Synthetic approach to cis and trans-decalins via Diels-Alder reaction and ring-closing metathesis as key steps: further extension to dioxapropellane derivative by ring-closing metathesis

Kotha, Sambasivarao ; Chavan, Arjun S. ; Dipak, Mirtunjay Kumar (2011) Synthetic approach to cis and trans-decalins via Diels-Alder reaction and ring-closing metathesis as key steps: further extension to dioxapropellane derivative by ring-closing metathesis Tetrahedron, 67 (2). pp. 501-504. ISSN 0040-4020

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tet.2010.10.080

Abstract

9,10-Substituted cis and trans-decalins were synthesized by a simple route using the Diels-Alder reaction and ring-closing metathesis (RCM) as key steps. Later, the cis-decalin system has been extended to 3,8-dioxa[8.4.4]propellane derivative by RCM sequence as a key step.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Diels-Alder Reaction; Ring-closing Metathesis; Decalin; Propellane; Hydrogenation
ID Code:65171
Deposited On:15 Oct 2011 11:48
Last Modified:15 Oct 2011 11:48

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