New multi-coupling benzylic zinc reagents for the preparation of flexible aromatic compounds
- 1 March 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (10) , 1749-1752
- https://doi.org/10.1016/s0040-4039(97)00187-1
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Selective Pd(0)-Catalyzed Arylations with New Electrophilic or Nucleophilic Multi-Coupling ReagentsSynlett, 1996
- Preparation and reactions of polyfunctional organozinc reagents in organic synthesisChemical Reviews, 1993
- Transition metal catalyzed reactions of organozinc reagentsTetrahedron, 1992
- Palladium-catalyzed coupling of aryl triflates with organostannanesJournal of the American Chemical Society, 1987
- 2′‐Nitro‐2′‐propen‐1′‐yl 2,2‐Dimethylpropanoate (NPP), A Multiple Coupling ReagentHelvetica Chimica Acta, 1984
- Synthesis and reactions of substituted nitro-allylating reagentsTetrahedron Letters, 1982
- Palladium- or nickel-catalyzed cross coupling. A new selective method for carbon-carbon bond formationAccounts of Chemical Research, 1982
- Palladium-catalyzed cross-coupling reaction of homoallylic or homopropargylic organozincs with alkenyl halides as a new selective route to 1,5-dienes and 1,5-enynesJournal of the American Chemical Society, 1980
- Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halidesThe Journal of Organic Chemistry, 1977
- Highly general stereo-, regio-, and chemo-selective synthesis of terminal and internal conjugated enynes by the Pd-catalysed reaction of alkynylzinc reagents with alkenyl halidesJournal of the Chemical Society, Chemical Communications, 1977