sheldxt sofware suite v. 6.0 (Bruker Corporation)
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90
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Bruker Corporation
sheldxt sofware suite v. 6.0
Sheldxt Sofware Suite V. 6.0, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sheldxt+sofware+suite+v%2E+6%2E0/sheldxt+sofware+suite+v++6+0/10__1016_slash_j__jfluchem__2009__06__011-295-1-9
Average 90 stars, based on 1 article reviews
Sheldxt Sofware Suite V. 6.0, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sheldxt+sofware+suite+v%2E+6%2E0/sheldxt+sofware+suite+v++6+0/10__1016_slash_j__jfluchem__2009__06__011-295-1-9
Average 90 stars, based on 1 article reviews
sheldxt sofware suite v. 6.0 - by Bioz Stars,
2026-11
90/100 stars
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other:Article Title: Reactions of polyfluorinated thietanes Article Snippet: Oxidation of 4-substituted 2,2-bis(trifluoromethyl)thietanes by m-chloroperoxybenzoic acid results in selective formation of the corresponding S-oxides in 65–86% yield.. Oxidation of 4-C2H5S-2,2bis(trifluoromethyl)thietane under mild conditions led to selective formation of 4-C2H5SO2-2,2bis(trifluoromethyl)thietane, which under more rigorous conditions was selectively converted into trans-4-C2H5SO2-2,2-bis(trifluoromethyl)thietane-1-S-oxide.. Reaction of 4-substituted 2,2-bis(trifluoromethyl)thietanes with activated aluminum powder results in a highly selective ring expansion process, producing the corresponding 5-fluoro-4-(trifluoromethyl)-2,3-dihydro-2-alkoxythiophenes in 58–93% yield. |