(S)-(+)-Benzyl glycidyl ether
(S)-(+)-Benzyl glycidyl ether structure
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Common Name | (S)-(+)-Benzyl glycidyl ether | ||
|---|---|---|---|---|
| CAS Number | 16495-13-9 | Molecular Weight | 164.201 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 252.7±15.0 °C at 760 mmHg | |
| Molecular Formula | C10H12O2 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 100.9±19.9 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Bioresolution of benzyl glycidyl ether using whole cells of Bacillus alcalophilus.
J. Basic Microbiol. 52(4) , 383-9, (2012) The incubation of whole Bacillus alcalophilus cells grown on a mineral supplemented medium (MSM) containing 1% (w/v) sucrose as carbon source, 1.2% (w/v) tryptone as nitrogen source at pH 6.5 and temperature 30 °C in 24 h kinetically resolved benzyl glycidyl ... |
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Metal-mediated cyclization of aryl and benzyl glycidyl ethers: a complete scenario.
J. Am. Chem. Soc. 130(50) , 16838-9, (2008) Enantiomerically pure aryl and benzyl glycidyl ethers undergo stereospecific cyclizations leading to 3-chromanols or to tetrahydrobenzo[c]oxepin-4-ols under mild conditions in the presence of a catalytic amount of FeBr3/3AgOTf. The same processes are also med... |
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Enantioselective total synthesis of (+)-gigantecin: exploiting the asymmetric glycolate aldol reaction.
J. Am. Chem. Soc. 126(40) , 12790-1, (2004) The enantioselective synthesis of the potent, selective, cytotoxic, annonaceous acetogenin, (+)-gigantecin, has been completed. An asymmetric glycolate aldol serves to establish the stereocenters at C13,14 and at C21,22. A Carreira asymmetric acetylide additi... |
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