| Type of Material: | Thesis |
| Title: | Prins type cascade cyclizat fused bridged and spiro tetrahydropyran tetrahyd cyclizations for the synthesis of tetrahydrofuran derivatives |
| Researcher: | Prudhvi Raju, N. |
| Guide: | Jagan Mohan Reddy, B. |
| Department: | Department of Chemistry |
| Publisher: | Adikavi Nannaya University |
| Place: | Rajahmundry |
| Year: | 2016 |
| Language: | English |
| Subject: | Chemical Science | Chemistry | Physical and Basic Sciences |
| Dissertation/Thesis Note: | PhD; Department of Chemistry, Adikavi Nannaya University, Rajahmundry; 2016 |
| Fulltext: | Shodhganga |
| 003 | IN-AhILN | |
| 005 | 2026-08-25 12:36:55 | |
| 008 | __ | 260825t2016||||ii#||||g|m||||||||||eng|| |
| 035 | __ | |a(IN-AhILN)th_462268 |
| 040 | __ | |dIN-AhILN|aANUR_533105 |
| 041 | __ | |aeng |
| 100 | __ | |eResearcher|aPrudhvi Raju, N. |
| 110 | __ | |aDepartment of Chemistry|0U-0005|dRajahmundry|bAdikavi Nannaya University|ein |
| 245 | __ | |aPrins type cascade cyclizat fused bridged and spiro tetrahydropyran tetrahyd cyclizations for the synthesis of tetrahydrofuran derivatives |
| 260 | __ | |aRajahmundry|c2016|bAdikavi Nannaya University |
| 300 | __ | |dDVD |
| 502 | __ | |d2016|bPhD|cDepartment of Chemistry, Adikavi Nannaya University, Rajahmundry |
| 518 | __ | |d2016|oDate of Award |
| 518 | __ | |oDate of Registration|d2011 |
| 518 | __ | |oDate of Completion|d2016 |
| 520 | __ | |aChapter I: Describes the general introduction about Prins type cascade cyclizations focusing new methodologies development and application to natural product synthesis, as a background that lead us to choose this reaction as key topic for our research. The brief review is discussed previous reports cited in the literature on development in this area for the stereoselective synthesis of wide range of tetrahydropyran and tetrahydrofuran derivatives, aim and objective of the research work. Chapter II: Describes the development of new synthetic methodologies for the stereo selective synthesis of 2, 3, 6 tri-substituted tetrahydropyrans and spiropyrolidine derivatives through Prins/Ene cyclization, which is further, divided into two sections. Section A: This section describes A simple and expeditious synthesis of 2, 3, 6-tri substituted tetrahydropyrans through Prins/Ene cyclization using molecular iodine. Section B: This section describes the domino Prins/Ene cyclization and Prins bicyclization for the synthesi |
| 650 | __ | |aChemistry|2UGC |
| 650 | __ | |aPhysical and Basic Sciences|2AIU |
| 653 | __ | |aChemical Science |
| 700 | __ | |aJagan Mohan Reddy, B.|eGuide |
| 856 | __ | |uhttp://shodhganga.inflibnet.ac.in/handle/10603/314810|yShodhganga |
| 905 | __ | |afromsg |
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