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Ramakrishna Reddy Keesari

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Articles

Creation of Diversity in Polyquinane Synthesis Involving Metathesis as a Key Step

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By Sambasivarao Kotha, Ramakrishna Reddy Keesari, Subba Rao Cheekatla
| Wiley Online Library Verified
Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available from the corresponding author upon reasonable request. References 1 and , Chemical Reviews 97 (1997): 671–720. 2 and , “ Synthesis of Triquinane Natural Products,” in Polyquinane Chemistry: Syntheses and Reactions, ed. L. A. Paquette and A. M. Doherty (Springer Berlin Heidelberg, 1987), 169–208.
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Design and Synthesis of Linearly Fused Triquinanes through Tandem‐Metathesis: Access to Basic Core of Cucumin, Capnellene, Chondrosterin, and Xeromphalinone

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By Sambasivarao Kotha, Ramakrishna Reddy Keesari
| Wiley Online Library Verified
Research Article Graphical Abstract A tandem-metathesis approach to linearly fused tricyclic enone 1 and cis-anti-cis-type hydroxy-triquinane 2 has been described in an efficient manner starting with exo-dicyclopentadiene-1-one. The tricyclic enone 1 was found to be a core unit of triquinane-based natural products such as cucumin, capnellene, chondrosterin, and xeromphalinone.
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