D. Barma

发表

Inhibition of telomerase by BIBR 1532 and related analogues.

D. Corey, J. Falck, D. Barma, 2003, Bioorganic & medicinal chemistry letters.

A tagging-via-substrate technology for detection and proteomics of farnesylated proteins.

F. Tamanoi, Yingming Zhao, Y. Kho, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Tagging-via-substrate strategy for probing O-GlcNAc modified proteins.

Yingming Zhao, J. Falck, Sung Chan Kim, 2005, Journal of proteome research.

Stereoselective Total Synthesis of 5(S), 6(R), 15(S)-Trihydroxy-7(E), 9(E), 11(Z),13(E)-Eicosatetraenoic Acid (Lipoxin A)

D. Barma, J. Yadav, D. Dutta, 1998 .

Asymmetric synthesis of the stereoisomers of 11,12,15(S)-trihydroxyeicosa-5(Z),8(Z),13(E)-trienoic acid, a potent endothelium-derived vasodilator.

J. Falck, W. Campbell, D. Barma, 2004, Bioorganic & medicinal chemistry letters.

Chiral α,β-Dialkoxy- and α-Alkoxy-β-aminostannanes: Preparation and Copper-Mediated Cross-Coupling

J. Falck, J. Capdevila, D. Barma, 2003 .

19-Hydroxyeicosatetraenoic acid analogs: Antagonism of 20-hydroxyeicosatetraenoic acid-induced vascular sensitization and hypertension.

J. Falck, D. Barma, V. Garcia, 2019, Bioorganic & medicinal chemistry letters.

A highly efficient practical method for the synthesis of chiral polyhydroxy-(E,E)-1-chlorodienols and (E)-5-hydroxy enynes

D. Barma, J. Yadav, D. Dutta, 1997 .

Zinc mediated deoxygenation of 4-hydroxy-2-butenoic acid moiety. An application for the synthesis of multifunctional chiral synthon

D. Barma, J. Yadav, 1996 .

A highly stereospecific synthesis of (E)-α,β-unsaturated esters

J. Falck, C. Mioskowski, D. Barma, 2004 .

A convenient preparation of 3-substituted furans: synthesis of perillene and dendrolasin.

J. Falck, C. Mioskowski, D. Barma, 2002, Organic letters.

Ring expansion/homologation--aldehyde condensation cascade using tert-trihalomethylcarbinols.

J. Falck, R. Akella, C. Mioskowski, 2006, Organic letters.

A versatile synthesis of 2-haloalk-2(Z)-en-1-ols and 1-chloro-1(Z)-alkenes from trichloromethylcarbinols

J. Falck, C. Mioskowski, D. Barma, 2002 .

Reductive olefination of aldehydes via chromium Brook rearrangement.

J. Falck, C. Mioskowski, D. Barma, 2006, Organic letters.

Differential Cleavage of Arylmethyl Ethers: Reactivity of 2,6‐Dimethoxybenzyl Ethers

J. Falck, C. Mioskowski, D. Barma, 2001 .

Regioselective de-O-benzylation of monosaccharides

J. Falck, C. Mioskowski, D. Barma, 2002 .

Stereoselective transformations of trihalomethylcarbinols induced by chromous chloride.

J. Falck, C. Mioskowski, D. Barma, 2005, Angewandte Chemie.

Convenient preparation of (Z)-α-halo-α,β-unsaturated aldehydes: synthesis of a Laurencia flexilis toxin

J. Falck, C. Mioskowski, D. Barma, 2008 .

Chromium vinylidene carbenoids: stereospecific synthesis of (Z)-2-chloroalk-2-en-1-ols.

J. Falck, A. Valleix, C. Mioskowski, 2001, Organic letters.

Stereoselective CrCl2-mediated condensation of aldehydes with functionalized 1,1,1-trichlorides: synthesis of trisubstituted (Z)-chloroolefins

J. Falck, D. Barma, Dong-Soo Shin, 2004 .

Three-component synthesis of 2-haloalk-2(Z)-en-1-ols via tandem haloalkylidenation-aldehyde addition

J. Falck, C. Mioskowski, D. Barma, 2002 .

A convenient synthesis of 2-tetrahydrofuranyl ethers.

J. Falck, A. Valleix, C. Mioskowski, 2000, Organic letters.

α-chlorovinylation: Synthesis of 2-chloropropenyl and propargyl alcohols

J. Falck, C. Mioskowski, D. Barma, 1999 .

Chiral α,β‐Dialkoxy‐ and α‐Alkoxy‐β‐aminostannanes: Preparation and Copper‐Mediated Cross‐Coupling.

J. Falck, J. Capdevila, D. Barma, 2004 .

Chromium vinylidene carbenoids: generation, characterization, and reactivity. First evidence for an internal proton return phenomenon with vinylidene carbenoids.

J. Falck, C. Mioskowski, D. Barma, 2001, Journal of the American Chemical Society.

Cascade synthesis of (E)-2-alkylidenecyclobutanols.

J. Falck, D. Barma, R. Baati, 2009, Organic letters.

Dimethylthiocarbamate (DMTC): an alcohol protecting group.

J. Falck, J. Capdevila, D. Barma, 2003, Organic letters.

Requirement of Inositol Pyrophosphates for Full Exocytotic Capacity in Pancreatic β Cells

A. Saiardi, J. Gromada, J. Falck, 2007, Science.

Global identification of O-GlcNAc-modified proteins.

Animesh Nandi, Yingming Zhao, J. Falck, 2006, Analytical chemistry.

Structural Analysis and Detection of Biological Inositol Pyrophosphates Reveal That the Family of VIP/Diphosphoinositol Pentakisphosphate Kinases Are 1/3-Kinases*

J. York, G. Mayr, J. Falck, 2009, Journal of Biological Chemistry.

Fe(0)-mediated synthesis of tri- and tetra-substituted olefins from carbonyls: an environmentally friendly alternative to Cr(II).

J. Falck, C. Mioskowski, D. Barma, 2006, The Journal of organic chemistry.

(Z)-alpha-haloacrylates: an exceptionally stereoselective preparation via Cr(II)-mediated olefination of aldehydes with trihaloacetates.

J. Falck, C. Mioskowski, D. Barma, 2003, Journal of the American Chemical Society.