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Scopus Author ID: 7409758560

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South Korea

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Employment (5)

Seoul National University College of Pharmacy: Seoul, KR

2013-09-01 to present | Professor Emeritus
Employment
Source: Self-asserted source
Deukjoon Kim

Seoul National University College of Pharmacy: Seoul, KR

1993-04-01 to 2013-08-31 | Professor
Employment
Source: Self-asserted source
Deukjoon Kim

Seoul National University College of Pharmacy: Seoul, KR

1987-10-01 to 1993-03-31 | Associate Professor
Employment
Source: Self-asserted source
Deukjoon Kim

Seoul National University College of Pharmacy: Seoul, KR

1983-08-04 to 1987-09-30 | Assistant Professor
Employment
Source: Self-asserted source
Deukjoon Kim

Korea Institute of Science and Technology: Seoul, KR

1981-09-01 to 1983-08-03 | Senior Research Associate
Employment
Source: Self-asserted source
Deukjoon Kim

Education and qualifications (3)

Columbia University: New York, NY, US

1977-09 to 1981-08 | Postdoctoral Research Fellow (Department of Chemistry)
Education
Source: Self-asserted source
Deukjoon Kim

Fordham University: New York, NY, US

1973-09 to 1979-02 | Ph.D. (Department of Chemstry)
Education
Source: Self-asserted source
Deukjoon Kim

College of Pharmacy, Seoul National University: Seoul, KR

1966-03 to 1970-02 | B.S.
Education
Source: Self-asserted source
Deukjoon Kim

Funding (1)

Ministry of Science, ICT and Future Planning

Grant
NRF (Seoul, KR)
Part of GRANT_NUMBER: 2007-0056817
Source: Self-asserted source
Deukjoon Kim

Works (50 of 51)

Items per page:
Page 1 of 2

Highly Stereodivergent Construction of a C<sub>2</sub>-Symmetric <i>cis</i>,<i>cis</i>- and <i>trans</i>,<i>trans</i>-2,6-Dioxabicyclo[3.3.0]octane Framework by Double Intramolecular Amide Enolate Alkylation: Total Synthesis of (+)-Laurenidificin and (+)-Aplysiallene

Organic Letters
2022-12-09 | Journal article | Author
DOI: 10.1021/acs.orglett.2c03494
Part of ISSN: 1523-7060
Part of ISSN: 1523-7052
Contributors: Iljin Shin; Hongjun Jang; Soo Yeon Kwak; Youngjik Park; Dongjoo Lee; Hyoungsu Kim; Deukjoon Kim
Source: Self-asserted source
Deukjoon Kim

Highly Stereoselective Asymmetric Total Synthesis of (−)-Jimenezin via Sequential Intramolecular Amide Enolate Alkylation

Organic Letters
2022-03-04 | Journal article
DOI: 10.1021/acs.orglett.2c00196
Part of ISSN: 1523-7060
Part of ISSN: 1523-7052
Contributors: Deukjoon Kim
Source: Self-asserted source
Deukjoon Kim

Asymmetric Total Synthesis and Determination of the Absolute Configuration of (+)-Srilankenyne via Sequence-Sensitive Halogenations Guided by Conformational Analysis

Organic Letters
2021-02-19 | Journal article
DOI: 10.1021/acs.orglett.0c04303
Part of ISSN: 1523-7060
Part of ISSN: 1523-7052
Contributors: Deukjoon Kim
Source: Self-asserted source
Deukjoon Kim

Structure Determination of a Chloroenyne from Laurencia majuscula Using Computational Methods and Total Synthesis

Journal of Organic Chemistry
2019 | Journal article
DOI: 10.1021/acs.joc.8b02975
Source: Self-asserted source
Deukjoon Kim

Asymmetric Total Syntheses and Structure Confirmation of Chlorofucins and Bromofucins

Chemistry - A European Journal
2018 | Journal article
DOI: 10.1002/chem.201704564
EID:

2-s2.0-85040964892
Contributors: Kim, B.; Sohn, T.-I.; Kim, D.; Paton, R.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Stereoselective Protection-Free Asymmetric Total Synthesis of (+)-Chamuvarinin, a Potent Anticancer and Antitrypanosomal Agent: Substrate-Controlled Construction of the Adjacently Linked Oxatricyclic Core by Internal Alkylation

