Related references
Note: Only part of the references are listed.Transition-Metal-Mediated and -Catalyzed C-F Bond Activation by Fluorine Elimination
Takeshi Fujita et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2019)
Hydrogen Bonding Phase-Transfer Catalysis with Potassium Fluoride: Enantioselective Synthesis of β-Fluoroamines
Gabriele Pupo et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2019)
Organocatalytic Nucleophilic Substitution Reaction of gem-Difluoroalkenes with Ketene Silyl Acetals
Azusa Kondoh et al.
ORGANIC LETTERS (2019)
Copper-catalyzed synthesis of gem-difluoroallylboronates from α-trifluoromethyl alkenes and B2pin2
Xianghu Zhao et al.
TETRAHEDRON LETTERS (2019)
Fluoroalkylation-Borylation of Alkynes: An Efficient Method To Obtain (Z)-Tri- and Tetrasubstituted Fluoroalkylated Alkenylboronates
Wen-Hao Guo et al.
ACS CATALYSIS (2019)
Tyr1-ψ[(Z)CF=CF]-Gly2 Fluorinated Peptidomimetic Improves Distribution and Metabolism Properties of Leu-Enkephalin
Ryan A. Altman et al.
ACS CHEMICAL NEUROSCIENCE (2018)
A Copper(I)-Catalyzed Enantioselective -Boryl Substitution of Trifluoromethyl-Substituted Alkenes: Synthesis of Enantioenriched gamma,gamma-gem-Difluoroallylboronates
Ryoto Kojima et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2018)
Modern Approaches for Asymmetric Construction of Carbon-Fluorine Quaternary Stereogenic Centers: Synthetic Challenges and Pharmaceutical Needs
Yi Zhu et al.
CHEMICAL REVIEWS (2018)
Metal-Free and User-Friendly Regioselective Hydroxyfluorination of Olefins
Daniel M. Sedgwick et al.
ORGANIC LETTERS (2018)
Copper-Catalyzed Stereoselective Defluorinative Borylation and Silylation of gem-Difluoroalkenes
Dong-Hang Tan et al.
ADVANCED SYNTHESIS & CATALYSIS (2018)
Enantioselective Synthesis of Tertiary Allylic Fluorides by Iridium-Catalyzed Allylic Fluoroalkylation
Trevor W. Butcher et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2018)
Recent advances in the synthesis of functionalised monofluorinated compounds
Santos Fustero et al.
CHEMICAL COMMUNICATIONS (2018)
Activation of C-F bonds alpha to C-C multiple bonds
Jean-Denys Hamel et al.
CHEMICAL COMMUNICATIONS (2018)
Copper(I)-catalyzed Stereoselective Defluoroborylation of Aliphatic Gem-Difluoroalkenes
Hajime Ito et al.
CHEMISTRY LETTERS (2018)
Enolizable β-Fluoroenones: Synthesis and Asymmetric 1,2-Reduction
Lukas Zygalski et al.
ORGANIC LETTERS (2018)
Copper-Catalyzed Asymmetric Defluoroborylation of 1-(Trifluoromethyl)Alkenes
Pan Gao et al.
CHEM (2018)
Copper-Catalyzed Regioselective Monodefluoroborylation of Polyfluoroalkenes en Route to Diverse Fluoroalkenes
Hironobu Sakaguchi et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2017)
Synthesis of gem-Difluoroallylboronates via FeCl2-Catalyzed Boration/β-Fluorine Elimination of Trifluoromethyl Alkenes
Yang Liu et al.
ORGANIC LETTERS (2017)
Cu-Catalyzed Stereoselective Borylation of gem-Difluoroalkenes with B2pin2
Juan Zhang et al.
ORGANIC LETTERS (2017)
Highly selective nickel-catalyzed gem-difluoropropargylation of unactivated alkylzinc reagents
Lun An et al.
NATURE COMMUNICATIONS (2017)
Recent progress in the racemic and enantioselective synthesis of monofluoroalkene-based dipeptide isosteres
Myriam Drouin et al.
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY (2017)
Stereoselective Synthesis of Z Fluoroalkenes through Copper-Catalyzed Hydrodefluorination of gem-Difluoroalkenes with Water
Jiefeng Hu et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2017)
Catalytic Asymmetric Mannich Reactions with Fluorinated Aromatic Ketones: Efficient Access to Chiral β-Fluoroamines
Barry M. Trost et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)
Enantioselective fluorination of alpha-branched aldehydes and subsequent conversion to alpha-hydroxyacetals via stereospecific C-F bond cleavage
Kazutaka Shibatomi et al.
