Srikrishna, A. (1987) Radical cyclizations in the synthesis of natural products Current Science, 56 (9). pp. 392-396. ISSN 0011-3891
Full text not available from this repository.
Official URL: http://www.ias.ac.in/j_archive/currsci/56/9/392-39...
Abstract
Organic chemists have began to use intramolecular radical addition reactions i.e. radical cyclization to develop useful synthetic transformations. The mild reactions conditions and the observed selectivities made these radical cyclizaiona a viable alternative to the conventional polar reactions. Applicatin of polar radical cyclization strategy to various natural products like sesquiterpenes (sativenes, agarofuransm, hirsutene, capnellenes, silphiperfolene, seychellene, patchoulli alcohol), marine deterpene isoamijiol, pyrrolizidine alkaloids. (dehydrohastanecine, heliotridine, hastanecine), by various organic chemists demonstrates the versatility of this relatively new area in organic synthesis.
Item Type: | Article |
---|---|
Source: | Copyright of this article belongs to Current Science Association. |
ID Code: | 48808 |
Deposited On: | 15 Jul 2011 12:27 |
Last Modified: | 15 Jul 2011 12:27 |
Repository Staff Only: item control page