H
Ho Jung Kang
Researcher at Ohio State University
Publications - 9
Citations - 137
Ho Jung Kang is an academic researcher from Ohio State University. The author has contributed to research in topics: Total synthesis & Ring (chemistry). The author has an hindex of 5, co-authored 9 publications receiving 133 citations. Previous affiliations of Ho Jung Kang include University of Texas at Austin.
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Journal ArticleDOI
Synthetic studies on basmane diterpenes. Enantiospecific total synthesis of (+)-7,8-epoxy-2-basmen-6-one by Claisen ring expansion
Leo A. Paquette,Ho Jung Kang +1 more
TL;DR: In this paper, the authors compose du titre a partir d'5-isopropyl-2-methylcyclopent-1-ene carbaldehyde via the transposition Claisen d'un derive de cyclopenta pyrane en derive decyclopenta cyclooctene.
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Stereocontrolled Access to the Most Highly Condensed Pentalenolactone Antibiotic. from Cycloheptatriene to Pentalenolactone P Methyl Ester
TL;DR: The first total synthesis of cyclopropane-lactone was reported in this paper, where a regioselective chain-lengthening, oxadi-π-methane rearrangement, lactone ring construction by an intramolecular Michael reaction-oxidation sequence, and use of monomeric formaldehyde to introduce the final carbon atom.
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Claisen-based strategy for the de novo construction of basmane diterpenes. Enantiospecific synthesis of (+)-7,8-epoxy-2-basmen-6-one
Ho Jung Kang,Leo A. Paquette +1 more
TL;DR: In this article, the authors compose du titre a partir d'isopropyl 3 methyl-1 methylene-2 cyclopentaneacetaldehyde via une transposition.
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Stereocontrolled total synthesis of (.+-.)-pentalenolactone P methyl ester
Journal ArticleDOI
Constraining of small-ring cyclic ether triads by stereodefined spiroannulation to an inositol orthoformate platform. Solution- and gas-phase alkali metal binding affinities for three- to five-membered ring structural combinations.
Leo A. Paquette,Choon Sup Ra,Judith C. Gallucci,Ho Jung Kang,Naoki Ohmori,Mark P. Arrington,Wendi M. David,Jennifer S. Brodbelt +7 more
TL;DR: The structural features most conducive to complexation of the alkali metal ions Li(+, Na(+), and K(+) in a series of constrained inositol orthoformate derivatives have been probed in solution, in the solid state, and in the gas phase by electrospray ionization mass spectrometry.