Organocatalytic [4+2] addition reactions via tetraenamine intermediate

Recent Advances in Asymmetric Organocatalytic Construction of 3,3′-Spirocyclic Oxindoles

(2013) Liang Hong et al.   ADVANCED SYNTHESIS & CATALYSIS

Control of Remote Stereochemistry in the Synthesis of Spirocyclic Oxindoles: Vinylogous Organocascade Catalysis

(2013) Xu Tian et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Remote 1,6-Stereocontrol by Iminium-mediated Organocatalytic Events

(2013) Martin J. Lear et al.   ChemCatChem

Organocatalytic asymmetric remote aziridination of 2,4-dienals

(2013) Kim Søholm Halskov et al.   CHEMICAL COMMUNICATIONS

When asymmetric aminocatalysis meets the vinylogy principle

(2013) Igor D. Jurberg et al.   CHEMICAL COMMUNICATIONS

Zwitterions and Unobserved Intermediates in Organocatalytic Diels–Alder Reactions of Linear and Cross-Conjugated Trienamines

(2013) Arne Dieckmann et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Beyond Classical Reactivity Patterns: Shifting from 1,4- to 1,6-Additions in Regio- and Enantioselective Organocatalyzed Vinylogous Reactions of Olefinic Lactones with Enals and 2,4-Dienals

(2013) Luca Dell’Amico et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Aminocatalytic Enantioselective 1,6 Additions of Alkyl Thiols to Cyclic Dienones: Vinylogous Iminium Ion Activation

(2012) Xu Tian et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Enantioselective H-Bond-Directing Approach for Trienamine-mediated Reactions in Asymmetric Synthesis

(2012) Łukasz Albrecht et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Extending the Aminocatalytic HOMO-Raising Activation Strategy: Where Is the Limit?

(2012) Elena Arceo et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Organocatalytic 1,4-Addition Reaction of α,β-γ,δ-Diunsaturated Aldehydes versus 1,6-Addition Reaction

(2012) Yujiro Hayashi et al.   ChemCatChem

Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones

(2012) Renato Dalpozzo et al.   CHEMICAL SOCIETY REVIEWS

Cross-trienamines in Asymmetric Organocatalysis

(2012) Kim Søholm Halskov et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

The Diarylprolinol Silyl Ether System: A General Organocatalyst

(2011) Kim L. Jensen et al.   ACCOUNTS OF CHEMICAL RESEARCH

exo-Selective Asymmetric Diels-Alder Reaction of 2,4-Dienals and Nitroalkenes by Trienamine Catalysis

(2011) Zhi-Jun Jia et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Quantum Mechanical Investigations of Organocatalysis: Mechanisms, Reactivities, and Selectivities

(2011) Paul Ha-Yeon Cheong et al.   CHEMICAL REVIEWS

Dienamine Catalysis: An Emerging Technology in Organic Synthesis

(2011) Dhevalapally B. Ramachary et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Highly Efficient Hydrogen-Bonding Catalysis of the Diels–Alder Reaction of 3-Vinylindoles and Methyleneindolinones Provides Carbazolespirooxindole Skeletons

(2011) Bin Tan et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Asymmetric Catalysis of Diels–Alder Reactions with in Situ Generated Heterocyclicortho-Quinodimethanes

(2011) Yankai Liu et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Trienamines in Asymmetric Organocatalysis: Diels−Alder and Tandem Reactions

(2011) Zhi-Jun Jia et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Asymmetric Synthesis with Silicon-Based Bulky Amino Organocatalysts

(2010) Li-Wen Xu et al.   ADVANCED SYNTHESIS & CATALYSIS

Asymmetric organocatalysis in total synthesis – a trial by fire

(2010) Eugenia Marqués-López et al.   NATURAL PRODUCT REPORTS

Dihydroazulene Photoswitches: The First Synthetic Protocol for Functionalizing the Seven-Membered Ring

(2009) Michael Åxman Petersen et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Amine-Catalyzed Cyclizations of Tethered α,β-Unsaturated Carbonyl Compounds

(2008) Renata Marcia de Figueiredo et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

The advent and development of organocatalysis

(2008) David W. C. MacMillan   NATURE

Long-range corrected hybrid density functionals with damped atom–atom dispersion corrections

(2008) Jeng-Da Chai et al.   PHYSICAL CHEMISTRY CHEMICAL PHYSICS