Enantioselective Synthesis of the C20-C25 Portion of the Cytotoxic Natural Product, Amphidinolide B1
이덕형
Bull. Kor. Chem. Soc., 199806
52
A Facile Synthesis of N-Carbamoylmethyl-a-aminobutyrolactones by the Ugi Multicomponent Condensation Reaction
이덕형
Tet. Lett., 199806
53
Comparison of Inodilator Effect of Higenamine, YS49, YS51, Tetrahydroisoquinoline Analogs, and Dobutamine in the Rat
이덕형
The Korean Journal of Physiology & Pharmacology, 199806
54
Pharmacological Characterization of Synthetic Tetrahydroisoquinoline Alkaloids, YS 51 and YS 55, on the Cardiovascular System
이덕형
The Korean Journal of Physiology & Pharmacology, 199806
55
Enantioselective Synthesis of the C1-C28 Portion of the Cytotoxic Natural Product, Amphidinolide B1
이덕형
Tet. Lett., 199706
56
Convenient Routes to Symmetrical Benzils and Chiral 1,2-Diaryl-1,2-diaminoethanes, Useful Controllers and Probes for Enantioselective Synthesis
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Tet. Asymmetry, 199506
57
First Example of a Highly Enantioselective Catalytic Diels-Alder Reaction of an Achiral C₂v-Symmetric Dienophile and an Achiral Diene
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J. Am. Chem. Soc., 199411
58
The E/Z Geometry of the Enolate Component Determines Face Selectivity of the Aldehyde Component in Chiral Diazaborolidine-directed Enantioselective Aldol Coupling
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Tet. Lett., 199311
59
An Enantioselective Synthesis of(2S,3S)-and(2R,3S)-3-Hydroxyleucine
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Tet. Lett., 199211
60
Highly Enantioselective and Diastereoselective Ireland-Claisen Rearrangement of Achiral Allylic Esters