Guoliang Lin

发表

Metal-free visible-light induced cross-dehydrogenative coupling of tertiary amines with diazo compounds.

Z. Mao, Lei Zhou, Tiebo Xiao, 2014, Organic letters.

Synthesis of 6-substituted phenanthridines by metal-free, visible-light induced aerobic oxidative cyclization of 2-isocyanobiphenyls with hydrazines

Z. Mao, Lei Zhou, Tiebo Xiao, 2014 .

C6-Substituted methanopyrrolidine β-amino acid: synthesis and characterization of oligomeric foldamers

Zilun Hu, F. A. Davis, Guoliang Lin, 2020 .

Novel selectfluor and deoxo-fluor-mediated rearrangements. New 5(6)-methyl and phenyl methanopyrrolidine alcohols and fluorides.

C. Debrosse, Keith P. Moore, Guoliang Lin, 2004, Organic letters.

Metal-free visible-light induced cross-dehydrogenative coupling of tertiary amines with diazo compounds.

Z. Mao, Lei Zhou, Tiebo Xiao, 2014, Organic letters.

Neighboring group participation in the additions of iodonium and bromonium ions to N-alkoxycarbonyl-2-azabicyclo[2.2.n]alk-5-enes (n = 1,2).

W. Guo, P. Carroll, C. Debrosse, 2008, The Journal of organic chemistry.

The rearrangement route to 2-azabicyclo[2.1.1]hexanes. Solvent and electrophile control of neighboring group participation.

S. Herzon, Guoliang Lin, P. Sonnet, 2003, The Journal of organic chemistry.

Second-chance rearrangement route to novel 5(6)-syn,anti-difunctional 2-azabicyclo[2.1.1]hexanes.

Guoliang Lin, P. Sonnet, G. Krow, 2003, Organic letters.

Complex-induced proximity effects. Temperature-dependent regiochemical diversity in lithiation-electrophilic substitution reactions of N-BOC-2-azabicyclo[2.1.1]hexane. 2,4- and 3,5-methanoprolines.

S. Herzon, Guoliang Lin, P. Sonnet, 2002, Organic letters.

Effect of lanthanide contraction on structures of lanthanide coordination polymers based on 5-aminoisophthalic acid and oxalate

Yuepeng Cai, Jing Chen, Xia Zhao, 2012 .

The rearrangement route to 3-CH(2)X-2-azabicyclo[2.1.1]hexanes. Substituent control of neighboring group participation.

Guoliang Lin, P. Sonnet, G. Krow, 2002, Organic letters.

Substituted 2-azabicyclo[2.1.1]hexanes as constrained proline analogues: implications for collagen stability.

R. Raines, I. Guzei, Cara L. Jenkins, 2004, The Journal of organic chemistry.

Discovery of novel cyanamide-based inhibitors of cathepsin C.

Baoguang Zhao, Neysa Nevins, R. Midgett, 2011, ACS medicinal chemistry letters.

The rearrangement route to 3-carboxy- and 3-hydroxymethyl-2-azabicyclo[2.1.1]hexanes: 3,5-methanoprolines.

Guoliang Lin, G. Krow, Fanglei Yu, 2005, The Journal of organic chemistry.

3,5-Disubstituted-indole-7-carboxamides as IKKβ Inhibitors: Optimization of Oral Activity via the C3 Substituent.

J. Boehm, P. Bamborough, Wei-Chang Fu, 2018, ACS medicinal chemistry letters.

Introduction of C(5/6) side chains onto 2-azabicyclo[2.1.1]hexanes via a 6-anti-bromo-5-anti-hydroxy derivative

Yufang, C. Debrosse, Guoliang Lin, 2012 .