Design and synthesis of novel bis-annulated caged polycycles via ring-closing metathesis: pushpakenediol

Scholarly Works

• Kotha, S.; Mehta, G.; Jena, K. Synthetic Approach toward Diverse Oxa-Cages via Olefin Metathesis. The Journal of organic chemistry 2024, 89, 5952–5965. doi:10.1021/acs.joc.3c02624
• Kotha, S.; Chaurasia, U. N.; Jena, K. Ring‐Rearrangement Metathesis Approach to Fused [5/5/6/5/5] and [6/5/5/5/5/6] Carbocyclic Derivatives. ChemistrySelect 2023, 8. doi:10.1002/slct.202302094
• Kotha, S.; Nandan Chaurasia, U.; Ansari, S. Early and Late‐Stage Functionalization of Cage Systems: Stereochemically Divergent Synthesis of Oxa‐cages via Olefin Metathesis. ChemistrySelect 2022, 7. doi:10.1002/slct.202202497
• Kotha, S.; Cheekatla, S. R.; Chaurasia, U. N. Annulated oxa-cage frameworks via Claisen rearrangement and ring-closing metathesis. Tetrahedron 2020, 76, 131694. doi:10.1016/j.tet.2020.131694
• Kotha, S.; Cheekatla, S. R.; Meshram, M. Design and Synthesis of Cage Molecules as High Energy Density Materials for Aerospace Applications. ChemCatChem 2020, 12, 6131–6172. doi:10.1002/cctc.202001475
• Bartolo, N. D.; Read, J. A.; Valentín, E. M.; Woerpel, K. A. Reactions of Allylmagnesium Reagents with Carbonyl Compounds and Compounds with C═N Double Bonds: Their Diastereoselectivities Generally Cannot Be Analyzed Using the Felkin-Anh and Chelation-Control Models. Chemical reviews 2020, 120, 1513–1619. doi:10.1021/acs.chemrev.9b00414
• Kotha, S.; Meshram, M. Application of Claisen Rearrangement and Olefin Metathesis in Organic Synthesis. Chemistry, an Asian journal 2018, 13, 1758–1766. doi:10.1002/asia.201800613
• Kotha, S.; Meshram, M.; Dommaraju, Y. Design and Synthesis of Polycycles, Heterocycles, and Macrocycles via Strategic Utilization of Ring-Closing Metathesis. Chemical record (New York, N.Y.) 2018, 18, 1613–1632. doi:10.1002/tcr.201800025
• Kotha, S.; Cheekatla, S. R. A New Synthetic Approach to C2‐Symmetric Octacyclic Cage Diol via Claisen Rearrangement and Ring‐Closing Metathesis as Key Steps. ChemistrySelect 2017, 2, 6877–6881. doi:10.1002/slct.201701633
• Kotha, S.; Cheekatla, S. R.; Mandal, B. Synthesis and Rearrangement of Cage [4.3.2]Propellanes that Contain a Spiro Linkage. European Journal of Organic Chemistry 2017, 2017, 4277–4282. doi:10.1002/ejoc.201700617
• Kotha, S.; Panguluri, N. R.; Ali, R. Design and Synthesis of Spirocycles. European Journal of Organic Chemistry 2017, 2017, 5316–5342. doi:10.1002/ejoc.201700439
• Kotha, S.; Cheekatla, S. R.; Chinnam, A. K.; Jain, T. Design and synthesis of polycyclic bisindoles via Fischer indolization and ring-closing metathesis as key steps. Tetrahedron Letters 2016, 57, 5605–5607. doi:10.1016/j.tetlet.2016.10.112
• Herndon, J. W. The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2014. Coordination Chemistry Reviews 2016, 317, 1–121. doi:10.1016/j.ccr.2015.09.012
• Poplata, S.; Tröster, A.; Zou, Y.-Q.; Bach, T. Recent Advances in the Synthesis of Cyclobutanes by Olefin [2+2] Photocycloaddition Reactions. Chemical reviews 2016, 116, 9748–9815. doi:10.1021/acs.chemrev.5b00723
• Kotha, S.; Saifuddin, M.; Ali, R.; Sreevani, G. Spiro annulation of cage polycycles via Grignard reaction and ring-closing metathesis as key steps. Beilstein journal of organic chemistry 2015, 11, 1367–1372. doi:10.3762/bjoc.11.147
• Kotha, S.; Chavan, A. S.; Goyal, D. Diversity-Oriented Approaches to Polycyclics and Bioinspired Molecules via the Diels-Alder Strategy: Green Chemistry, Synthetic Economy, and Beyond. ACS combinatorial science 2015, 17, 253–302. doi:10.1021/co500146u

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