dongari yadagiri - Catalysis

Author Information

Dongari Yadagiri is a researcher affiliated with the Department of Chemistry, Laboratory of Organic Synthesis & Catalysis at the Indian Institute of Technology Roorkee, located in Roorkee-247667, Uttarakhand, India. His work focuses on the field of catalysis and organic synthesis.

Research Contributions

Dongari Yadagiri has made significant contributions to the field of catalysis, particularly in the areas of metallocarbenes, denitrogenative transformations, and radical relay reactions. His research includes innovative methods for the functionalization of metallocarbenes derived from α-diazocarbonyl compounds, light-free directed amination of remote unactivated C(sp3)-H bonds of alcohols, and light-induced metal-free transformations of unactivated pyridotriazoles. Additionally, his work on the Rhodium catalyzed synthesis of benzopyrans and micelle-enabled clean sulfonylation of polyfluoroarenes in water under mild conditions has been well-received in the scientific community.

Aliases

There are no aliases listed for Dongari Yadagiri.

Publication and Citation Metrics

Metric	Value
Total Citation Count	818
h-index	12
Total Paper Count	20

Publications:

Catalytic Functionalization of Metallocarbenes Derived from α‐Diazocarbonyl Compounds and Their Precursors

DOI: 10.1002/tcr.202100167

Year: 2021

Denitrogenative Transformations of Pyridotriazoles and Related Compounds: Synthesis of N-Containing Heterocyclic Compounds and Beyond.

DOI: 10.1021/acs.joc.0c01652

Year: 2020

Transition-Metal- and Light-Free Directed Amination of Remote Unactivated C(sp3)-H Bonds of Alcohols.

DOI: 10.1021/jacs.9b04189

Year: 2019

Aliphatic Radical Relay Heck Reaction at Unactivated C(sp3 )-H Sites of Alcohols.

DOI: 10.1002/anie.201812398

Year: 2019

Light-induced metal-free transformations of unactivated pyridotriazoles† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c9sc02448d

DOI: 10.1039/C9SC02448D

Year: 2019

Rhodium Catalyzed Synthesis of Benzopyrans via Transannulation of N-Sulfonyl-1,2,3-triazoles with 2-Hydroxybenzyl Alcohols.

DOI: 10.1021/acs.orglett.8b01338

Year: 2018

Aliphatic Radical Relay Heck Reaction at Unactivated C(sp3)–H Sites of Alcohols

DOI: 10.26434/chemrxiv.7108304

Year: 2018

Micelle-enabled clean and selective sulfonylation of polyfluoroarenes in water under mild conditions

DOI: 10.1039/C7GC03514D

Year: 2018

Aliphatic Radical Relay Heck Reaction at Unactivated C(sp3)–H Sites of Alcohols

DOI: 10.26434/chemrxiv.7108304.v1

Year: 2018

One‐Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

DOI: 10.1002/CHIN.201614111

Year: 2016

What is Predictive Accuracy in Catalysis?

What are their Theoretical Contributions?

Can Reactor Design Influence Engagement?

What Are Access Restrictions in Catalysis?

What are the Key Criteria for Tracer Selection?

What Are the Solutions to Improper Scaling?

What Are Some Common NMR Techniques Used in Catalysis?

Can Environmental Variability Be Controlled?

What are the Challenges in Reducing Catalyst Loading?

How is Maltose Hydrolyzed?

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