Organic Letters
2018 | Journal article
DOI: 10.1021/acs.orglett.8b02706
EID:

2-s2.0-85054769022
Contributors: Samala, M.; Lu, T.N.; Mandava, S.; Hwang, J.; Bogonda, G.; Kim, D.; Park, H.; Kim, D.; Lee, J.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Construction of 6,10-syn- and -anti-2,5-Dioxabicyclo[2.2.1]heptane Skeletons via Oxonium Ion Formation/Fragmentation: Prediction of Structure of (E)-Ocellenyne by NMR Calculation

Organic Letters
2017 | Journal article
DOI: 10.1021/acs.orglett.7b03226
EID:

2-s2.0-85034585483
Contributors: Jeong, D.; Sohn, T.-I.; Kim, J.Y.; Kim, G.; Kim, D.; Paton, R.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Stereoselective substrate-controlled asymmetric syntheses of both 2,5-cis- and 2,5-trans-tetrahydrofuranoid oxylipids: Stereodivergent intramolecular amide enolate alkylation

Angewandte Chemie - International Edition
2016 | Journal article
DOI: 10.1002/anie.201600637
EID:

2-s2.0-84969645924
Contributors: Jang, H.; Shin, I.; Lee, D.; Kim, H.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Substrate-Controlled Asymmetric Total Syntheses of Microcladallenes A, B, and C Based on the Proposed Structures

Chemistry - A European Journal
2015 | Journal article
DOI: 10.1002/chem.201502592
EID:

2-s2.0-84945472366
Contributors: Sohn, T.-I.; Kim, D.; Paton, R.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Asymmetric total synthesis of (+)-bermudenynol, a C<inf>15</inf>laurencia metabolite with a vinyl chloride containing oxocene skeleton, through intramolecular amide enolate alkylation

Angewandte Chemie - International Edition
2014 | Journal article
DOI: 10.1002/anie.201308077
EID:

2-s2.0-84890929596
Contributors: Kim, G.; Sohn, T.-I.; Kim, D.; Paton, R.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Intramolecular enolate alkylation: From steroids through cladiellins to isolaurallene

Synlett
2014 | Journal article
DOI: 10.1055/s-0033-1340050
EID:

2-s2.0-84890788299
Contributors: Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Concise substrate-controlled asymmetric total syntheses of dioxabicyclic marine natural products with 2,10-dioxabicyclo-[7.3.0]dodecene and 2,9-dioxabicyclo[6.3.0]undecene skeletons

Journal of the American Chemical Society
2012 | Journal article
DOI: 10.1021/ja310249u
EID:

2-s2.0-84870862154
Contributors: Kim, M.J.; Sohn, T.-I.; Kim, D.; Paton, R.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Total synthesis and structure confirmation of elatenyne: Success of computational methods for NMR prediction with highly flexible diastereomers

Journal of the American Chemical Society
2012 | Journal article
DOI: 10.1021/ja304554e
EID:

2-s2.0-84863888143
Contributors: Dyson, B.S.; Burton, J.W.; Sohn, T.-I.; Kim, B.; Bae, H.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A stereoselective total synthesis of (±)-tormesol

Tetrahedron
2011 | Journal article
DOI: 10.1016/j.tet.2011.09.022
EID:

2-s2.0-81255134400
Contributors: Kim, H.; Bae, H.; Kim, S.; Kim, D.; Lee, D.; Paton, R.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Asymmetric total synthesis of trilobacin via organoselenium-mediated oxonium ion formation/SiO<inf>2</inf>-Promoted fragmentation

Journal of the American Chemical Society
2010 | Journal article
DOI: 10.1021/ja106116v
EID:

2-s2.0-77956255066
Contributors: Sohn, T.-I.; Kim, M.J.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Concise substrate-controlled asymmetric total synthesis of (+)-3-(Z)-dihydrorhodophytin

Heterocycles
2010 | Journal article
DOI: 10.3987/COM-10-S(E)76
EID:

2-s2.0-79952770933
Contributors: Kim, B.; Sohn, T.I.; Kim, S.; Kim, D.; Lee, J.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Substrate-controlled asymmetric total synthesis and structure revision of (+)-itomanallene a