CHEMICAL SCIENCE (2016)
Monofluorination of Organic Compounds: 10 Years of Innovation
Pier Alexandre Champagne et al.
CHEMICAL REVIEWS (2015)
Review of recent advances in C-F bond activation of aliphatic fluorides
Qian Shen et al.
JOURNAL OF FLUORINE CHEMISTRY (2015)
Carbon-fluorine bond activation for the synthesis of functionalized molecules
Teresa A. Unzner et al.
TETRAHEDRON LETTERS (2015)
Advances in Catalytic Enantioselective Fluorination, Mono-, Di-, and Trifluoromethylation, and Trifluoromethylthiolation Reactions
Xiaoyu Yang et al.
CHEMICAL REVIEWS (2015)
Functionalization of Fluorinated Molecules by Transition-Metal-Mediated C-F Bond Activation To Access Fluorinated Building Blocks
Theresia Ahrens et al.
CHEMICAL REVIEWS (2015)
Highly Diastereoselective and Enantiospecific Allylation of Ketones and Imines Using Borinic Esters: Contiguous Quaternary Stereogenic Centers
Jack L-Y. Chen et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2014)
Asymmetric Fluorination of α-Branched Cyclohexanones Enabled by a Combination of Chiral Anion Phase-Transfer Catalysis and Enamine Catalysis using Protected Amino Acids
Xiaoyu Yang et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2014)
Catalytic Asymmetric Synthesis of Tertiary Alkyl Fluorides: Negishi Cross-Couplings of Racemic α,α-Dihaloketones
Yufan Liang et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2014)
Synthesis and Applications of α-Trifluoromethylated Alkylboron Compounds
O. Andreea Argintaru et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2013)
Chiral Anion Phase-Transfer Catalysis Applied to the Direct Enantioselective Fluorinative Dearomatization of Phenols
Robert J. Phipps et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2013)
Highly Diastereo- and Enantioselective Allylboration of Aldehydes using α-Substituted Allyl/Crotyl Pinacol Boronic Esters via in Situ Generated Borinic Esters
Jack L. -Y. Chen et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2013)
Synthesis of β-Fluoroamines by Lewis Base Catalyzed Hydrofluorination of Aziridines
Julia A. Kalow et al.
JOURNAL OF ORGANIC CHEMISTRY (2012)
Direct Stereospecific Amination of Alkyl and Aryl Pinacol Boronates
Scott N. Mlynarski et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2012)
NHC-Cu-Catalyzed Enantioselective Hydroboration of Acyclic and Exocyclic 1,1-Disubstituted Aryl Alkenes
Rosa Corberan et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2011)
Iridium-Catalyzed Allylic Fluorination of Trichloroacetimidates
Joseph J. Topczewski et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)
Fluorine & chirality: how to create a nonracemic stereogenic carbon-fluorine centre?
Dominique Cahard et al.
CHEMICAL SOCIETY REVIEWS (2010)
Enantioselective Synthesis of Allylboronates Bearing a Tertiary or Quaternary B-Substituted Stereogenic Carbon by NHC-Cu-Catalyzed Substitution Reactions
Aikomari Guzman-Martinez et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2010)
β-Fluoroamphetamines via the Stereoselective Synthesis of Benzylic Fluorides
Alexander J. Cresswell et al.
ORGANIC LETTERS (2010)
Update 1 of: Asymmetric Fluorination, Trifluoromethylation, and Perfluoroalkylation Reactions
Jun-An Ma et al.
CHEMICAL REVIEWS (2008)
Copper-catalyzed enantioselective substitution of allylic carbonates with diboron:: An efficient route to optically active α-chiral allylboronates
Hajime Ito et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2007)
Diastereomeric fluoroolefins as peptide bond mimics prepared by asymmetric reductive amination of alpha-fluoroenones
Guillaume Dutheuil et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2007)
Stereoselective synthesis of (Z)-fluoroalkenes directed to peptide isosteres:: copper mediated reaction of trialkylaluminum with 4,4-difluoro-5-hydroxyallylic alcohol derivatives
Y Nakamura et al.
TETRAHEDRON (2005)
Regio- and stereoselective synthesis of vicinal fluorohydrins
G Haufe
JOURNAL OF FLUORINE CHEMISTRY (2004)