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Yinhua Huang

Researcher at National University of Singapore

Publications -  10
Citations -  354

Yinhua Huang is an academic researcher from National University of Singapore. The author has contributed to research in topics: Enantioselective synthesis & Catalysis. The author has an hindex of 5, co-authored 10 publications receiving 299 citations. Previous affiliations of Yinhua Huang include Agency for Science, Technology and Research & Nanyang Technological University.

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Journal ArticleDOI

Asymmetric Synthesis of Triarylmethanes by Rhodium-Catalyzed Enantioselective Arylation of Diarylmethylamines with Arylboroxines.

TL;DR: The reaction of racemic diarylmethylamines with arylboroxines in the presence of a chiral diene-rhodium catalyst gave high yields of chiral triarylmethanes with high enantioselectivity.
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Asymmetric Synthesis of P-Stereogenic Diarylphosphinites by Palladium-Catalyzed Enantioselective Addition of Diarylphosphines to Benzoquinones

TL;DR: The reaction of phenyl(2,4,6-trimethylphenyl)phosphine with a substituted benzoquinone in the presence of a chiral phosphapalladacycle complex as a catalyst and triethylamine in chloroform proceeded in a new type of addition manner to give a high yield of a 4-hydroxyphenyl phenyl-phosphinite with 98% enantioselectivity.
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Asymmetric Conjugate Alkynylation of Cyclic α,β‐Unsaturated Carbonyl Compounds with a Chiral Diene Rhodium Catalyst

TL;DR: Asymmetric conjugate alkynylation of cyclic α,β-unsaturated carbonyl compounds (ketones, esters, and amides) was realized by use of diphenyl[(triisopropylsilyl)ethynyl]methanol as an alkynyating reagent in the presence of a rhodium catalyst coordinated with a new chiral diene ligand.
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Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles

TL;DR: An enantioselective Michael addition reaction of diphenylphosphine to substituted alkenylisoxazole has been developed, providing a hitherto unavailable direct access to a library of chiral tertiary phosphine-functionalized isoxazoles.
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Palladacycle catalyzed asymmetric P-H addition of diarylphosphines to N-enoyl phthalimides.

TL;DR: The first asymmetric phospha-Michael addition of diarylphosphines to N-enoyl phthalimides has been developed in the presence of a chiral palladacycle catalyst and a library of free chiral tertiary phosphine adducts were directly obtained with excellent yields and enantioselectivities.