G. Shi

发表

Synthesis and biological activities of novel aryl indole-2-carboxylic acid analogs as PPARγ partial agonists

J. Berger, T. Doebber, T. Akiyama, 2005 .

Synthesis and Biological Activities of Novel Aryl Indole‐2‐carboxylic Acid Analogues as PPARγ Partial Agonists.

J. Berger, T. Doebber, T. Akiyama, 2006 .

Palladium-Catalyzed Functionalization of Lactones via Their Cyclic Ketene Acetal Phosphates. Efficient New Synthetic Technology for the Construction of Medium and Large Cyclic Ethers

K. Nicolaou, Zhen Yang, J. Gunzner, 1997 .

Novel 2,3-dihydrobenzofuran-2-carboxylic acids: highly potent and subtype-selective PPARalpha agonists with potent hypolipidemic activity.

J. Berger, D. Moller, Gaochao Zhou, 2005, Journal of medicinal chemistry.

Ethyl 3-trifluoro-2-diazo-propionate as a potentially useful CF3-containing building block: preparation and [Rh(OAc)2]2-catalysed reaction with nitriles

Yuanyao Xu, G. Shi, 1989 .

2-(Acetoxymethyl)-1,1-difluoro-3-(trimethylsilyl)propene: Preparation and utility as a novel bifunctional reagent containing a CF2 group

G. Shi, Xian-hai Huang, 1996 .

A novel and versatile access to fluorinated carbo- and heterocyclic compounds employing electron-rich fluorodienes as cycloaddition components

M. Schlosser, G. Shi, 1993 .

The diels-alder approach to musk odor type arenes

S. Cottens, G. Shi, S. Shiba, 1992 .

Metalated fluoropyridines and fluoroquinolines as reactive intermediates: new ways for their regioselective generation

M. Schlosser, G. Shi, Sadahito Takagishi, 1994 .

Carbenoid entry into trifluoromethylated molecules: preparation of functionalized CF3-containing γ, δ -unsaturated carboxylic esters by rhodium-catalyzed reaction of ethyl 3,3,3-trifluoro-2-diazo-propionate with allylic sulfides and their further facile conversion to trifluoromethylated conjugated d

Yuanyao Xu, G. Shi, Ming‐Hua Xu, 1991 .

Versatile 2-Fluoroacrylic Building Blocks for the Synthesis of Fluorinated Heterocyclic Compounds

M. Schlosser, G. Shi, Qian Wang, 1996 .

NEW SYNTHETIC TECHNOLOGY FOR THE CONSTRUCTION OF 9-MEMBERED RING CYCLIC ETHERS. CONSTRUCTION OF THE EFGH RING SKELETON OF BREVETOXIN A

K. Nicolaou, Zhen Yang, J. Gunzner, 1997 .

Total Synthesis of Brevetoxin A: Part 3: Construction of GHIJ and BCDE Ring Systems

P. A. Wallace, M. Bunnage, K. Nicolaou, 1999 .

.delta.,.epsilon.-Unsaturated .beta.,.beta.-Difluoro-.alpha.-keto Esters: Novel Synthesis and Utility as Precursors of .beta.,.beta.-Difluoro-.alpha.-amino Acids

W. Cai, G. Shi, 1995 .

Rhodium-mediated insertion of CF3-substituted carbenoid into O-H: An efficient method for the synthesis of α-trifluoromethylated alkoxy- and aryloxyacetic acid derivatives

Z. Cao, W. Cai, G. Shi, 1995 .

Trifluoromethyl-substituted carbethoxy carbene as a novel CF~3-containing a^2 stbtgib equivalent for the preparation of 2-(trifluoromethyl)-4-oxo- carboxylic ester derivatives: highly functionalized synthetic building blocks bearing a CF~3 group

Yuanyao Xu, G. Shi, 1990 .

Regioselectivity in the addition of carbon nucleophiles to 1-fluoro and 1,1-difluoro π-allylpalladium complexes

G. Shi, Xuanping Huang, Fangfang Zhang, 1995 .

Total synthesis of brevetoxin A

K. Nicolaou, Zhen Yang, J. Gunzner, 1998, Nature.

Palladium-catalysed arylation and alkenylation of cis- trifluoroprop-1-enyl methyl ether. A novel entry into trifluoromethylated compounds.

F. Hong, G. Shi, Xian-hai Huang, 1996 .

Ethyl 2-Benzyloxy-3,3-difluoropropenoate as a novel synthon of β -fluoro-α-keto acid derivatives, preparation and reactions with nucleophiles

Z. Cao, G. Shi, 1995 .

TOTAL SYNTHESIS OF BREVETOXIN A : PART 2 : SECOND GENERATION STRATEGY AND CONSTRUCTION OF EFGH MODEL SYSTEM

P. A. Wallace, M. Bunnage, K. Nicolaou, 1999 .

Total Synthesis of Brevetoxin A: Part 4: Final Stages and Completion

K. Nicolaou, Zhen Yang, J. Gunzner, 1999 .

3,3-Difluoro-2-ethoxy-2-propenol: Preparation and utility as a novel synthon of α,α-difluoroketones

W. Cai, G. Shi, 1996 .

Design and synthesis of alpha-aryloxyphenylacetic acid derivatives: a novel class of PPARalpha/gamma dual agonists with potent antihyperglycemic and lipid modulating activity.

Y. Chao, J. Berger, D. Moller, 2005, Journal of medicinal chemistry.

Synthesis and biological activities of novel aryl indole-2-carboxylic acid analogs as PPARgamma partial agonists.

J. Berger, T. Doebber, T. Akiyama, 2005, Bioorganic & medicinal chemistry letters.

A convenient synthesis of 1,1-difluoroallenes from trifluoromethylketones via the shapiro reaction pathway

Yuanyao Xu, G. Shi, 1989 .

A Convenient Synthesis of 1,1-Difluoroallenes (IV) from Trifluoromethyl Ketones (I) via the Shapiro Reaction Pathway.

G. Shi, Y. Xu, 1989 .

Rhodium-catalysed decomposition of δ,Îµ-unsaturated ββ-difluoro-α-diazo esters, the direct formation of bicyclo[2.1.0]pentane ring systems via intramolecular cyclopropanation

W. Cai, G. Shi, 1996 .

Rhodium‐Catalyzed Decomposition of δ,.epsilon.‐Unsaturated β ,β‐Difluoro‐α‐diazo Esters, the Direct Formation of Bicyclo( 2.1.0)pentane Ring Systems via Intramolecular Cyclopropanation.

W. Cai, G. Shi, 1997 .

A Facile Synthesis of α-Trifluorodiazo Compounds.

Yuanyao Xu, G. Shi, 1990 .

Total synthesis of brevetoxin A.

K. Nicolaou, K. A. Emmitte, J. Gunzner, 2009, Organic letters.

TOTAL SYNTHESIS OF BREVETOXIN A : PART 2 : SECOND GENERATION STRATEGY AND CONSTRUCTION OF EFGH MODEL SYSTEM

P. A. Wallace, M. Bunnage, K. Nicolaou, 1999 .