Hongwu Yu - Publications
Affiliations: | 2001 | North Carolina State University, Raleigh, NC |
Year | Citation | Score | |||
---|---|---|---|---|---|
2010 | Tian H, She X, Yu H, Shu L, Shi Y. ChemInform Abstract: Designing New Chiral Ketone Catalysts. Asymmetric Epoxidation of cis-Olefins and Terminal Olefins. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200239054 | 0.326 | |||
2010 | Yu H, Wang B. ChemInform Abstract: Arylboronic Acid-Facilitated Selective Reduction of Aldehydes by Tributyltin Hydride. Cheminform. 32: no-no. DOI: 10.1002/chin.200151065 | 0.601 | |||
2010 | Yu H, Ballard CE, Wang B. ChemInform Abstract: A Highly Stereoselective Entry to α-Hydroxy Carboxylic Acids Using D-Fructose Diacetonide as a Chiral Auxiliary. Cheminform. 32: no-no. DOI: 10.1002/chin.200122066 | 0.716 | |||
2003 | Yu H, Ballard CE, Boyle PD, Wang B. An Inexpensive Carbohydrate Derivative Used as a Chiral Auxiliary in the Synthesis of α-Hydroxy Carboxylic Acids. Cheminform. 34. DOI: 10.1002/chin.200305074 | 0.715 | |||
2002 | Tian H, She X, Yu H, Shu L, Shi Y. Designing new chiral ketone catalysts. Asymmetric epoxidation of cis-olefins and terminal olefins. The Journal of Organic Chemistry. 67: 2435-46. PMID 11950285 DOI: 10.1021/Jo010838K | 0.323 | |||
2002 | Yu H, Ballard CE, Boyle PD, Wang B. An inexpensive carbohydrate derivative used as a chiral auxiliary in the synthesis of α-hydroxy carboxylic acids Tetrahedron. 58: 7663-7679. DOI: 10.1016/S0040-4020(02)00871-2 | 0.689 | |||
2001 | Yu H, Wang B. ARYLBORONIC ACID-FACILITATED SELECTIVE REDUCTION OF ALDEHYDES BY TRIBUTYLTIN HYDRIDE Synthetic Communications. 31: 2719-2725. DOI: 10.1081/Scc-100105400 | 0.625 | |||
2001 | Yu H, Ballard C, Wang B. A highly stereoselective entry to α-hydroxy carboxylic acids using d-fructose diacetonide as a chiral auxiliary Tetrahedron Letters. 42: 1835-1838. DOI: 10.1016/S0040-4039(01)00043-0 | 0.694 | |||
2001 | Tian H, She X, Shu L, Yu H, Shi Y. ChemInform Abstract: Highly Enantioselective Epoxidation of cis-Olefins by Chiral Dioxirane. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200113114 | 0.397 | |||
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