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dc.contributor.advisorIla, H.-
dc.contributor.authorAcharya, Anand-
dc.date.accessioned2019-07-18T11:07:50Z-
dc.date.available2019-07-18T11:07:50Z-
dc.date.issued2018-01-29-
dc.identifier.citationAcharya, Anand. 2018, New synthetic strategies for five membered heterocycles via novel organosulfur synthons, Ph.D thesis, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluruen_US
dc.identifier.urihttps://libjncir.jncasr.ac.in/xmlui/handle/10572/2640-
dc.description.abstractFor 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.isoEnglishen_US
dc.publisherJawaharlal Nehru Centre for Advanced Scientific Researchen_US
dc.rights© 2018 JNCASR-
dc.subjectHeterocyclic compounds synthesisen_US
dc.subjectOrganosulfur synthonsen_US
dc.titleNew synthetic strategies for five membered heterocycles via novel organosulfur synthonsen_US
dc.typeThesisen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePh.D.en_US
dc.publisher.departmentNew Chemistry Unit (NCU)en_US
Appears in Collections:Student Theses (NCU)

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