Enantio- and
Diastereoselective Carbonyl-Ene Cyclization–Acetalization Tandem
Reaction Catalyzed by Tris(Pentafluorophenyl)Borane-Assisted Chiral
Phosphoric Acids
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B(C6F5)3/Chiral Phosphoric
Acid Catalyzed Ketimine–Ene Reaction of 2-Aryl-3H-Indol-3-Ones
and α-Methylstyrenes
10.1002/anie.201915226 · doi-reference
Enantioselective
Synthesis of Spiroimidazolones by Synergistic Catalysis
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Enantioselective
Synthesis of Spirothiazolones via Cooperative Catalysis
10.1002/adsc.202100571 · doi-reference
Formal [3+2] Cycloaddition of Vinylcyclopropane
Azlactones to Enals Using Synergistic Catalysis
10.1039/c8cc06500d · doi-reference
Synergistic Formal Ring Contraction
for the Enantioselective Synthesis of Spiropyrazolones
10.1039/c8sc00913a · doi-reference
Enantioselective
Synthesis of Spiro
Heterocyclic Compounds Using a Combination of Organocatalysis and
Transition-Metal Catalysis
10.1002/tcr.202200284 · doi-reference
Synergistic Palladium-Phosphoric Acid Catalysis in
(3 + 2) Cycloaddition Reactions between Vinylcyclopropanes and Imines
10.3390/catal10020150 · doi-reference
Palladium-Catalyzed
Highly Enantioselective Cycloaddition
of Vinyl Cyclopropanes with Imines
10.1021/acs.orglett.9b00274 · doi-reference
Nickel-Catalyzed Cycloaddition of
Vinylcyclopropanes to Imines
10.1021/ol4005068 · doi-reference
Insertion of Imines
into Vinylcyclopropanes Catalyzed
by Nucleophilic Iron Complexes: A Formal [3+2]-Cycloaddition Strategy
for the Synthesis of Substituted Pyrrolidine Derivatives
10.1055/s-0034-1379180 · doi-reference
Fe-Catalyzed Allylic C–C-Bond
Activation: Vinylcyclopropanes As Versatile A1,A3,D5-Synthons in Traceless
Allylic Substitutions and [3 + 2]-Cycloadditions
10.1021/ja300294a · doi-reference
Vinyl-Aziridines
and Cyclopropanes in Pd-Catalyzed (3+2)-Cycloaddition Reactions with
Cyclic N-Sulfonyl Imines
10.1016/j.tet.2018.09.040 · doi-reference
Palladium(0)-Catalyzed
Diastereoselective (3+2) Cycloadditions of Vinylcyclopropanes with
Sulfonyl-Activated Imines
10.1055/s-0037-1609625 · doi-reference
Pd-Catalyzed
Diastereoselective [3 + 2] Cycloaddition of Vinylcyclopropanes with
Sulfamate-Derived Cyclic Imines
10.1039/c8ob01231h · doi-reference
10.1002/chem.201601893
10.1002/chem.201601893 · doi-reference
Asymmetric
[3 + 2] Cycloaddition of Vinylcyclopropanes and α,β-Unsaturated
Aldehydes by Synergistic Palladium and Organocatalysis
10.1021/acs.orglett.6b00852 · doi-reference
Asymmetric Preparation of Polysubstituted
Cyclopentanes
by Synergistic Pd(0)/Amine Catalyzed Formal [3+2] Cycloadditions of
Vinyl Cyclopropanes with Enals
10.1039/c6cc01775d · doi-reference
Chiral Counteranions in Asymmetric Transition-Metal Catalysis: Highly
Enantioselective Pd/Brønsted Acid-Catalyzed Direct α-Allylation
of Aldehydes
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Selectivity Control
in Enantioselective Four-Component Reactions of Aryl Diazoacetates
with Alcohols, Aldehydes and Amines: An Efficient Approach to Synthesizing
Chiral β-Amino-α-Hydroxyesters
10.1039/b816104f · doi-reference
Cooperative Catalysis with Chiral
