Surisetti Suresh
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View article: Benzothiazolo-quinazoline Congeners Function as Anti-microtubule Agents Triggering Mitotic Arrest in Cancer Cells
Benzothiazolo-quinazoline Congeners Function as Anti-microtubule Agents Triggering Mitotic Arrest in Cancer Cells Open
Background Antimicrotubule agents effectively block cancer spread and are routinely employed as front-line chemotherapeutics. But patients, who receive Paclitaxel, suffer from peripheral neuropathy, which not only lowers quality of life bu…
View article: Design and application of intramolecular arylogous nitroaldol condensation to access 2-aryl-benzofuran and -indole derivatives and formal synthesis of saprisartan
Design and application of intramolecular arylogous nitroaldol condensation to access 2-aryl-benzofuran and -indole derivatives and formal synthesis of saprisartan Open
An intramolecular arylogous nitroaldol condensation has been developed for the synthesis of benzoheterols under transition metal-free conditions and synthesized an advanced key intermediate of saprisartan—thus constituting a formal synthes…
View article: CCDC 2266291: Experimental Crystal Structure Determination
CCDC 2266291: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: Front Cover: Photocatalyzed Energy Transfer for Atom Economical Synthesis of O‐Bridged Tricyclo‐Fused Cyclopropane Derivatives (Eur. J. Org. Chem. 45/2023)
Front Cover: Photocatalyzed Energy Transfer for Atom Economical Synthesis of O‐Bridged Tricyclo‐Fused Cyclopropane Derivatives (Eur. J. Org. Chem. 45/2023) Open
The Front Cover illustrates the exploration of new chemical space aiding drug discovery research programs. The precise strategic and sustainable methods must be established to explore the molecular complexity of the chemical structures. He…
View article: CCDC 2278284: Experimental Crystal Structure Determination
CCDC 2278284: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2278285: Experimental Crystal Structure Determination
CCDC 2278285: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 1887440: Experimental Crystal Structure Determination
CCDC 1887440: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2150989: Experimental Crystal Structure Determination
CCDC 2150989: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2195309: Experimental Crystal Structure Determination
CCDC 2195309: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2128795: Experimental Crystal Structure Determination
CCDC 2128795: Experimental Crystal Structure Determination Open
View article: N-Heterocyclic carbene (NHC)-catalyzed oxidation of unactivated aldimines to amides <i>via</i> imine umpolung under aerobic conditions
N-Heterocyclic carbene (NHC)-catalyzed oxidation of unactivated aldimines to amides <i>via</i> imine umpolung under aerobic conditions Open
A general NHC-catalyzed conversion of imines to amides proceeding through umpolung–oxidation under aerobic conditions in green solvent is reported.
View article: CCDC 2047920: Experimental Crystal Structure Determination
CCDC 2047920: Experimental Crystal Structure Determination Open
View article: CCDC 2047921: Experimental Crystal Structure Determination
CCDC 2047921: Experimental Crystal Structure Determination Open
View article: CCDC 2076652: Experimental Crystal Structure Determination
CCDC 2076652: Experimental Crystal Structure Determination Open
View article: CCDC 2076651: Experimental Crystal Structure Determination
CCDC 2076651: Experimental Crystal Structure Determination Open
View article: CCDC 1982965: Experimental Crystal Structure Determination
CCDC 1982965: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: Ruthenium Catalyzed Regioselective β‐C(<i>sp</i><sup>3</sup>)−H Functionalization of <i>N</i>‐Alkyl‐<i>N′</i>‐<i>p–</i>nitrophenyl Substituted Piperazines using Aldehydes as Alkylating Agents
Ruthenium Catalyzed Regioselective β‐C(<i>sp</i><sup>3</sup>)−H Functionalization of <i>N</i>‐Alkyl‐<i>N′</i>‐<i>p–</i>nitrophenyl Substituted Piperazines using Aldehydes as Alkylating Agents Open
Herein, we disclose a ruthenium‐catalyzed regioselective β‐C( sp 3 )−H bond functionalization on the piperazine core using aldehydes as alkylating agents. The present transformation appears to go through the dehydrogenation of the piperazi…
View article: CCDC 1960496: Experimental Crystal Structure Determination
CCDC 1960496: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 1960494: Experimental Crystal Structure Determination
CCDC 1960494: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 1960497: Experimental Crystal Structure Determination
CCDC 1960497: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 1960495: Experimental Crystal Structure Determination
CCDC 1960495: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 1912875: Experimental Crystal Structure Determination
CCDC 1912875: Experimental Crystal Structure Determination Open
View article: Direct Access to (±)‐10‐Desbromoarborescidine A from Tryptamine and Pentane‐1,5‐diol
Direct Access to (±)‐10‐Desbromoarborescidine A from Tryptamine and Pentane‐1,5‐diol Open
A single step synthetic strategy for (±)10‐ desbromoarborescidine A is described. Starting from tryptamine and pentane‐1,5‐diol, this acceptorless dehydrogenative condensation process is efficiently catalyzed by a ruthenium complex featuri…
View article: CCDC 1953542: Experimental Crystal Structure Determination
CCDC 1953542: Experimental Crystal Structure Determination Open
View article: Substrate controlled, regioselective carbopalladation for the one-pot synthesis of C4-substituted tetrahydroisoquinoline analogues
Substrate controlled, regioselective carbopalladation for the one-pot synthesis of C4-substituted tetrahydroisoquinoline analogues Open
6-Exo-trig cyclization reaction through regioselective carbopalladation was demonstrated with N-(2-halobenzyl)-N-allylamines to furnish the corresponding C4-substituted tetrahydroisoquinoline derivatives.
View article: Direct Access to (±)-10-Desbromoarborescidine A from Tryptamine and Pentan-1,5-diol
Direct Access to (±)-10-Desbromoarborescidine A from Tryptamine and Pentan-1,5-diol Open
A single step synthetic strategy for (±)10- Desbromoarborescidine A is described. Starting from tryptamine and pentan-1,5-diol, this acceptorless dehydrogenative condensation process is efficiently catalyzed by a ruthenium complex featurin…
View article: Direct Access to (±)-10-Desbromoarborescidine A from Tryptamine and Pentan-1,5-diol
Direct Access to (±)-10-Desbromoarborescidine A from Tryptamine and Pentan-1,5-diol Open
A single step synthetic strategy for (±)10- Desbromoarborescidine A is described. Starting from tryptamine and pentan-1,5-diol, this acceptorless dehydrogenative condensation process is efficiently catalyzed by a ruthenium complex featurin…
View article: CCDC 1887439: Experimental Crystal Structure Determination
CCDC 1887439: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: Ruthenium Phosphine–Pyridone Catalyzed Cross-Coupling of Alcohols To form α-Alkylated Ketones
Ruthenium Phosphine–Pyridone Catalyzed Cross-Coupling of Alcohols To form α-Alkylated Ketones Open
An efficient and green route to access diverse functionalized ketones via dehydrogenative-dehydrative cross-coupling of primary and secondary alcohols is demonstrated. Selective and tunable formation of ketones or alcohols is catalyzed by …
View article: Ruthenium catalyzed β-C(sp<sup>3</sup>)–H functionalization on the ‘privileged’ piperazine nucleus
Ruthenium catalyzed β-C(sp<sup>3</sup>)–H functionalization on the ‘privileged’ piperazine nucleus Open
Ruthenium catalysed β-C(sp3)–H functionalization of piperazines has been revealed.