Rengarajan Balamurugan

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 16

Top Topics

Molecular Docking

Electron Transfer

Room Temperature

Silver Nanoparticles

Top Venues

The Journal of organic chemistry

Organic & biomolecular chemistry

Chemistry (Weinheim an der Bergstrasse, Germany)

This page only lists publications with an associated author ORCID identifier.

Publications

Rina Raju Manwar, Rengarajan Balamurugan
Silver-Catalyzed Olefination of Aryl Aldehydes Using Propiolates. Chemistry (Weinheim an der Bergstrasse, Germany) 30 (48) (2024)
Vemula Arunkumar, Rengarajan Balamurugan
Brønsted acid-promoted synthesis of highly functionalized tetrahydrocarbazoles from diethyl ( E )-5-diazo-4-oxohex-2-enedioate. Organic & biomolecular chemistry (2024)
Rina Raju Manwar, Rengarajan Balamurugan
Silver-Catalyzed Olefination of Aryl Aldehydes Using Propiolates. Chemistry (Weinheim an der Bergstrasse, Germany) (2024)
Kolimi Sayyad Basha, Rengarajan Balamurugan
Gold(I)-Catalyzed Regioselective Hydroarylation of Propiolic Acid with Arylboronic Acids. Organic letters (2023)
Mou Mandal, Renuka Pradhan, Upakarasamy Lourderaj, Rengarajan Balamurugan
Dodging the Conventional Reactivity of o -Alkynylanilines under Gold Catalysis for Distal 7- endo - dig Cyclization. The Journal of organic chemistry (2023)
Yeruva Pavankumar Reddy, V Srinivasadesikan, Rengarajan Balamurugan, M C Lin, Shaik Anwar
Synthesis of tetrahydrochromenes and dihydronaphthofurans via a cascade process of [3 + 3] and [3 + 2] annulation reactions: mechanistic insight for 6- endo-trig and 5- exo-trig cyclisation. RSC advances 13 (9) (2023)
Yeruva Pavankumar Reddy, V Srinivasadesikan, Rengarajan Balamurugan, M C Lin, Shaik Anwar
Synthesis of tetrahydrochromenes and dihydronaphthofurans via a cascade process of [3 + 3] and [3 + 2] annulation reactions: mechanistic insight for 6- endo-trig and 5- exo-trig cyclisation. RSC advances 13 (9) (2023)
Mou Mandal, Renuka Pradhan, Upakarasamy Lourderaj, Rengarajan Balamurugan
Dodging the Conventional Reactivity of o -Alkynylanilines under Gold Catalysis for Distal 7- endo - dig Cyclization. The Journal of organic chemistry 88 (4) (2023)
Mou Mandal, Rengarajan Balamurugan
TfOH-promoted synthesis of indoles and benzofurans involving cyclative transposition of vinyl ketone. Chemical communications (Cambridge, England) 58 (70) (2022)
Golla Ramesh, Valmuri Srivardhan, Rengarajan Balamurugan
Ag(I)-catalyzed cyclization of o -alkynylacetophenones facilitated through acetal formation: synthesis of C3-naphthyl indole derivatives. Organic & biomolecular chemistry (2022)
Golla Ramesh, Bokka Venkat Ramulu, Rengarajan Balamurugan
Activation of o -Propargyl Alcohol Benzaldehydes under Acetalization Conditions for Intramolecular Electrophile Intercepted Meyer-Schuster Rearrangement. The Journal of organic chemistry 87 (13) (2022)
Chandrahas Tarigopula, Seetharaman Manojveer, Rengarajan Balamurugan
Synthesis of Highly Substituted Biaryls by the Construction of a Benzene Ring via In Situ Formed Acetals. The Journal of organic chemistry 86 (17) (2021)
Golla Ramesh, Rengarajan Balamurugan
Triflic Acid-Catalyzed Synthesis of Indole-Substituted Indane Derivatives via In Situ Formed Acetal-Facilitated Nucleophilic Addition and 4π-Electron-5-Carbon Electrocyclization Sequence. The Journal of organic chemistry 86 (23) (2021)
Mou Mandal, Shanmugam Sakthivel, Rengarajan Balamurugan
Brønsted/Lewis Acid-Promoted Site-Selective Intramolecular Cycloisomerizations of Aryl-Fused 1,6-Diyn-3-ones for Diversity-Oriented Synthesis of Benzo-Fused Fluorenes and Fluorenones and Naphthyl Ketones. The Journal of organic chemistry 86 (1) (2020)
Shanmugam Sakthivel, Rengarajan Balamurugan
Annulation of a Highly Functionalized Diazo Building Block with Indoles under Sc(OTf)3/Rh2(OAc)4 Multicatalysis through Michael Addition/Cyclization Sequence. The Journal of organic chemistry 83 (19) (2018)
Naganaboina Naveen, Rengarajan Balamurugan
Catalyst free synthesis of α-fluoro-β-hydroxy ketones/α-fluoro-ynols via electrophilic fluorination of tertiary propargyl alcohols using Selectfluor™ (F-TEDA-BF4). Organic & biomolecular chemistry 15 (9) (2018)