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Perla Bharath Kumar

As seen in: Wiley Online Library, ACS Publications
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Articles

Transition-Metal-Catalyzed Carbon-Carbon Cross-Coupling: Synthesis of α-Chiral Allylic Amines

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By Hao-Ran Zhang, Yao Wang, Perla Bharath Kumar
| Wiley Online Library Verified
1 Introduction α-Chiral allylic amines serve as key structural units in natural products, bioactive compounds, and therapeutic agents (Scheme 1a) [1-9]. Moreover, α-chiral allylic amines also serve as backbones for chiral catalysts and versatile chiral synthons for value-added targets due to the orthogonal reactivity of alkenes over amines [10-12].
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Visible-Light Catalyzed Functionalizations of Allylic C–H Bonds

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By jing jia zhang, Haoran Zhang, Perla Bharath Kumar
| Wiley Online Library Verified
Zhang, J., Zhang, H., Kumar, P.B., Li, Y., Yu, Q. and Shu, W. (2026), Visible-Light Catalyzed Functionalizations of Allylic C–H Bonds. Chin. J. Chem.. https://doi.org/10.1002/cjoc.70595 References 1 ; ; ; Transition-Metal- Catalyzed C–H Allylation Reactions. Chem 2021, 7, 555–605. 2 Metal Catalyzed Allylic Alkylation: Its Development in the Trost Laboratories. Tetrahedron 2015, 71, 5708–5733. 3 Fundamentals of Green Chemistry: Efficiency in Reaction Design. Chem. Soc. Rev. 2012, 41, 1437–1451.
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Regio‐ and Stereoselective Intramolecular Protocol to Access Dihydropyrano[3,4‐b]indol‐1(3H)‐ones via a Tandem C‐3 Propargylation/Cycloisomerization

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By Perla Bharath Kumar, Balasubramanian Sridhar, Patil Sagar Pradip, Noufia Rahman
| Wiley Online Library Verified
Conflict of Interest The authors declare no conflict of interest. Data Availability Statement The data supporting this article have been included as part of the ESI. Supporting Information Filename Description adsc70164-sup-0001-SuppData-S1.pdf3.5 MB Supplementary Material References 1, the Chemistry of Indoles, Academic Press, New York 1970. 2, , , , , Mini-Rev. Med. Chem. 2013, 13, 1792. 3, , Chem. Sci. 2013, 4, 29. 4, , Bioorg. Chem. 2019, 89, 103021. 5, , Adv. Synth. Catal. 2009, 351, 2005.
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