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DC Field | Value | Language |
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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 |
Appears in Collections: | Student Theses (NCU) |
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9480.pdf Restricted Access | 25.5 MB | Adobe PDF | View/Open Request a copy |
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