediated reactions, lithium bromide and water can be used as additives instead of the carcinogenic and mutagenic hexamethylphosphoramide (HMPA). The best results were obtained for the cyclizations of N-acylated indole derivatives delivering the expected indolines in good yields and excellent diastereoselectivities. A new type of cyclization delivering indolyl-substituted allene derivatives is also described. The scope and limitations of the lithium bromide/water system are discussed.Entities:
Keywords: cyclization; indoles; radicals; reductions; samarium diiodide; solvent effects
Year: 2015 PMID: 26368916 DOI: 10.1002/chem.201502912
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236