| dc.contributor.advisor | Chandrasekaran, S | |
| dc.contributor.author | Ramesha, A R | |
| dc.date.accessioned | 2005-04-27T06:03:31Z | |
| dc.date.accessioned | 2018-07-30T15:13:01Z | |
| dc.date.available | 2005-04-27T06:03:31Z | |
| dc.date.available | 2018-07-30T15:13:01Z | |
| dc.date.issued | 2005-04-27T06:03:31Z | |
| dc.date.submitted | 1994 | |
| dc.identifier.uri | https://etd.iisc.ac.in/handle/2005/107 | |
| dc.identifier.srno | null | |
| dc.description.abstract | Recent years have seen a dramatic expansion in synthetic and structural molybdenum - sulfur chemistry. The amplest binary Mo-S moiety in MO$ ion. The thromolybdates derived by sulfur substitution from the 0x0 analogue have interesting chemical properties. Although they have been studied extensively by synthetic inorganic chemists and bio-inorganic chemists as models for enzymes like introgenases, their reactivity towards organic substrates remamed unexplored. | en |
| dc.format.extent | 4493996 bytes | |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | en | |
| dc.publisher | Indian Institute of Science | en |
| dc.rights | I grant Indian Institute of Science the right to archive and to make available my thesis or dissertation in whole or in part in all forms of media, now hereafter known. I retain all proprietary rights, such as patent rights. I also retain the right to use in future works (such as articles or books) all or part of this thesis or dissertation. | en |
| dc.subject.classification | Organic Chemistry | en |
| dc.subject.keyword | Organic Synthesis Sulfonation Reactions | en |
| dc.title | Organosulfur Reactions In Organic Synthesis With Tetrathiomolybdate | en |
| dc.type | Electronic Thesis and Dissertation | en |
| dc.degree.name | PhD | en |
| dc.degree.level | Doctoral | en |
| dc.degree.grantor | Indian Institute of Science | en |
| dc.degree.discipline | Faculty of Science | en |
