Research

Publications

1. Kotha, S.*; Agrawal, A.; Ansari, S. Synthesis of Angular Triquinane and [4.3.3]Propellane Derivatives via Ring-Rearrangement Olefin Metathesis. ChemistrySelect 2021, 6(41), 11178-11181.  doi.org/10.1002/slct.202103226

2. Kotha, S.*; Agrawal, A.; Tangella, Y. Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps. RSC Adv. 2022, 12, 14278-14281. doi.org/10.1039/D2RA01458K.

3. Kotha, S.*; Agrawal, A. Synthesis of Linear Tetraquinanes by [3+2] Cycloaddition, Chemoselective Allylation of 7-Ketonorbornene, and Ring-Rearrangement Metathesis as Key Steps. Synlett 2022, 34, 841-845. https://doi.org/10.1055/s-0042-1751365.

4. Kotha, S.*; Agrawal, A. Synthesis of linear cis-anti-cis triquinane derivative via a [3+2] Cycloaddition and Krapcho decarboxylation as key steps. Indian J. Chem. 2023, 62, 527-531. doi.org/10.56042/ijc.v62i5.1433

5. Kotha, S.*; Agrawal, A.; Keesari, R. R. Synthetic  Studies to exo-Ring-Junction based  Fused 5/5/n-Tricyclic  Systems: Access  to  A, B, C-Ring  System of  Longeracinphyllin A, Himalenine  D, and Daphnipaxiamine A. Asian J. Org. Chem. 2023, e202300179. doi.org/10.1002/ajoc.202300179

6. Kotha, S.*; Agrawal, A. Linear tetraquinanes by microwave assisted [3+2] cycloaddition and ring-rearrangement metathesis. ChemistrySelect 2023, 8, e202302017. doi.org/10.1002/slct.202302017

7. Kotha, S.*; Agrawal, A. Synthesis of macrocyclic musk-like compounds through ring expansion metathesis and Tebbe olefination as key steps. Chemist rySelect 2023, 8, e202301971. doi.org/10.1002/slct.202301971