Related references
Note: Only part of the references are listed.Asymmetric Synthesis of Dihydrocoumarins through Chiral Phosphoric Acid-Catalyzed Cycloannulation of para-Quinone Methides and Azlactones
Zhi-Pei Zhang et al.
JOURNAL OF ORGANIC CHEMISTRY (2018)
Enantioselective Organocatalytic 1,6-Addition of Aziactones to &ITpara&IT-Quinone Methides: An Access to α,α-Disubstituted and β,β-Diaryl-α-amino acid Esters
Wenjun Li et al.
ORGANIC LETTERS (2018)
Asymmetric 1,6-Conjugate Addition of para-Quinone Methides for the Synthesis of Chiral β,β-Diaryl-α-Hydroxy Ketones
Yuan-Yuan Gao et al.
ADVANCED SYNTHESIS & CATALYSIS (2018)
Asymmetric synthesis of dihydrocoumarins via the organocatalytic hetero-Diels-Alder reaction of ortho-quinone methides
Lili Zhang et al.
ORGANIC & BIOMOLECULAR CHEMISTRY (2017)
Enantioselective Synthesis of Functionalized 4-Aryl Hydrocoumarins and 4-Aryl Hydroquinolin-2-ones via Intramolecular Vinylogous Rauhut-Currier Reaction of para-Quinone Methides
Xiang-Zhi Zhang et al.
ORGANIC LETTERS (2017)
Organocatalytic synthesis of chiral tetrasubstituted allenes from racemic propargylic alcohols
Deyun Qian et al.
NATURE COMMUNICATIONS (2017)
Phosphine-Catalyzed Asymmetric Intermolecular Cross-Vinylogous Rauhut-Currier Reactions of Vinyl Ketones with para-Quinone Methides
Shenhuan Li et al.
ACS CATALYSIS (2017)
Asymmetric synthesis of chromene skeletons via organocatalytic domino reactions of in situ generated ortho-quinone methide with malononitrile and β-functionalized ketone
Lili Zhang et al.
RSC ADVANCES (2017)
Asymmetric Intermolecular Rauhut-Currier Reaction for the Construction of 3,3-Disubstituted Oxindoles with Quaternary Stereogenic Centers
Hongyu Wang et al.
ADVANCED SYNTHESIS & CATALYSIS (2017)
How Understanding the Role of an Additive Can Lead to an Improved Synthetic Protocol without an Additive: Organocatalytic Synthesis of Chiral Diarylmethyl Alkynes
Min Chen et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2017)
Enantioselective Rauhut-Currier-Type 1,6-Conjugate Addition of Methyl Vinyl Ketone to para-Quinone Methides
Tian-Chen Kang et al.
CHEMISTRY-A EUROPEAN JOURNAL (2017)
Catalytic Asymmetric N-Alkylation of Indoles and Carbazoles through 1,6-Conjugate Addition of Aza-para-quinone Methides
Min Chen et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2017)
Phosphoric Acid Catalyzed Asymmetric 1,6-Conjugate Addition of Thioacetic Acid to para-Quinone Methides
Nan Dong et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)
Direct Asymmetric Synthesis of β-Bis-Aryl-α-Amino Acid Esters via Enantioselective Copper-Catalyzed Addition of p-Quinone Methides
Fu-Sheng He et al.
ACS CATALYSIS (2016)
Copper-Catalyzed Borylative Aromatization of p-Quinone Methides: Enantioselective Synthesis of Dibenzylic Boronates
Carlos Jarava-Barrera et al.
ACS CATALYSIS (2016)
Asymmetric Organocatalytic Synthesis of 3-Diarylmethine-Substituted Oxindoles Bearing a Quaternary Stereocenter via 1,6-Conjugate Addition to para-Quinone Methides
Kun Zhao et al.
ACS CATALYSIS (2016)
Organocatalytic Domino Oxa-Michael/1,6-Addition Reactions: Asymmetric Synthesis of Chromans Bearing Oxindole Scaffolds
Kun Zhao et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)
Bifunctional tertiary amine-squaramide catalyzed asymmetric catalytic 1,6-conjugate addition/aromatization of para-quinone methides with oxindoles
Yu-Hua Deng et al.
CHEMICAL COMMUNICATIONS (2016)
Diastereoselective and Enantioselective Synthesis of Unsymmetric β,β-Diaryl-α-Amino Acid Esters via Organocatalytic 1,6-Conjugate Addition of para-Quinone Methides
Xiang-Zhi Zhang et al.
JOURNAL OF ORGANIC CHEMISTRY (2016)
Amide-Phosphonium Salt as Bifunctional Phase Transfer Catalyst for Asymmetric 1,6-Addition of Malonate Esters to para-Quinone Methides
Luo Ge et al.
JOURNAL OF ORGANIC CHEMISTRY (2016)
Chiral phosphoric acid catalyzed asymmetric addition of naphthols to para-quinone methides
Yuk Fai Wong et al.
ORGANIC & BIOMOLECULAR CHEMISTRY (2016)
Organocatalyzed Asymmetric 1,6-Conjugate Addition of para-Quinone Methides with Dicyanoolefins
Xuanyi Li et al.
ORGANIC LETTERS (2016)
Stereoselective 1,6-Conjugate Addition/Annulation of para-Quinone Methides with Vinyl Epoxides/Cyclopropanes
Chao Ma et al.
ACS CATALYSIS (2016)
Copper-Catalyzed Enantioselective 1,6-Boration of para-Quinone Methides and Efficient Transformation of gem-Diarylmethine Boronates to Triarylmethanes
Yazhou Lou et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2015)
Catalytic Asymmetric 1,6-Conjugate Addition of para-Quinone Methides: Formation of All-Carbon Quaternary Stereocenters
Zhaobin Wang et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2015)
para-Quinone Methide: a New Player in Asymmetric Catalysis
Alejandro Parra et al.
CHEMCATCHEM (2015)
Chiral phosphines in nucleophilic organocatalysis
Yumei Xiao et al.
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY (2014)
A New Organocatalytic Concept for Asymmetric α-Alkylation of Aldehydes
Lorenzo Caruana et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2014)
Asymmetric Catalytic 1,6-Conjugate Addition/Aromatization of para-Quinone Methides: Enantioselective Introduction of Functionalized Diarylmethine Stereogenic Centers
Wen-Dao Chu et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2013)
Recent Advances in Organocatalytic Asymmetric Morita-Baylis-Hillman/aza-Morita-Baylis-Hillman Reactions
Yin Wei et al.
CHEMICAL REVIEWS (2013)
Asymmetric anionic polymerizations of 7-cyano-7-alkoxycarbonyl-1,4-benzoquinone methides
Takeshi Nagai et al.
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY (2012)
Asymmetric anionic polymerization of 7-cyano-7-phenyl-1,4-benzoquinone methide
Risa Nakagawa et al.
POLYMER BULLETIN (2012)
Stereocontrol of Optically Active Polymer by Asymmetric Anionic Polymerization of 7-Cyano-7-ethoxycarbonyl-1,4-benzoquinone Methide
Syoko Iizuka et al.
MACROMOLECULES (2010)
Organocatalysis-after the gold rush
Soren Bertelsen et al.
CHEMICAL SOCIETY REVIEWS (2009)
In the golden age of organocatalysis
PI Dalko et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2004)
Polymerizations and polymers of quinonoid monomers
T Itoh
PROGRESS IN POLYMER SCIENCE (2001)
Share Paper
