Facile synthesis of stable isotope-labeled antibacterial agent RWJ-416457 and its metaboliteRONGHUI LIN; WEANER, Larry E.Journal of labelled compounds & radiopharmaceuticals. 2012, Vol 55, Num 7-8, pp 296-299, issn 0362-4803, 4 p.Article

Carbon-carbon double bond formation between α-haloketones and aldehydes promoted by samarium triiodideYONGPING YU; RONGHUI LIN; YONGMIN ZHANG et al.Tetrahedron letters. 1993, Vol 34, Num 28, issn 0040-4039, 4425, 4547-4550 [5 p.]Article

Rapid and efficient synthesis of stable isotope labeled [¹³C₄, D₄]-5-(hydroxymethyl)thiazole : versatile building block for biologically interesting compoundsRONGHUI LIN; SALTER, Rhys; YONG GONG et al.Journal of labelled compounds & radiopharmaceuticals. 2009, Vol 52, Num 3-4, pp 110-113, issn 0362-4803, 4 p.Article

Phenolic resins modified by nanocopper particles and their service performancesRONGHUI LIN; LIANG FANG; XINPING LI et al.Polymer-plastics technology and engineering (Softcover ed). 2006, Vol 45, Num 10-12, pp 1243-1249, issn 0360-2559, 7 p.Article

Synthesis and properties of novel phenolic resins modified with nanosized copper particlesRONGHUI LIN; LIANG FANG; XINPING LI et al.Polymer international. 2006, Vol 55, Num 11, pp 1249-1253, issn 0959-8103, 5 p.Article

Synthesis and evaluation of N-acyl sulfonamides as potential prodrugs of cyclin-dependent kinase inhibitor JNJ-7706621SHENLIN HUANG; CONNOLLY, Peter J; RONGHUI LIN et al.Bioorganic & medicinal chemistry letters (Print). 2006, Vol 16, Num 14, pp 3639-3641, issn 0960-894X, 3 p.Article

Design, synthesis, and evaluation of 3,4-disubstituted pyrazole analogues as anti-tumor CDK inhibitorsRONGHUI LIN; CHIU, George; YANG YU et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 16, pp 4557-4561, issn 0960-894X, 5 p.Article

Synthesis and evaluation of 2,7-diamino-thiazolo[4,5-d] pyrimidine analogues as anti-tumor epidermal growth factor receptor (EGFR) tyrosine kinase inhibitorsRONGHUI LIN; JOHNSON, Sigmond G; FUENTES-PESQUERA, Angel R et al.Bioorganic & medicinal chemistry letters (Print). 2009, Vol 19, Num 8, pp 2333-2337, issn 0960-894X, 5 p.Article

Synthesis of 3 -(1H -benzimidazol -2 -yl ) -5 -isoquinolin-4 -ylpyrazolo[1,2 -b]pyridine, a potent cyclin dependent kinase 1 (CDK1) inhibitorSHENLIN HUANG; RONGHUI LIN; YANG YU et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 5, pp 1243-1245, issn 0960-894X, 3 p.Article

4-Aryl-5-cyano-2-aminopyrimidines as VEGF-R2 inhibitors: Synthesis and biological evaluationHUGHES, Terry V; EMANUEL, Stuart L; MIDDLETON, Steven A et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 12, pp 3266-3270, issn 0960-894X, 5 p.Article

3-acyl-2,6-diaminopyridines as cyclin-dependent kinase inhibitors : Synthesis and biological evaluationRONGHUI LIN; YANHUA LU; PANDEY, Niranjan et al.Bioorganic & medicinal chemistry letters (Print). 2005, Vol 15, Num 9, pp 2221-2224, issn 0960-894X, 4 p.Article

The in vitro and in vivo effects of JNJ-7706621 : A dual inhibitor of cyclin-dependent kinases and aurora kinasesEMANUEL, Stuart; RUGG, Catherine A; JOLLIFFE, Linda et al.Cancer research (Baltimore). 2005, Vol 65, Num 19, pp 9038-9046, issn 0008-5472, 9 p.Article

Synthesis and evaluation of pyrazolo[3,4-b]pyridine CDK1 inhibitors as anti-tumor agentsRONGHUI LIN; CONNOLLY, Peter J; GRUNINGER, Robert H et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 15, pp 4297-4302, issn 0960-894X, 6 p.Article

1-acyl-1H-[1,2,4]triazole-3,5-diamine analogues as novel and potent anticancer cyclin-dependent kinase inhibitors : Synthesis and evaluation of biological activities : 2005 American Chemical Society Award for Computers in Chemical and Pharmaceutical ResearchRONGHUI LIN; CONNOLLY, Peter J; MIDDLETON, Steven A et al.Journal of medicinal chemistry (Print). 2005, Vol 48, Num 13, pp 4208-4211, issn 0022-2623, 4 p.Article