Sudhir M. Hande

发表

Total synthesis of aspergillide B and structural discrepancy of aspergillide A

Sudhir M. Hande, J. Uenishi, 2009 .

Photochemistry of mycolactone A/B, the causative toxin of Buruli ulcer.

Y. Kishi, Sudhir M. Hande, Y. Xing, 2012, Journal of the American Chemical Society.

Discovery of a Series of 7-Azaindoles as Potent and Highly Selective CDK9 Inhibitors for Transient Target Engagement.

A. Ferguson, L. Drew, W. Shao, 2021, Journal of medicinal chemistry.

α-Heteroarylation of Thioethers via Photoredox and Weak Brønsted Base Catalysis.

Sudhir M. Hande, Edwin Alfonzo, 2021, Organic letters.

Palladium-catalyzed intramolecular carboborylation of 1,3-diene and synthesis of ABCD ring of communesins.

C. Tsukano, Y. Takemoto, Sudhir M. Hande, 2019, Organic & biomolecular chemistry.

Preparation of highly functionalized 1,5-disubstituted tetrazoles via palladium-catalyzed Suzuki coupling

E. Hennessy, V. Hoesch, Sudhir M. Hande, 2017 .

Flexible Strategy for Syntheses of Spirooxindoles Using Palladium‐Catalyzed Carbosilylation and Sakurai‐Type Cyclization.

C. Tsukano, Y. Takemoto, Sudhir M. Hande, 2011 .

Photoredox mediated C N cross coupling of sulfoximines with aryl iodides

A. Mfuh, Qing Ye, Sudhir M. Hande, 2019, Tetrahedron Letters.

Stereoselective synthesis of (-)-diospongins A and B and their stereoisomers at C-5

Sudhir M. Hande, J. Uenishi, N. Kawai, 2007 .

Flexible strategy for syntheses of spirooxindoles using palladium-catalyzed carbosilylation and Sakurai-type cyclization.

C. Tsukano, Y. Takemoto, Sudhir M. Hande, 2011, Organic letters.

Stereochemistry of intermolecular oxypalladation: Pd(II)-catalyzed 1,3-chirality transfer reaction of chiral allylic alcohol with methanol.

Y. Vikhe, Sudhir M. Hande, J. Uenishi, 2009, The Journal of organic chemistry.

Photoredox and Weak Brønsted Base Dual Catalysis: Alkylation of α-Thio Alkyl Radicals

Sudhir M. Hande, Edwin Alfonzo, 2020 .

Discovery of AZD4573, a Potent and Selective Inhibitor of CDK9 That Enables Short Duration of Target Engagement for the Treatment of Hematological Malignancies.

A. Ferguson, L. Drew, W. Shao, 2020, Journal of medicinal chemistry.

Discovery of 5-{4-[(7-Ethyl-6-oxo-5,6-dihydro-1,5-naphthyridin-3-yl)methyl]piperazin-1-yl}-N-methylpyridine-2-carboxamide (AZD5305): A PARP1-DNA Trapper with High Selectivity for PARP1 over PARP2 and Other PARPs.

Fiona Pachl, A. Pike, M. O’Connor, 2021, Journal of medicinal chemistry.

Mechanistic Insights into a CDK9 Inhibitor Via Orthogonal Proteomics Methods.

J. A. Hendricks, L. Reiter, D. M. Molina, 2021, ACS chemical biology.

Synthesis and structure of two new mycolactones isolated from M. ulcerans subsp. shinshuense.

Y. Kazumi, Y. Kishi, W. G. Lai, 2012, Organic Letters.

Discovery of AZD9833, a potent and orally bioavailable selective estrogen receptor degrader and antagonist.

O. Delpuech, J. Breed, J. Nissink, 2020, Journal of medicinal chemistry.

General methods for the synthesis and late-stage diversification of 2,4-substituted 7-azaindoles

Rebecca E. Meadows, B. Barlaam, Bryan E. Roberts, 2016 .

Discovery of a Potent and Orally Bioavailable Zwitterionic Series of Selective Estrogen Receptor Degrader-Antagonists.

J. Breed, J. Nissink, Paul R. J. Davey, 2023, Journal of medicinal chemistry.

An efficient synthesis of 2- and 2,6-substituted piperidines using Pd(II)-catalyzed 1,3-chirality transfer reaction.

Sudhir M. Hande, J. Uenishi, N. Kawai, 2009, The Journal of organic chemistry.