Brønsted Acid-Rh2(OAc)4: Highly Enantioselective Three-Component
Reactions of Diazo Compounds with Alcohols and Imines
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Combinations
of Aminocatalysts and Metal Catalysts:
A Powerful Cooperative Approach in Selective Organic Synthesis
10.1021/acs.chemrev.6b00226 · doi-reference
Combining Transition
Metal Catalysis and Organocatalysis–an
Update
10.1039/c2cs35258c · doi-reference
Combining Transition
Metal Catalysis and Organocatalysis: A Broad
New Concept for Catalysis
10.1039/b901258n · doi-reference
Synergistic
Catalysis: A Powerful Synthetic Strategy
for New Reaction Development
10.1039/c2sc00907b · doi-reference
Efficient
Construction of Highly Functionalized Spiro[γ-Butyrolactone-Pyrrolidin-3,3′-Oxindole]
Tricyclic Skeletons via an Organocatalytic 1,3-Dipolar Cycloaddition
10.1039/c3cc40669e · doi-reference
Organocatalytic
Stereocontrolled Synthesis of 3,3′-Pyrrolidinyl Spirooxindoles
by [3+2] Annulation of Isocyanoesters with Methyleneindolinones
10.1039/c2cc30746d · doi-reference
Metal-Free
Asymmetric
1, 3-Dipolar Cycloaddition of N -Arylmaleimides to Azomethine Ylides
Catalyzed by Chiral Tertiary Amine Thiourea
10.1002/ejoc.201100205 · doi-reference
Biomimetic
Asymmetric 1,3-Dioplar
Cycloaddition: Amino Acid Precursors in Biosynthesis Serve as Latent
Azomethine Ylides
10.1021/ol400983j · doi-reference
10.1002/chem.201200358
10.1002/chem.201200358 · doi-reference
Binaphthol-Derived Bisphosphoric
Acids Serve as Efficient Organocatalysts for Highly Enantioselective
1,3-Dipolar Cycloaddition of Azomethine Ylides to Electron-Deficient
Olefins
10.1021/ja204218h · doi-reference
Asymmetic Organocatalytic 1,3-Dipolar
Cycloaddition of Azomethine Ylide to Methyl 2-(2-Nitrophenyl)Acrylate
for the Synthesis of Diastereoisomers of Spirotryprostatin A
10.1021/ol200652j · doi-reference
Organocatalytic Asymmetric Intramolecular [3+2] Cycloaddition:
A Straightforward Approach to Access Multiply Substituted Hexahydrochromeno[4,3-b]Pyrrolidine
Derivatives in High Optical Purity
10.1039/c002369h · doi-reference
Asymmetric Organocatalytic
Formal Double-Arylation of Azomethines for the Synthesis of Highly
Enantiomerically Enriched Isoindolines
10.1039/b917246g · doi-reference
Enantioselective
Organo-SOMO Cycloadditions: A Catalytic Approach to Complex Pyrrolidines
from Olefins and Aldehydes
10.1021/ja305076b · doi-reference
Dynamic One-Pot
Three-Component Catalytic Asymmetric Transformation by Combination
of Hydrogen-Bond-Donating and Amine Catalysts **
10.1002/anie.201101966 · doi-reference
An Amine-Catalyzed
Enantioselective
[3+2] Cycloaddition of Azomethine Ylides and α,β-Unsaturated
Aldehydes: Applications and Mechanistic Implications
10.1002/chem.201103015 · doi-reference
10.1002/adsc.201100432
10.1002/adsc.201100432 · doi-reference
The Organocatalytic [3+2] Cycloaddition
of Azomethine Ylides and α,β-Unsaturated Aldehydes as
a Convenient Tool for the Enantioselective Synthesis of Pyrrolizidines
and Indolizidines
10.1039/c001274b · doi-reference
Organocatalytic Enantioselective
[3 + 2] Cycloaddition of Azomethine Ylides and a, b -Unsaturated Aldehydes**
10.1002/anie.200700988 · doi-reference