Angewandte Chemie - International Edition
2010 | Journal article
DOI: 10.1002/anie.200905826
EID:

2-s2.0-74849130230
Contributors: Jeong, W.; Kim, M.J.; Kim, H.; Kim, S.; Kim, D.; Shin, K.J.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A general strategy for construction of both 2,6-cis- and 2,6-trans-disubstituted tetrahydropyrans: Substrate-controlled asymmetric total synthesis of (+)-scanlonenyne

Angewandte Chemie - International Edition
2008 | Journal article
DOI: 10.1002/anie.200705663
EID:

2-s2.0-47049118956
Contributors: Lee, H.; Kim, K.W.; Park, J.; Kim, H.; Kim, S.; Kim, D.; Hu, X.; Yang, W.; Hong, J.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Biomimetic asymmetric total synthesis of (-)-laurefucin via an organoselenium-mediated intramolecular hydroxyetherification

Journal of the American Chemical Society
2008 | Journal article
DOI: 10.1021/ja806304s
EID:

2-s2.0-57549083399
Contributors: Kim, B.; Lee, M.; Mi, J.K.; Lee, H.; Kim, S.; Kim, D.; Koh, M.; Seung, B.P.; Kye, J.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Asymmetric total syntheses of (+)-3-(Z)-laureatin and (+)-3-(Z)- isolaureatin by "lone pair-lone pair interaction-controlled" isomerization

Journal of the American Chemical Society
2007 | Journal article
DOI: 10.1021/ja068346i
EID:

2-s2.0-33847637959
Contributors: Kim, H.; Lee, H.; Lee, D.; Kim, S.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Substrate-controlled asymmetric total synthesis of (+)-microcladallene B with a bromination strategy based on a nucleophile-assisting leaving group

Angewandte Chemie - International Edition
2007 | Journal article
DOI: 10.1002/anie.200700854
EID:

2-s2.0-34347223272
Contributors: Park, J.; Kim, B.; Kim, H.; Kim, S.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Substrate-controlled formal synthesis of (+)-laurenyne by a chemoselective chelation-controlled alkylation strategy

Heterocycles
2007 | Journal article
EID:

2-s2.0-40749092903
Contributors: Kim, B.; Cheon, G.; Park, J.; Lee, H.; Kim, H.; Kim, S.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A general strategy for synthesis of both (6Z)- and (6E)-cladiellin diterpenes: Total syntheses of (-)-cladiella-6,11-dien-3-ol, (+)-polyanthellin A, (-)-cladiell-11-ene-3,6,7-triol, and (-)-deacetoxyalcyonin acetate

Journal of the American Chemical Society
2006 | Journal article
DOI: 10.1021/ja065782w
EID:

2-s2.0-33845462422
Contributors: Kim, H.; Lee, H.; Kim, J.; Kim, S.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

An approach to cyclic -amino acids by a novel hetero diels-alder/intramolecular hydantoin enolate alkylation strategy: An approach to halichlorine

Heterocycles
2006 | Journal article
DOI: 10.3987/COM-06-S(W)43
EID:

2-s2.0-33947674836
Contributors: Kim, H.; Seo, J.H.; Shin, K.J.; Kim, D.J.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Highly stereoselective and efficient total synthesis of (+)-laurencin

Organic Letters
2005 | Journal article
DOI: 10.1021/ol047877d
EID:

2-s2.0-12344258149
Contributors: Baek, S.; Jo, H.; Kim, H.; Kim, H.; Kim, S.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Novel "protecting group-dependent" alkylation-RCM strategy to medium-sized oxacycles: First total synthesis of (-)-isoprelaurefucin

Journal of Organic Chemistry
2005 | Journal article
DOI: 10.1021/jo050974f
EID:

2-s2.0-27444447985
Contributors: Lee, H.; Kim, H.; Yoon, T.; Kim, B.; Kim, S.; Kim, H.-D.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

5-Demethoxyfumagillol, a potent angiogenesis inhibitor isolated from Aspergillus fumigatus

Chemical and Pharmaceutical Bulletin
2004 | Journal article
DOI: 10.1248/cpb.52.447
EID:

2-s2.0-4444263991
Contributors: Kim, D.; Min, J.; Ahn, S.K.; Lee, H.W.; Choi, N.S.; Moon, S.K.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Construction of eight-membered ether rings by olefin geometry-dependent internal alkylation: First asymmetric total syntheses of (+)-3-(E)- and (+)-3-(Z)-pinnatifidenyne

Journal of the American Chemical Society
2003 | Journal article
DOI: 10.1021/ja035538u
EID:

2-s2.0-0042931243
Contributors: Kim, H.; Choi, W.J.; Jung, J.; Kim, S.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Efficient construction of bicyclic systems by an internal S<inf>N</inf>2′ enolate alkylation/ring-closing metathesis (RCM) strategy: A concise synthesis of the trans-hydrindane nucleus

Tetrahedron Letters
2003 | Journal article
DOI: 10.1016/S0040-4039(03)01780-5
EID:

2-s2.0-0041657321
Contributors: Jo, H.; Lee, J.; Kim, H.; Kim, S.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Total synthesis and determination of the absolute configuration of (+)-neoisoprelaurefucin

Tetrahedron Letters
2003 | Journal article
DOI: 10.1016/S0040-4039(03)01667-8
EID:

2-s2.0-0041624518
Contributors: Lee, H.; Kim, H.; Baek, S.; Kim, S.; Kim, D.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Asymmetric total synthesis of (+)-brefeldin A from (S)-lactate by triple chirality transfer process and nitrile oxide cycloaddition

Journal of Organic Chemistry
2002 | Journal article
DOI: 10.1021/jo010743i
EID:

2-s2.0-0037039925
Contributors: Kim, D.; Lee, J.; Phil, J.S.; Joong, I.L.; Jo, H.; Kim, S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Role of conformational effects on the regioselectivity of macrocyclic INOC reactions: Two new asymmetric total syntheses of (+)-brefeldin A

Journal of Organic Chemistry
2002 | Journal article
DOI: 10.1021/jo010744a
EID:

2-s2.0-0037039952
Contributors: Kim, D.; Lee, J.; Phil, J.S.; Joong, I.L.; Doi, T.; Kim, S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Stereoselective synthesis of (±)-β-elemene by a doubly diastereodifferentiating internal alkylation: A remarkable difference in the rate of enolization between syn and anti esters

Tetrahedron
2001 | Journal article
DOI: 10.1016/S0040-4020(00)01130-3
EID:

2-s2.0-0035843381
Contributors: Kim, D.; Lee, J.; Chang, J.; Kim, S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Construction of the tricyclo[5.3.1.0<sup>1,5</sup>]undecane system by a novel tandem pinacol rearrangement-ene strategy: A formal total synthesis of (±)-perhydrohistrionicotoxin

Journal of Organic Chemistry
2000 | Journal article
DOI: 10.1021/jo000136f
EID:

2-s2.0-0342646940
Contributors: Kim, D.; Shim, P.J.; Lee, J.; Park, C.W.; Hong, S.W.; Kim, S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A stereoselective total synthesis of (±)-oppositol by a doubly diastereoselective intramolecular ester enolate alkylation

Tetrahedron Letters
1997 | Journal article
DOI: 10.1016/S0040-4039(96)02313-1
EID:

2-s2.0-0031012520
Contributors: Kim, D.; Kim, I.H.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

An asymmetric total synthesis of (-)-fumagillol

Tetrahedron Letters
1997 | Journal article
DOI: 10.1016/S0040-4039(97)00925-8
EID:

2-s2.0-0030986585
Contributors: Kim, D.; Ahn, S.K.; Bae, H.; Choi, W.J.; Kim, H.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Construction of the tricyclo[5.3.1.0<sup>1,5</sup>]undecane system by a tandem pinacol rearrangement-ene strategy: A formal synthesis of (±)-perhydrohistrionicotoxin

Chemical Communications
1997 | Journal article
DOI: 10.1039/a706193e
EID:

2-s2.0-0007322358
Contributors: Kim, D.; Hong, S.W.; Park, C.W.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

An asymmetric synthesis of (+)-isonitramine by 'triple allylic strain-controlled' intramolecular S<inf>N</inf>2' alkylation

Tetrahedron Letters
1996 | Journal article
DOI: 10.1016/0040-4039(96)00023-8
EID:

