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
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Title |
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
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Creator |
KOTHA, S
CHAVAN, AS DIPAK, MK |
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Subject |
OLEFIN-METATHESIS
CATALYTIC METATHESIS ANTIBIOTIC BRANIMYCIN ALKENE METATHESIS VICINAL DIESTERS NOBEL LECTURE PROPELLANES ALPHA,OMEGA-DIHALIDES MACROCYCLES CARBON Diels-Alder reaction Ring-closing metathesis Decalin Propellane Hydrogenation |
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Description |
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. (C) 2010 Elsevier Ltd. All rights reserved.
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Publisher |
PERGAMON-ELSEVIER SCIENCE LTD
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Date |
2012-06-26T08:37:40Z
2012-06-26T08:37:40Z 2011 |
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Type |
Article
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Identifier |
TETRAHEDRON,67(2)501-504
0040-4020 http://dx.doi.org/10.1016/j.tet.2010.10.080 http://dspace.library.iitb.ac.in/jspui/handle/100/14200 |
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Language |
English
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