A novel hydride rearrangement of the acetal group of tetraacetal tetraoxa-cages mediated by Lewis acids
| dc.citation.epage | 548 | en_US |
| dc.citation.issue | 6 | en_US |
| dc.citation.spage | 547 | en_US |
| dc.citation.volume | en_US | |
| dc.contributor.author | Wu, HJ | en_US |
| dc.contributor.author | Chern, JH | en_US |
| dc.contributor.department | 交大名義發表 | zh_TW |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | National Chiao Tung University | en_US |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:01:55Z | |
| dc.date.available | 2014-12-08T15:01:55Z | |
| dc.date.issued | 1997-03-21 | en_US |
| dc.description.abstract | Treatment of tetraoxa-cages 1a-f with Lewis acids such as TlC4, AlCl3, BF3 . OEt(2) and MeSO(3)H in dichloromethane at 25 degrees C gives the rearrangement products 2a-f in 90% yields regioselectively and stereoselectively; a novel hydride rearrangement of the acetal group of tetraacetal tetraoxa-cages mediated by Lewis acids. | en_US |
| dc.identifier.doi | 10.1039/a607403k | en_US |
| dc.identifier.issn | 1359-7345 | en_US |
| dc.identifier.journal | CHEMICAL COMMUNICATIONS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1039/a607403k | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/662 | |
| dc.language.iso | en_US | en_US |
| dc.title | A novel hydride rearrangement of the acetal group of tetraacetal tetraoxa-cages mediated by Lewis acids | en_US |
| dc.type | Article | en_US |