2-s2.0-0030001954
Contributors: Kim, D.; Choi, W.J.; Hong, J.Y.; Park II, Y.; Kim, Y.B.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A stereoselective route to a cyclopentanoid natural product synthon via intramolecular ester enolate alkyaltion

Archives of Pharmacal Research
1995 | Journal article
DOI: 10.1007/BF02976512
EID:

2-s2.0-0028863092
Contributors: Kim, D.; Shin, K.J.; Park, S.W.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A synthetic approach to (+)-brefeldin A

Tetrahedron Letters
1995 | Journal article
DOI: 10.1016/0040-4039(95)00915-Y
EID:

2-s2.0-0029010279
Contributors: Kim, D.; Lim, J.I.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A stereospecific synthesis of (±)-grandisol via an intramolecular lactone enolate alkylation: A remarkable regiodivergence in C- vs O-alkylation

Tetrahedron Letters
1994 | Journal article
DOI: 10.1016/0040-4039(94)88468-4
EID:

2-s2.0-0028109564
Contributors: Kim, D.; Kwak, Y.S.; Shin, K.J.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A total synthesis of (-)-reiswigin a via sequential claisen rearrangement-intramolecular ester enolate alkylation

Tetrahedron Letters
1994 | Journal article
DOI: 10.1016/0040-4039(94)80021-9
EID:

2-s2.0-0028091969
Contributors: Kim, D.; Shin, K.J.; Kim, I.Y.; Park, S.W.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A stereoselective synthesis of (±)-elemol via an intramolecular S<inf>N</inf>2′ ester enolate alkylation

Tetrahedron Letters
1993 | Journal article
DOI: 10.1016/0040-4039(93)88103-P
EID:

2-s2.0-0027482163
Contributors: Kim, D.; Lim, J.I.; Shin, K.J.; Kim, H.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A total synthesis of spirocyclic alkaloids via an intramolecular S<inf>N</inf>2′ lactam enolate alkylation

Tetrahedron Letters
1991 | Journal article
DOI: 10.1016/S0040-4039(00)74276-6
EID:

2-s2.0-0026071469
Contributors: Kim, D.; Sung Kim, H.; Yeol Yoo, J.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Stereoselective synthesis of a steroidal trans-hydrindanone synthon from (R)-limonene

Tetrahedron Letters
1991 | Journal article
DOI: 10.1016/0040-4039(91)80434-8
EID:

2-s2.0-0026061375
Contributors: Kim, D.; Lee, Y.K.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Stereoselective construction of steroidal trans-hydrindanes via intramolecular ester enolate alkylation[1,2]

Tetrahedron Letters
1990 | Journal article
DOI: 10.1016/S0040-4039(00)94490-3
EID:

2-s2.0-0025372270
Contributors: Deukjoon, K.; Sanghee, K.; Jae, J.L.; Hak, S.K.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Stereoselective synthesis of racemic fragranol by an intramolecular ester enolate alkylation

Journal of the Chemical Society, Perkin Transactions 1
1990 | Journal article
EID:

2-s2.0-37049079828
Contributors: Kim, D.; Lee, Y.K.; Jang, Y.M.; Kim, I.O.; Park, S.W.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Stereoselective ester enolate alkylation and hydroxylation at C-22 of a steroid side chain

Tetrahedron Letters
1989 | Journal article
DOI: 10.1016/S0040-4039(00)99524-8
EID:

2-s2.0-0007178581
Contributors: Kim, D.; Hee Han, G.; Kim, K.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

A stereoselective route to vicinally substituted cyclopentane- and cyclobutane-carboxylates

Journal of the Chemical Society, Chemical Communications
1988 | Journal article
DOI: 10.1039/C39880000760
EID:

2-s2.0-37049078138
Contributors: Kim, D.; Jang, Y.M.; Kim, I.O.; Park, S.W.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier

Stereoselective Construction of Functionalized cis- 1,2-Dialkylcyclohexanecarboxylates: A Novel Synthesis of (±)-Geijerone and γ-Elemene

Journal of Organic Chemistry
1987 | Journal article
DOI: 10.1021/jo00229a045
EID:

2-s2.0-0009719598
Contributors: Kim, D.; Kim, H.S.
Source: Self-asserted source
Deukjoon Kim via Scopus - Elsevier
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