Recent applications of ring-rearrangement metathesis in organic synthesis

Scholarly Works

• Semghouli, A.; Drahos, L.; Volk, B.; Kiss, L. Selective Transformation of 1,3‐Cyclooctadiene into Novel Functionalized Azaheterocycles, β‐Amino Esters, and Lactams by Means of Ring‐Rearrangement Metathesis. European Journal of Organic Chemistry 2024. doi:10.1002/ejoc.202400170
• Weber, F.; Weber, A.; Schmitt, L.; Lechtenberg, I.; Greb, J.; Henßen, B.; Wesselborg, S.; Pietruszka, J. From the Total Synthesis of Semi-Viriditoxin, Semi-Viriditoxic Acid and Dimeric Naphthopyranones to their Biological Activities in Burkitt B Cell Lymphoma. Chemistry (Weinheim an der Bergstrasse, Germany) 2024, e202400559. doi:10.1002/chem.202400559
• Semghouli, A.; Nonn, M.; Remete, A. M.; Fustero, S.; Kiss, L. Application of Metathesis Protocols to the Stereocontrolled Synthesis of some Functionalized β-Amino Esters and Azaheterocycles. Chemical record (New York, N.Y.) 2023, 23, e202300279. doi:10.1002/tcr.202300279
• Kotha, S.; Meher, P. Expanding the Diversity of Azepino [3,2,1‐hi] Indoles via Transition Metal‐based Strategies such as Cross‐coupling Reaction and Ring Closing Metathesis. Asian Journal of Organic Chemistry 2023, 12. doi:10.1002/ajoc.202300287
• 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.; Agrawal, A. Synthesis of Macrocyclic Musk‐Like Compounds through Ring‐Expansion Metathesis and Tebbe Olefination as Key Steps. ChemistrySelect 2023, 8. doi:10.1002/slct.202301971
• Kotha, S.; Mehta, G. Molecular Acrobatics in Polycyclic Frames: Synthesis of "Kurmanediol" via Post-synthetic Modification of Cage Molecules by Olefinic Metathesis. The Journal of organic chemistry 2023, 88, 11650–11660. doi:10.1021/acs.joc.3c00968
• Semghouli, A.; Remete, A. M.; Kiss, L. Stereocontrolled synthesis of some novel functionalized heterocyclic amino ester and amide derivatives with multiple stereocenters. RSC advances 2023, 13, 22769–22776. doi:10.1039/d3ra03866a
• 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 Journal of Organic Chemistry 2023, 12. doi:10.1002/ajoc.202300179
• Kotha, S.; Reddy Keesari, R. Synthetic Improvements and an Alternative Synthetic Approach to exo‐Dicyclopentadiene‐1‐one: A Useful Building Block for Cyclopentanoids. Asian Journal of Organic Chemistry 2023, 12. doi:10.1002/ajoc.202300046
• Kotha, S.; Reddy Keesari, R. Design and Synthesis of Linearly Fused Triquinanes through Tandem‐Metathesis: Access to Basic Core of Cucumin, Capnellene, Chondrosterin, and Xeromphalinone. European Journal of Organic Chemistry 2023, 26. doi:10.1002/ejoc.202300106
• Nilova, A.; Mannchen, M. D.; Noel, A. N.; Semenova, E.; Grenning, A. J. Vicinal stereocenters via asymmetric allylic alkylation and Cope rearrangement: a straightforward route to functionally and stereochemically rich heterocycles. Chemical science 2023, 14, 2755–2762. doi:10.1039/d2sc07021a
• Kotha, S.; Chaurasia, U. N. Polycyclic High-Density Cage Compounds via Cross Metathesis. Synthesis 2023, 55, 2151–2158. doi:10.1055/a-2047-6742
• Kotha, S.; Reddy Keesari, R.; Ravikumar, O. Synthesis of 1,3‐cis‐Fused Tricyclic System through Regio‐ and Stereoselective Epoxidation and Ring‐Rearrangement Metathesis: Access To Basic Core of Presilphiperfolanols. European Journal of Organic Chemistry 2023, 26. doi:10.1002/ejoc.202201448
• Kotha, S.; Salman, M.; Cheekatla, S. R. Synthesis of Pentacycloundecane (PCUD) Based Spiro-Pyrano-Cage Framework via Ring-Closing Metathesis. Molbank 2023, 2023, M1567. doi:10.3390/m1567
• Kotha, S.; Singh, D. Synthesis of New Glycoluril Derivatives via Ring-Closing Metathesis. HETEROCYCLES 2023, 106, 2125. doi:10.3987/com-23-14912
• 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
• Klein, M. T.; Krause, B. M.; Neudörfl, J.-M.; Kühne, R.; Schmalz, H.-G. Design and synthesis of a tetracyclic tripeptide mimetic frozen in a polyproline type II (PP2) helix conformation. Organic & biomolecular chemistry 2022, 20, 9368–9377. doi:10.1039/d2ob01857h
• Kotha, S.; Keesari, R. R. Design and Synthesis of Highly Decorated Oxa‐Cage Systems via Olefin Metathesis. Asian Journal of Organic Chemistry 2022, 12. doi:10.1002/ajoc.202200624
• Kotha, S.; Keesari, R. R. An Intramolecular Cycloetherification of Unactivated Olefinic Substrates Bearing endo-Alcohol: Access to Diversely Alkylated Oxa-Cage Derivatives Useful for Olefin-Metathesis. Chemistry, an Asian journal 2022, 17, e202200848. doi:10.1002/asia.202200848

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