Sung‐Gon Kim

Juntendo University Nerima Hospital

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Kyo Han Ahn

Pohang University of Science and Technology

Muneaki Ishijima

Juntendo University

Hiroshi Ikeda

Kyushu Dental University

Hisashi Kurosawa

Tokyo Metropolitan Geriatric Hospital

Masahiko Nozawa

University of Tokyo Health Sciences

Jin-Seong Lee

Daejeon Woori Hospital

Junyang Jung

Kyung Hee University

Woo‐Young Jung

Pusan National University Yangsan Hospital

Hyeon‐Kyeong Kim

Pusan National University

Yuko Sakamoto

Juntendo University Nerima Hospital

Cooperative Institutions

Sartorius (United States)

113

Juntendo University

Kyonggi University

Pusan National University

Seoul National University

Juntendo University Hospital

Pohang University of Science and Technology

Pusan National University Yangsan Hospital

Yonsei University

Korea Advanced Institute of Science and Technology

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CCDC 2308062: Experimental Crystal Structure Determination

The Cambridge Structural Database (2023)

Ji Won Han Yoseop Kim Sung‐Gon Kim

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

10.5517/ccdc.csd.cc2hgqmb

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CCDC 2207106: Experimental Crystal Structure Determination

The Cambridge Structural Database (2023)

Jaeeun No Young Jae Yun Sung‐Gon Kim

10.5517/ccdc.csd.cc2d2nz4

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CCDC 983605: Experimental Crystal Structure Determination

The Cambridge Structural Database (2014)

Shinae Kim Ki‐Tae Kang Sung‐Gon Kim

Crystal (programming language)

10.5517/cc120j6t

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CCDC 640688: Experimental Crystal Structure Determination

The Cambridge Structural Database (2007)

Sung‐Gon Kim Sang‐Ho Lee Tae-Ho Park

10.5517/ccphpc6

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ChemInform Abstract: Selective Recognition of NH₄⁺ over K⁺ with Tripodal Oxazoline Receptors.

ChemInform (2000)

Kyo Han Ahn Sung‐Gon Kim Junyang Jung Kyung‐Hyun Kim Jaheon Kim

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Oxazoline

10.1002/chin.200023127

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Concise Total Synthesis of (+)-Disparlure and its trans-Isomer Using Asymmetric Organocatalysis

Synthesis (2009)

Sung‐Gon Kim

The efficient enantioselective synthesis of (+)-disparlure and its trans-isomer is described. This approach involves tandem asymmetric organocatalytic α-aminoxylation-allylation of an aldehyde and olefin cross metathesis using Grubbs' catalyst as key steps.

Tandem

Olefin Metathesis

10.1055/s-0029-1216855

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Citations (31)

Asymmetric One‐Pot Synthesis of 1,4‐Dihydroquinolines via an Organocatalytic Aza‐Michael/Michael Cascade Strategy

Advanced Synthesis & Catalysis (2015)

Yona Lee Seungpyeong Heo Sung‐Gon Kim

Abstract A synthetic method for the construction of fully substituted enantioenriched 1,4‐dihydroquinolines using an organocatalytic aza‐Michael/Michael cascade reaction has been developed. The asymmetric reaction of 2‐(tosylamino)phenyl α,β‐unsaturated ketones with alkynyl aldehydes, promoted by diphenylprolinol O ‐TMS ether as an organocatalyst, generated chiral 1,4‐dihydroquinolines in good to high yields with excellent enantioselectivities (up to 97 % ee ). magnified image

Michael reaction

Cascade reaction

10.1002/adsc.201401176

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Citations (34)

Gender Differences in Alcohol Metabolizing Hepatic Enzyme Genotypes in Korean Patients with Alcohol Dependence

Addiction Genetics (2013)

Jin-Seong Lee Sung‐Gon Kim Sae-Heon Jang Won‐Tan Byun In-Bok Hwang

Abstract There are a number of epidemiological studies concerning the gender differences in the genetic etiology of alcohol dependence (AD), with ADH2 and ALDH2 being strong candidates. The purpose of this study was to investigate gender differences in frequencies of ADH2 and ALDH2 genotypes in AD patients and in a normal control (NC) group of Koreans. Study subjects consisted of 228 AD patients (180 males, 48 females) and 138 NC (79 males, 59 females). For both male and female subjects, the frequency of the ADH2*1/1 genotype was significantly higher in AD patients compared to the NC group. However, the effect size of the ADH2*1/1 genotype on AD was much larger in females than in males. Furthermore, the ALDH2*1/1 genotype was positively associated with AD in male subjects but negatively associated with AD in female patients. Interestingly, AD in males was primarily determined by ALDH2 enzyme activity (92%), whereas female AD was primarily determined by ADH2 enzyme activity (60.4%). These results suggest that risk for the development of AD in males is mainly associated with the ALDH2*1/1 genotype, while in female patients, the ADH2*1/1 genotype was more highly associated with risk of AD. Overall, it is evident that gender differences associated with genetic risks for AD are present.

ALDH2

Etiology

Alcohol intake

10.2478/addge-2013-0001

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Citations (1)

CCDC 197024: Experimental Crystal Structure Determination

The Cambridge Structural Database (2005)

Jonothan Austin Sung‐Gon Kim Christopher J. Sinz Wen‐Jing Xiao David W. C. MacMillan

Crystal (programming language)

10.5517/cc6m0mf

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Front Cover Picture: HFIP‐Mediated Decarboxylative [4+3]‐Annulation of Azaoxyallyl Cations with Isatoic Anhydride (Adv. Synth. Catal. 17/2020)

Advanced Synthesis & Catalysis (2020)

Eunjin Kim Chang Yoon Lee Sung‐Gon Kim

The front cover picture, provided by Sung-Gon Kim and his co-workers, illustrates an efficient [4+3]-annulation reaction between in situ generated azaoxyallyl cations and isatoic anhydride to afford seven-membered 1,4-benzodiazepinediones. This annulation involves the cascade reaction of decarboxylative addition of hexafluoroisopropanol (HFIP) to isatoic anhydride, addition to the azaoxyallyl cation generated from α-halohydroxamate, and intramolecular substitution to yield 1,4-benzodiazepinediones. Details of this work can be found in the full paper on pages 3594–3603 (E. Kim, C. Y. Lee, S.-G. Kim, Adv. Synth. Catal. 2020, 362, 3594–3603; DOI: 10.1002/adsc.202000439).

Annulation

Front cover

10.1002/adsc.202000800

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