SYNTHESIS OF 3-METHYL 2-(Tert-utyldimethylsiloxy) FURAN B. Y. Makama

dc.contributor.authorB. Y, Makama.
dc.date.accessioned2023-12-14T06:53:52Z
dc.date.available2023-12-14T06:53:52Z
dc.date.issued2011-07-05
dc.description.abstractProtection 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 dsen_US
dc.identifier.citationAndricux, 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.urihttps://keffi.nsuk.edu.ng/handle/20.500.14448/5512
dc.language.isoenen_US
dc.publisherDepartment of Chemistry, Nasarawa State University Keffien_US
dc.subject3-methyl-2-(5 H)-fura none, 3-methyl 2-(tert-butyldimethylsiloxy)furan, | Y-bu tenolidesen_US
dc.titleSYNTHESIS OF 3-METHYL 2-(Tert-utyldimethylsiloxy) FURAN B. Y. Makamaen_US
dc.typeArticleen_US

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