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Chemical Society Reviews, ISSN 0306-0012, 09/2011, Volume 40, Issue 9, pp. 4539 - 4549
Chiral phosphoric acids and derivatives have attracted considerable attention as a powerful tool in asymmetric catalysis. Various enantioselective reactions... 
MUKAIYAMA-ALDOL | BAEYER-VILLIGER REACTION | PHOSPHORIC-ACID | NAZAROV CYCLIZATION | HETERO-DIELS-ALDER | ALDEHYDES | CATALYST | FRIEDEL-CRAFTS ALKYLATION | CHEMISTRY, MULTIDISCIPLINARY | 3-SUBSTITUTED CYCLOBUTANONES | MICHAEL ADDITION
Journal Article
11/2012
Asymmetric catalysis is one of the most effective ways to control a target molecule’s stereochemistry. Through the development of a wide variety of chiral... 
Chiral Ligand | Hetero-Diels-Alder | Dithiolenes | 0488 | Asymmetric Catalysis | Platinum | Palladium | Ligand Non Innocence
Dissertation
Chemistry Letters, ISSN 0366-7022, 2018, Volume 47, Issue 2, pp. 144 - 147
Journal Article
Synthesis, ISSN 0039-7881, 10/2014, Volume 46, Issue 20, pp. 2701 - 2710
Abstract The recent development of several sulfur dioxide surrogates has seen a renaissance in its chemistry, with a number of new synthetic methods being... 
short review | sulfinate | sulfur dioxide | surrogate | sulfonamide | metal catalysis | sulfone | ORGANIC-CHEMISTRY | 3-COMPONENT SYNTHESIS | ONE-POT | SULFONE SYNTHESIS | CHEMISTRY, ORGANIC | CHARGE-TRANSFER COMPLEXES | MOLECULAR-COMPLEXES | ENE REACTION | HETERO-DIELS-ALDER | CHELETROPIC ADDITIONS | TRIOXIDE COMPLEXES
Journal Article
Organic Letters, ISSN 1523-7060, 05/2016, Volume 18, Issue 9, pp. 2200 - 2203
A base promoted, protection-free, and regioselective synthesis of highly functionalized quinolines via [4 + 2] cycloaddition of azadienes (generated in situ... 
FACILE SYNTHESIS | TANDEM SYNTHESIS | ANNULATION | REGIOSELECTIVE SYNTHESIS | CHEMISTRY, ORGANIC | HETERO-DIELS-ALDER | PROPARGYL ALCOHOLS | PYRIDINES | HYDROAMINATION | POLYSUBSTITUTED QUINOLINES | SUBSTITUTED QUINOLINES
Journal Article
Organic Letters, ISSN 1523-7060, 06/2010, Volume 12, Issue 11, pp. 2476 - 2479
The first Brønsted acid catalyzed asymmetric Mukaiyama aldol reaction of aldehydes using silyl enol ethers of ketones as nucleophiles has been reported. A... 
CHEMISTRY, ORGANIC | HETERO-DIELS-ALDER | ACTIVATION | CHIRAL BRONSTED ACID | LEWIS-ACID
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 10/2016, Volume 81, Issue 19, pp. 8911 - 8919
An efficient protocol for the direct transformation of chroman-4-ones to tricyclic fused pyridines with the skeleton of cassiarins, a family of alkaloids with... 
ANTITUMOR AGENTS | CATALYZED INTRAMOLECULAR ANNULATION | DIVERSITY-ORIENTED SYNTHESIS | PRIVILEGED STRUCTURES | DRUG DISCOVERY | CHEMISTRY, ORGANIC | HETERO-DIELS-ALDER | BOND ACTIVATION | CHEMICAL SPACE | CASSIA-SIAMEA | RHODIUM CATALYSIS
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 6/2018, Volume 47, Issue 12, pp. 4388 - 448
Recent developments in catalytic asymmetric aldol reactions have been summarized. Enantioselective aldol reactions are important methods to synthesize... 
CHIRAL FERROCENYLAMINE LIGANDS | LEWIS-ACID CATALYSTS | DIRECT ASYMMETRIC ALDOL | SOLVENT-FREE CONDITIONS | SUPPORTED L-PROLINE | SILYL ENOL ETHERS | ALPHA-AMINO-ACIDS | HETERO-DIELS-ALDER | C-SYMMETRIC COPPER(II) COMPLEXES | CHEMISTRY, MULTIDISCIPLINARY | POLY(ETHYLENE GLYCOL)-SUPPORTED PROLINE
Journal Article
Chemistry - A European Journal, ISSN 0947-6539, 2014, Volume 20, Issue 42, p. 13644
  In view of increasing demands for efficient photosensitizers for photodynamic therapy (PDT), we herein report the synthesis and photophysical... 
Porphyrinoids | Hetero Diels-Alder | Photophysics | Chlorine | Knoevenagel | Spectrum analysis
Journal Article
Chemistry Letters, ISSN 0366-7022, 2/2018, Volume 47, Issue 2, pp. 144 - 147
A synthetic route to α-aminoketone derivatives via a hetero Diels–Alder reaction is described. Diacylhydrazine was oxidized by tert-butyl hypochlorite in the... 
Hetero Diels-Alder reaction | KETONES | AMINATION | CATALYZED OXIDATION | Azodicarbonyl compound | alpha-Aminocarbonyl compound | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2017, Volume 56, Issue 18, pp. 4936 - 4940
Journal Article