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http://hdl.handle.net/123456789/2766
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DC Field | Value | Language |
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dc.contributor.author | Bankar, S.K. | - |
dc.contributor.author | Shirke, R.P. | - |
dc.contributor.author | Ramasastry, S.S.V. | - |
dc.date.accessioned | 2020-12-07T10:33:12Z | - |
dc.date.available | 2020-12-07T10:33:12Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Advanced Synthesis and Catalysis, 357 (14-15) | en_US |
dc.identifier.other | 10.1002/adsc.201500505 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/full/10.1002/adsc.201500505 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2766 | - |
dc.description.abstract | An efficient diversity‐oriented approach for the synthesis of previously unknown di‐, tri‐, tetra‐ and spirocyclic pyrano‐1,4‐dioxinones, pyrano‐1,4‐dithiinones and pyrano‐1,4‐oxathiinones from readily available starting compounds has been described. Cascade Michael addition–cycloacetalisation of acetoxy‐, alkoxy‐, and aryloxypyranones and 1,2‐dinucleophiles under mild Lewis acidic conditions provides a direct access to oxygen and sulfur‐containing complex heterocycles. Mechanistic aspects of the cascade process were elucidated in light of experimental facts. The methodology described herein shows high promise for the synthesis of several bioactive natural products as well as pharmaceutically important compounds. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Wiley-VCH Verlag | en_US |
dc.subject | cascade reactions | en_US |
dc.subject | heterocycles | en_US |
dc.subject | Lewis acids | en_US |
dc.subject | natural products | en_US |
dc.subject | pyranones | en_US |
dc.title | Synthesis of O,S-Containing Polycycles via One-Pot Michael Addition-Cycloacetalisation Cascade | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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