Literature DB >> 21919144

Copper-catalyzed trifluoromethylation of unactivated olefins.

Andrew T Parsons1, Stephen L Buchwald.   

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Year:  2011        PMID: 21919144      PMCID: PMC3390945          DOI: 10.1002/anie.201104053

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


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  30 in total

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3.  Structure, Reactivity, and Chemistry of Fluoroalkyl Radicals.

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4.  Novel 10-I-3 hypervalent iodine-based compounds for electrophilic trifluoromethylation.

Authors:  Patrick Eisenberger; Sebastian Gischig; Antonio Togni
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5.  Facile Ar-CF3 bond formation at Pd. Strikingly different outcomes of reductive elimination from [(Ph3P)2Pd(CF3)Ph] and [(Xantphos)Pd(CF3)Ph].

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Journal:  J Am Chem Soc       Date:  2006-10-04       Impact factor: 15.419

6.  Nucleophilic perfluoroalkylation of aldehydes, ketones, imines, disulfides, and diselenides.

Authors:  Chaya Pooput; William R Dolbier; Maurice Médebielle
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7.  Palladium-catalyzed regio- and stereoselective formate reduction of fluorine-containing allylic mesylates. A new entry for the construction of a tertiary carbon attached with a fluoroalkyl group.

Authors:  Tsutomu Konno; Tsuyoshi Takehana; Makoto Mishima; Takashi Ishihara
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8.  New stable reagents for the nucleophilic trifluoromethylation. 1. Trifluoromethylation Of carbonyl compounds with N-formylmorpholine derivatives

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9.  Radical trifluoromethylation of titanium ate enolate.

Authors:  Yoshimitsu Itoh; Koichi Mikami
Journal:  Org Lett       Date:  2005-02-17       Impact factor: 6.005

10.  The first Cu(I)-mediated nucleophilic trifluoromethylation reactions using (trifluoromethyl)trimethylsilane in ionic liquids.

Authors:  Jinwi Kim; Jean'ne M Shreeve
Journal:  Org Biomol Chem       Date:  2004-09-03       Impact factor: 3.876

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  29 in total

1.  Synthesis and applications of α-trifluoromethylated alkylboron compounds.

Authors:  O Andreea Argintaru; DaWeon Ryu; Ioana Aron; Gary A Molander
Journal:  Angew Chem Int Ed Engl       Date:  2013-11-07       Impact factor: 15.336

2.  Allylic functionalization of unactivated olefins with Grignard reagents.

Authors:  Hongli Bao; Liela Bayeh; Uttam K Tambar
Journal:  Angew Chem Int Ed Engl       Date:  2014-01-23       Impact factor: 15.336

Review 3.  Hypervalent Iodine Reagents in High Valent Transition Metal Chemistry.

Authors:  Felipe Cesar Sousa E Silva; Anthony F Tierno; Sarah E Wengryniuk
Journal:  Molecules       Date:  2017-05-12       Impact factor: 4.411

4.  Catalytic One-Step Deoxytrifluoromethylation of Alcohols.

Authors:  Francisco de Azambuja; Sydney M Lovrien; Patrick Ross; Brett R Ambler; Ryan A Altman
Journal:  J Org Chem       Date:  2019-01-25       Impact factor: 4.354

5.  Copper-catalyzed oxytrifluoromethylation of unactivated alkenes.

Authors:  Rong Zhu; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2012-07-23       Impact factor: 15.419

6.  The palladium-catalyzed trifluoromethylation of vinyl sulfonates.

Authors:  Eun Jin Cho; Stephen L Buchwald
Journal:  Org Lett       Date:  2011-11-23       Impact factor: 6.005

7.  Transforming Olefins into γ,δ-Unsaturated Nitriles through Copper Catalysis.

Authors:  Xuesong Wu; Jan Riedel; Vy M Dong
Journal:  Angew Chem Int Ed Engl       Date:  2017-08-10       Impact factor: 15.336

8.  Iron(II)-catalyzed trifluoromethylation of potassium vinyltrifluoroborates.

Authors:  Andrew T Parsons; Todd D Senecal; Stephen L Buchwald
Journal:  Angew Chem Int Ed Engl       Date:  2012-02-10       Impact factor: 15.336

9.  Mechanistic studies on intramolecular C-H trifluoromethoxylation of (hetero)arenes via OCF3-migration.

Authors:  Katarzyna N Lee; Zhen Lei; Cristian A Morales-Rivera; Peng Liu; Ming-Yu Ngai
Journal:  Org Biomol Chem       Date:  2016-06-15       Impact factor: 3.876

10.  Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.

Authors:  Cheng-Liang Zhu; Cheng Wang; Qi-Xue Qin; Sam Yruegas; Caleb D Martin; Hao Xu
Journal:  ACS Catal       Date:  2018-04-20       Impact factor: 13.084

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