Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ok Kyoung, Choi"'
Publikováno v:
Pharmaceuticals, Vol 15, Iss 1, p 64 (2022)
A series of (S)-3-(1-aminoethyl)-8-pyrimidinyl-2-phenylisoquinoline-1(2H)-ones 3a–3k was synthesized in 40–98% yield through Suzuki–Miyaura coupling using Pd(PPh3)2Cl2, Sphos, and K2CO3 in THF/H2O mixed solvent. All newly synthesized compounds
Externí odkaz:
https://doaj.org/article/eda4321930654f728106dafceaf77beb
Publikováno v:
Pharmaceuticals
A series of (S)-3-(1-aminoethyl)-8-pyrimidinyl-2-phenylisoquinoline-1(2H)-ones 3a–3k was synthesized in 40–98% yield through Suzuki–Miyaura coupling using Pd(PPh3)2Cl2, Sphos, and K2CO3 in THF/H2O mixed solvent. All newly synthesized compounds
Autor:
Ok Kyoung Choi, Byung Tae Cho
Publikováno v:
Tetrahedron: Asymmetry. 12:903-907
A facile synthesis of (1 S ,2 R )-indene oxide with >99% e.e. and (1 S ,2 S )- trans -2-bromo-1-indanol with 87% e.e. has been established by employing CBS-oxazaborolidine-catalyzed asymmetric borane reduction of 2- p -toluenesulfonyloxy-1-indanone u
Autor:
Ok Kyoung Choi, Byung Tae Cho
Publikováno v:
ChemInform. 33
Autor:
Ok Kyoung Choi, Byung Tae Cho
Publikováno v:
ChemInform. 33
and Ok Kyoung ChoiDepartment of Chemistry, Hallym University, Chunchon, Kangwondo 200-702, KoreaReceived July 18, 2001Keywords : (−)-B-Chlorodiisopinocampheylborane, (1S,2R)-1,2-Indene oxide, (1S,2R)-1-Amino-2-indanol,(1S,2R)-2-Amino-1-indanol, Asy
Publikováno v:
ChemInform. 35
In recent years, manychemical and biological methods for the synthesis ofoptically active epoxides, such as asymmetric epoxidation ofolefins, resolution of racemic epoxides and indirect chemicaltransformation, have been reported. However, the directa
Publikováno v:
Biotechnology letters. 25(1)
Ethanol, added as a de-emulsifier to separate oil and biocatalyst (or bacterial cells) from a three-phase (oil/biocatalyst/aqueous phase) emulsion, formed in diesel biodesulfurization employing Gordonia nitida, improved oil recovery by centrifugation
Autor:
Ok Kyoung Choi, Byung Tae Cho
Publikováno v:
ChemInform. 32
Publikováno v:
ChemInform. 33:94-94
A simple and efficient synthesis of chiral β-hydroxy p -tolylsulfides with high enantiomeric purity by CBS-oxazaborolidine-catalyzed asymmetric borane reduction of β-keto p -tolylsulfides using N -ethyl- N -isopropylaniline–borane complex as the
Autor:
Byungill Choi, Yun-Kyung Cho, Kyoung-Soo Lim, Seung-Jea Takh, Ok Kyoung Choi, Han Soo Kim, Won Kim, Joon-Han Shin
Publikováno v:
Korean Circulation Journal. 28:863
Background:Previous studies have indicated adenosine triphosphate (ATP) is as potent coronary vasodillator as adenosine (A). We designed this study to compare the vasomotion of coronary artery (CA)between the infusion of ATP and that of A (1). Method