1-ETHYLPIPERIDINE HYPOPHOSPHITE
1-ETHYLPIPERIDINE HYPOPHOSPHITE structure
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Common Name | 1-ETHYLPIPERIDINE HYPOPHOSPHITE | ||
|---|---|---|---|---|
| CAS Number | 145060-63-5 | Molecular Weight | 179.19700 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C7H18NO2P | Melting Point | 40-43 ℃(lit.) | |
| MSDS | Chinese USA | Flash Point | 132.8 °F | |
| Symbol |
GHS02, GHS07 |
Signal Word | Danger | |
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Hydrolysis-Sensitive Dithiolethione Prodrug Micelles.
Macromol. Biosci. 15 , 1512-22, (2015) Prodrug micelles carrying 5-(4-hydroxyphenyl)-3H-1,2-dithiole-3-thione (ADT-OH), a compound possessing chemopreventive properties, are prepared from amphiphilic block copolymers linking ADT-OH via an ester bond using glycine (PAM-PGlyADT) and isoleucine linke... |
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A novel and efficient methodology for the C-C bond forming radical cyclization of hydrophobic substrates in water.
Org. Lett. 3(8) , 1157-60, (2001) [reaction: see text]. The combination of water-soluble radical initiator 2,2'-azobis[2-(2-imidazolin-2-yl)propane] (VA-061), water-soluble chain carrier 1-ethylpiperidine hypophosphite (EPHP), and surfactant cetyltrimethylammonium bromide (CTAB) was found to ... |
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Hypophosphite mediated carbon-carbon bond formation: total synthesis of epialboatrin and structural revision of alboatrin. Graham SR, et al.
J. Chem. Soc. Perkin Trans. I 21 , 3071-73, (1999)
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Tributyltin hydride and 1-ethylpiperidine hypophosphite mediated intermolecular radical additions to 2, 4, 6-trichlorophenyl vinyl sulfonate. Edetanlen-Elliot O, et al.
Tetrahedron Lett. 48(50) , 8926-29, (2007)
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Hypophosphite mediated carbon-carbon bond formation: A clean approach to radical methodology. Graham SR, et al.
Tetrahedron Lett. 40(!2) , 2415-16, (1999)
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Chemoselective 1-ethylpiperidine hypophosphite (EPHP)-mediated intermolecular radical additions of 1-deoxy-1-halo-1-iodo-alditols to electron-deficient olefins. Francisco CG, et al.
Tetrahedron Lett. 47(51) , 9057-60, (2006)
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Stereoselective synthesis of trisubstituted tetrahydrofurans by radical cyclisation reaction using a hypophosphite salt. Application to the total synthesis of (±)-dihydrosesamin. Roy SC, et al.
Tetrahedron 58(12) , 2435-39, (2002)
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