Hoon Han

发表

Direct generation of acyclic polypropionate stereopolyads via double diastereo- and enantioselective iridium-catalyzed crotylation of 1,3-diols: beyond stepwise carbonyl addition in polyketide construction.

M. Krische, Xin Gao, Hoon Han, 2011, Journal of the American Chemical Society.

A facile access to N-sulfonylimidates and their synthetic utility for the transformation to amidines and amides.

Sukbok Chang, Hoon Han, S. Cho, 2006, Organic letters.

Highly efficient one-pot synthesis of N-sulfonylamidines by Cu-catalyzed three-component coupling of sulfonyl azide, alkyne, and amine.

Sukbok Chang, Hoon Han, Imhyuck Bae, 2005, Journal of the American Chemical Society.

Ruthenium-catalyzed Heck-type olefination and Suzuki coupling reactions: studies on the nature of catalytic species.

Sukbok Chang, Sangwon Ko, Soyoung Park, 2004, Journal of the American Chemical Society.

Copper-nitrenoid formation and transfer in catalytic olefin aziridination utilizing chelating 2-pyridylsulfonyl moieties.

Sukbok Chang, Sang Kyu Kim, Hoon Han, 2008, The Journal of organic chemistry.

Rh-catalyzed one-pot and practical transformation of aldoximes to amides.

Sukbok Chang, Soyoung Park, Hoon Han, 2003, Chemical communications.

Metal-Free Conversion of Carboxamides to Ureas Using Tertiary Amines and Iodosylmesitylene

Sukbok Chang, Hoon Han, 2010 .

Notable coordination effects of 2-pyridinesulfonamides leading to efficient aziridination and selective aziridine ring opening.

Sukbok Chang, Junseong Lee, Y. Do, 2004, Organic letters.

Cooperative Multi‐Catalyst Systems for One‐Pot Organic Transformations

Sukbok Chang, Ji Min Lee, Hoon Han, 2004 .

Cooperative multi-catalyst systems for one-pot organic transformations.

Hoon Han, Sukbok Chang, Ji Min Lee, 2004, Chemical Society reviews.

Diastereo- and enantioselective anti-alkoxyallylation employing allylic gem-dicarboxylates as allyl donors via iridium-catalyzed transfer hydrogenation.

M. Krische, Hoon Han, S. Han, 2010, Journal of the American Chemical Society.

Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-dimethylallene as the prenyl donor.

M. Krische, Hoon Han, S. Han, 2009, Journal of the American Chemical Society.

Halide ions as a highly efficient promoter in the Ru-catalyzed hydroesterification of alkenes and alkynes.

Sukbok Chang, Ji Min Lee, Hoon Han, 2006, Organic letters.

Ru-catalyzed hydroamidation of alkenes and cooperative aminocarboxylation procedure with chelating formamide.

Sukbok Chang, Sangwon Ko, Hoon Han, 2003, Organic letters.

All-carbon quaternary centers via ruthenium-catalyzed hydroxymethylation of 2-substituted butadienes mediated by formaldehyde: beyond hydroformylation.

T. Smejkal, M. Krische, B. Breit, 2009, Journal of the American Chemical Society.

A facile access to N-sulfonylimidates and their synthetic utility for the transformation to amidines and amides.

Sukbok Chang, Hoon Han, S. Cho, 2006, Organic letters.

Erratum: Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-Dimethylallene as the prenyl donor (Journal of the American Chemical Society (2009) 131 (6916-6917))

M. Krische, Hoon Han, S. Han, 2010 .

Direct ruthenium-catalyzed C-C coupling of ethanol: diene hydro-hydroxyethylation to form all-carbon quaternary centers.

M. Krische, Hoon Han, 2010, Organic letters.

Highly efficient iridium-catalyzed oxidation of organosilanes to silanols.

Sukbok Chang, Youngjun Lee, Phil Ho Lee, 2004, The Journal of organic chemistry.

Isotope-coded N-terminal sulfonation of peptides allows quantitative proteomic analysis with increased de novo peptide sequencing capability.

Sang-Won Lee, Hoon Han, Yong Ho Lee, 2004, Rapid communications in mass spectrometry : RCM.