Title : Studies in synthesis of heterocyclic molecules using the baylis-hillman adducts

Type of Material: Thesis
Title: Studies in synthesis of heterocyclic molecules using the baylis-hillman adducts
Researcher: Rao, Jamjanam Srivardhana
Guide: Basavaiah, D
Department: School of Chemistry
Publisher: University of Hyderabad, Hyderabad
Place: Hyderabad
Year: 27/7/04
Language: English
Subject: Chemistry
Physical and Basic Sciences
Dissertation/Thesis Note: PhD
Fulltext: Shodhganga

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040__|aHYDR_500046|dIN-AhILN
041__|aeng
100__|aRao, Jamjanam Srivardhana|eResearcher
110__|aSchool of Chemistry|bUniversity of Hyderabad, Hyderabad|dHyderabad|ein
245__|aStudies in synthesis of heterocyclic molecules using the baylis-hillman adducts
260__|aHyderabad|bUniversity of Hyderabad, Hyderabad|c27/7/04
300__|a255p.|dDVD
500__|aAppendices p.127-235
502__|bPhD
520__|aThe recent developments in organic chemistry, medicinal chemistry and drug discovery demand the continuous evolution of convenient methodologies for atom economical construction of carbon-carbon bonds and functional group transformation strategies involving high levels of stereochemical control there by leading to the development of operationally simple processes for assembling the carbon structural framework. The Baylis-Hillman reaction is an emerging atom economical, carbon-carbon bond forming reaction involving the coupling of ot-position of activated alkenes with carbon electrophiles under the influence of a catalyst, most commonly a tertiary amine [in particular, l,4-diazabicyclo(2.2.2)octane (DABCO)] producing multifunctional molecules, whose applications in a number of organic transformation methodologies leading to the synthesis of various trisubstituted alkenes, carbocycles, heterocycles, natural products and biologically active molecules, have been well documented in the literature. This thesis de
650__|aPhysical and Basic Sciences|2AIU
653__|aChemistry
700__|aBasavaiah, D|eGuide
856__|uhttp://shodhganga.inflibnet.ac.in/handle/10603/1695|yShodhganga
905__|afromsg

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