Synthetic and Mechanistic Studies on Pd(0)-Catalyzed Diamination of Conjugated Dienes
نویسندگان
چکیده
منابع مشابه
Cyclopolymerization of Conjugated Dienes
The formation of essentially saturated polymers containing fused cyclohexane rings is a characteristic of the polymerization of conjugated dienes under the influence of all cationic or Lewis acid catalysts. The amount of cyclic structures and non-terminal linear unsaturation is dependent upon the electron accepting ability of the catalyst, which may be greatly influenced by the nature of the so...
متن کاملA mild, palladium-catalyzed method for the dehydrohalogenation of alkyl bromides: synthetic and mechanistic studies.
We have exploited a typically undesired elementary step in cross-coupling reactions, β-hydride elimination, to accomplish palladium-catalyzed dehydrohalogenations of alkyl bromides to form terminal olefins. We have applied this method, which proceeds in excellent yield at room temperature in the presence of a variety of functional groups, to a formal total synthesis of (R)-mevalonolactone. Our ...
متن کاملPalladium-Catalyzed Nucleophilic Substitution of Alcohols: Mechanistic Studies and Synthetic Applications
Sawadjoon, S. 2013. Palladium-Catalyzed Nucleophilic Substitution of Alcohols. Mechanistic Studies and Synthetic Applications. Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 1092. 63 pp. Uppsala: Acta Universitatis Upsaliensis. ISBN 978-91-554-8785-0. This thesis deals with the palladium-catalyzed nucleophilic substitution of π-activated alco...
متن کاملChemoselective Pd-catalyzed oxidation of polyols: synthetic scope and mechanistic studies.
The regio- and chemoselective oxidation of unprotected vicinal polyols with [(neocuproine)Pd(OAc)]2(OTf)2 (1) (neocuproine = 2,9-dimethyl-1,10-phenanthroline) occurs readily under mild reaction conditions to generate α-hydroxy ketones. The oxidation of vicinal diols is both faster and more selective than the oxidation of primary and secondary alcohols; vicinal 1,2-diols are oxidized selectively...
متن کاملPalladium-Catalyzed Intra- and Intermolecular C–H Arylation Using Mesylates: Synthetic Scope and Mechanistic Studies
This paper describes the development of Pd-catalyzed inter- and intramolecular direct arylation using mesylates. Furthermore, a sequential mesylation/arylation protocol using phenols as substrates is described. These transformations are general with respect to the electronics of the C-H substrates and allow for the synthesis of diverse heterocyclic motifs in good yields. Both arenes and heteroa...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of the American Chemical Society
سال: 2010
ISSN: 0002-7863,1520-5126
DOI: 10.1021/ja909459h