4H-pyran derivatives show diverse biological activity such as antimicrobial, antibacterial, antiviral and antifungal. 4H-pyran derivatives can be synthesized easily from 2-(3-oxo-1,3-diphenylpropyl)malononitrile which is the Michael addition product of malononitrile to trans-chalcone. Synthesizing chiral biologically active compounds with metal free approach (organocatalysis) is a significant topic. In this thesis, chiral 2-(3-oxo-1,3-diphenylpropyl)malononitrile was synthesized with quinine or 2-aminoDMAP based novel bifunctional organocatalysts which were developed in our group. In the asymmetric Michael addition reaction, 2-adamantyl anchored quinine-squaramide organocatalyst was found the best among the other tested organocatalysts in t...
A simple chiral diamine catalyst (<b>1a</b>) was successfully applied in the asymmetric Michael reac...
The first cinchona-alkaloid-organocatalyzed enantioselective synthesis of chiral 1,4-dihydropyridine...
Function-oriented design and synthesis of chiral small molecules with novel activity is a key goal i...
The decarboxylative Michael and aldol reactions are quite new in the asymmetric studies and are used...
A highly enantioselective one-pot synthesis of important building blocks, α-chiral γ-keto esters, ha...
Organocatalytic asymmetric reactions are efficient and environmentally friendly methods to synthesiz...
The first efficient and highly enantioselective Michael addition–protonation reaction of malononitri...
A family of 9-amino(9-deoxy) epicinchonine derivatives, possessing a range of mono- and bidentate hy...
Chiral derivatives of γ-aminobutyric acid are widely used as medicines and can be obtained by organo...
Highly enantioselective biomimetic Michael addition reactions of malonic acid half thioesters (MAHTs...
In this work, we describe the Michael addition–cyclization reaction of 2-(2-nitrovinyl)phenol with t...
An efficient and convenient highly enantioselective Michael addition of malononitrile to enones ha...
Cascade reactions of 1,3-dicarbonyls with Morita–Baylis–Hillman acetates of nitroalkenes using a qui...
Efficient synthesis of non-annulated 2-amino-4H-pyrans and 2-amino-8-oxo-4,8-dihydropyrano[3,2-b]pyr...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...
A simple chiral diamine catalyst (<b>1a</b>) was successfully applied in the asymmetric Michael reac...
The first cinchona-alkaloid-organocatalyzed enantioselective synthesis of chiral 1,4-dihydropyridine...
Function-oriented design and synthesis of chiral small molecules with novel activity is a key goal i...
The decarboxylative Michael and aldol reactions are quite new in the asymmetric studies and are used...
A highly enantioselective one-pot synthesis of important building blocks, α-chiral γ-keto esters, ha...
Organocatalytic asymmetric reactions are efficient and environmentally friendly methods to synthesiz...
The first efficient and highly enantioselective Michael addition–protonation reaction of malononitri...
A family of 9-amino(9-deoxy) epicinchonine derivatives, possessing a range of mono- and bidentate hy...
Chiral derivatives of γ-aminobutyric acid are widely used as medicines and can be obtained by organo...
Highly enantioselective biomimetic Michael addition reactions of malonic acid half thioesters (MAHTs...
In this work, we describe the Michael addition–cyclization reaction of 2-(2-nitrovinyl)phenol with t...
An efficient and convenient highly enantioselective Michael addition of malononitrile to enones ha...
Cascade reactions of 1,3-dicarbonyls with Morita–Baylis–Hillman acetates of nitroalkenes using a qui...
Efficient synthesis of non-annulated 2-amino-4H-pyrans and 2-amino-8-oxo-4,8-dihydropyrano[3,2-b]pyr...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...
A simple chiral diamine catalyst (<b>1a</b>) was successfully applied in the asymmetric Michael reac...
The first cinchona-alkaloid-organocatalyzed enantioselective synthesis of chiral 1,4-dihydropyridine...
Function-oriented design and synthesis of chiral small molecules with novel activity is a key goal i...