Metadata of CSIR Papers
View Archive Info| Field | Value | |
| Creator |
George, SC
John, J Anas, S John, J Yamamoto, Y Suresh, E Radhakrishnan, KV |
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| Subject |
Chemistry
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| Description |
An effective protocol has been developed for the construction of 3,3-disubstituted indol-2-ones from isatylidenes by utilizing amphiphilic bis-pi-allylpalladium and related intermediates. The developed strategy is a new method for the quaternization of position 3 of the indol-2-one towards disubstituted functionalized indol-2-ones. These products were subjected to ring-closing metathesis towards the synthesis of spiro[cyclohexene-1,3 '-indol]-2 '-ones and spiro[oxep-5-ene-2,3 '-indol]-2 '-ones, which are of biological interest.
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| Publisher |
WILEY-BLACKWELLMALDENCOMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USA
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| Date |
2011-09-20T12:03:10Z
2011-09-20T12:03:10Z 2010 |
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| Type |
Article
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| Identifier |
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
1434-193X http://hdl.handle.net/123456789/12204 |
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| Language |
English
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