PENTAFLUOROPHENYL CHLOROTHIONOFORMATE
PENTAFLUOROPHENYL CHLOROTHIONOFORMATE structure
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Common Name | PENTAFLUOROPHENYL CHLOROTHIONOFORMATE | ||
|---|---|---|---|---|
| CAS Number | 135192-53-9 | Molecular Weight | 262.58400 | |
| Density | 1.635 g/mL at 25ºC(lit.) | Boiling Point | 98-102ºC50 mm Hg(lit.) | |
| Molecular Formula | C7ClF5OS | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 189 °F | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Regioselective synthesis of beta-N1- and beta-N3-alloxazine nucleosides
Org. Lett. 2(2) , 227-30, (2000) [structures: see text] A regio- and stereoselective glycosylation of ribose tetraester with persilylated alloxazine to give either beta-N1 or beta-N3 nucleosides is described. The N3 product is potentially of interest as a fluorescent nucleoside and is predic... |
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Tuning the acceptors in catalyzed cyclizations initiated by allenes. Silylstannylation/cyclization of allene-aldehydes for synthesis of polyalkylated indolizidines including 223A congeners.
J. Org. Chem. 69(26) , 9151-8, (2004) Starting from succinamide and 1,2-heptadiene-4-ol, a racemic allene-aldehyde substrate, 20, suitable for R(3)SiSnR'(3)-mediated cyclization was synthesized in six steps and in 21% yield. Stereoselective cyclization (relative cis configuration at the new stere... |
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The invention of radical reactions. Part XXI. Simple methods for the radical deoxygenation of primary alcohols. Barton DHR, et al.
Tetrahedron 47(43) , 8969-94, (1991)
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