Eschenmoser's reagent
Eschenmoser's reagent structure
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Common Name | Eschenmoser's reagent | ||
|---|---|---|---|---|
| CAS Number | 33797-51-2 | Molecular Weight | 185.007 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C3H8IN | Melting Point | 219 °C (dec.)(lit.) | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Total synthesis and bioactivity of an unnatural enantiomer of merrilactone a: development of an enantioselective desymmetrization strategy.
J. Org. Chem. 72 , 3065, (2007) (-)-Merrilactone A [(-)-1], isolated from Illicium merrillianum in 2000, possesses neurite outgrowth activity in cultures of fetal rat cortical neurons, and, therefore, is expected to show therapeutic potential for the treatment of neurodegeneration associate... |
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J. Prakt. Chem./Chem.-Ztg. 336 , 91, (1994)
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Chem. Abstr. 120 , 190555b, (1994)
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Tetrahedron Asymmetry 5 , 921, (1994)
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J. Chem. Soc. Perkin Trans. I , 3295, (1992)
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A new method using 2-chloro-4, 6-dimethoxy-1, 3, 5-triazine for facile elimination of dimethylamino group in Eschenmoser's methylenation for synthesis of a, ß-unsaturated esters. Yamada K, et al.
Tetrahedron Lett. 54(13) , 1753-60, (2013)
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Synthetic Routes to Unsymmetrical Porphyrins. Nardis S.
Synthesis and Modifications of Porphyrinoids , (2014), 203-39
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