SYNTHESIS OF 3-METHYL 2-(Tert-utyldimethylsiloxy) FURAN B. Y. Makama
| dc.contributor.author | B. Y, Makama. | |
| dc.date.accessioned | 2023-12-14T06:53:52Z | |
| dc.date.available | 2023-12-14T06:53:52Z | |
| dc.date.issued | 2011-07-05 | |
| dc.description.abstract | Protection of 3-mcthyl-2-(5H)-furanone to 3-niethyl 2-(Tert-butyldimethyIsiloxy)furan was accomplished with an excellent yield of78%, which provided a neiu possible route for synthesizing \Y-butenolides. This concise method that started with abromobutyrolactone could lead to key methodologies towards the synthesis of fused bicycl cilac tones compou n ds | en_US |
| dc.identifier.citation | Andricux, J.; Barton, H. R.; Partin, H. J. 1977. Rhodiumcatalysed isomerisation of some unsaturated organic substrates. J. Chem. Soc., Perkin Trans, 1:359-363. Amarego, W. L. F.; Perrin, D. D. 1998. Purification of Laboratory Chemicals, Pergamon Press Oxford. Feringa, B. L.; De Lange Bolhuis, B. V. 1989. Asymmetric 1, 4-additions to 5-alkoxy-2 (5H)- furanonesenantioselectlve synthesis and absolute configuration determination of □- amino-Q-butyrolactones and amino diols. Tetrahedron, 45:6799 - 6818. | en_US |
| dc.identifier.uri | https://keffi.nsuk.edu.ng/handle/20.500.14448/5512 | |
| dc.language.iso | en | en_US |
| dc.publisher | Department of Chemistry, Nasarawa State University Keffi | en_US |
| dc.subject | 3-methyl-2-(5 H)-fura none, 3-methyl 2-(tert-butyldimethylsiloxy)furan, | Y-bu tenolides | en_US |
| dc.title | SYNTHESIS OF 3-METHYL 2-(Tert-utyldimethylsiloxy) FURAN B. Y. Makama | en_US |
| dc.type | Article | en_US |