Organocatalytic enantioselective Michael-addition of malonic acid half-thioesters to β-nitroolefins: from mimicry of Polyketide synthases to scalable synthesis of γ-amino acids
H. Y. Bae, S. Some, J. H. Lee, J. Kim, M. J. Song, S. Lee, Y. J. Zhang, C. E. Song
Advanced Synthesis & Catalysis, 2011
42
Self-association-free and recyclable, dimeric chinchona alkaloid organocatalysts for methanolytic desymmestrization of meso-glutaric anhydrides
E. H. Nam, S. E. Park, J. S. Oh, S, Some, D. Y. Kim, H. Y. Bae, C. E. Song
Bulletin of the Korean Chemical Society, 2011
43
DOSY NMR for monitoring self aggregation of bifunctional organocatalysts: increasing enantioselectivity with decreasing catalyst concentration
H. B. Jang, H. S. Rho, J. S. Oh, E. H. Nam, S. E. Park, H. Y. Bae, C. E. Song
Organic & Biomolecular Chemistry, 2010
44
Self-association-free dimeric cinchona alkaloid organocatalysts: unprecedented catalytic activity, enantioselectivity and catalyst recyclability in dynamic kinetic resolution of racemic azlactone
J. W. Lee, T. H. Ryu, J. S. Oh, H. Y. Bae, H. B. Jang, C. E. Song
Chemical Communications, 2009
45
SYNTHESIS OF TRIPLE HYDROGEN-BONDING DONOR BEARING N-TRIFLYLPHOSPHORAMIDE AND DERIVATIVES THEREOF
배한용, 송창식, 송선구, 박진현, 이주현, 신명현
, 2024
46
SITAGLIPTIN INTERMEDIATE, METHOD OF SYNTHESIZING THE SITAGLIPTIN INTERMEDIATE, AND METHOD OF SYNTHESIZING SITAGLIPTIN USING THE SITAGLIPTIN INTERMEDIATE
H. Y. Bae, C. E. Song
, 2019
47
METHOD FOR SYNTHESIZING β-AMINO-DITHIOESTER COMPOUND AND β-AMINO-DITHIOESTER COMPOUND SYNTHESIZED BY THE METHOD
H. Y. Bae, C. E. Song
, 2018
48
METHOD FOR PREPARING (R)-ROLIPRAM PRECURSOR BY CATALYTIC ENANTIOSELECTIVE MICAHEL REACTION AND METHOD FOR PREPARING (R)-ROLPTRAM USING THE (R)-ROLIPRAM PRECURSOR
H. Y. Bae, J. Y. Jung, C. E. Song
, 2015
49
METHOD FOR PREPARING (S)-PREGABALIN PRECURSOR BY CATALYTIC ENANTIOSELECTIVE MICAHEL REACTION AND METHOD FOR PREPARING (S)-PREGABALIN USING THE (S)-PREGABALIN PRECURSOR
H. Y. Bae, J. H. Sim, C. E. Song
, 2015
50
METHOD FOR PREPARING CHIAL β-HYDROXY THIOESTER BY CATALYTIC ENANTIOSELECTIVE ALDOL REACTION AND CHIRAL β-HYDROXY THIOESTER SYNTHESIZED BY THE METHODS