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New synthetic strategies for five membered heterocycles via novel organosulfur synthons

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dc.contributor.advisor Ila, H.
dc.contributor.author Acharya, Anand
dc.date.accessioned 2019-07-18T11:07:50Z
dc.date.available 2019-07-18T11:07:50Z
dc.date.issued 2018-01-29
dc.identifier.citation Acharya, Anand. 2018, New synthetic strategies for five membered heterocycles via novel organosulfur synthons, Ph.D thesis, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru en_US
dc.identifier.uri https://libjncir.jncasr.ac.in/xmlui/handle/10572/2640
dc.description.abstract For several years, our research group has been involved in design and development of novel organosulfur building blocks and their synthetic applications for construction of substituted and fused five/six membered heterocycles. In this chapter, a brief account of these intermediates has been given. 1.1 Polarized Ketene Dithioacetals The versatile synthon family of polarized ketene dithioacetals of the general structure A has been proven to be among the simplest and useful synthetic building blocks in various organic transformations.1 Among them, the corresponding α-oxoketene dithioacetals have been extensively studied by our research group.1a-b These organosulfur synthons can easily be prepared by the reaction of CS2 with various active methylene ketones in the presence of base followed by alkylation in one-pot reaction (Scheme 1). en_US
dc.language.iso English en_US
dc.publisher Jawaharlal Nehru Centre for Advanced Scientific Research en_US
dc.rights © 2018 JNCASR
dc.subject Heterocyclic compounds synthesis en_US
dc.subject Organosulfur synthons en_US
dc.title New synthetic strategies for five membered heterocycles via novel organosulfur synthons en_US
dc.type Thesis en_US
dc.type.qualificationlevel Doctoral en_US
dc.type.qualificationname Ph.D. en_US
dc.publisher.department New Chemistry Unit (NCU) en_US


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  • Student Theses (NCU) [133]
    MS and PhD theses from New Chemistry Unit are submitted to this collection.

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