Intramolecular Diels–Alder reaction as a key step in tandem or sequential processes: a versatile tool for the synthesis of fused and bridged bicyclic or polycyclic compounds.
IR@NIO: CSIR-National Institute Of Oceanography, Goa
View Archive Info| Field | Value | |
| Creator |
Parvatkar, P.T.
Kadam, H.K. Tilve, S.G. |
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| Date |
2014-09-04T07:08:47Z
2014-09-04T07:08:47Z 2014 |
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| Identifier |
Tetrahedron, vol.70(18); 2014; 2857-2888.
http://drs.nio.org/drs/handle/2264/4593 |
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| Description |
This review summarizes the recent examples of tandem or sequential reactions used for the last 10 years for the synthesis of fused and bridged bicyclic or polycyclic compounds with IMDA cycloaddition as the key means to access these compounds. Tandem or sequential processes are economically highly efficient and if properly planned and executed can provide facile route for the synthesis of complex natural product skeletons.
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| Language |
en
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| Publisher |
Elsevier
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| Rights |
An edited version of this paper was published by Elsevier. Copyright [2014] Elsevier
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| Subject |
Natural product
Sequential |
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| Title |
Intramolecular Diels–Alder reaction as a key step in tandem or sequential processes: a versatile tool for the synthesis of fused and bridged bicyclic or polycyclic compounds.
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| Type |
Journal Article
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