Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate
![Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate Structure](https://image.chemsrc.com/caspic/013/173459-80-8.png)
Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate structure
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Common Name | Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate | ||
|---|---|---|---|---|
| CAS Number | 173459-80-8 | Molecular Weight | 310.30700 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C16H14N4O3 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Benzotriazole-mediated syntheses of depsipeptides and oligoesters.
J. Org. Chem. 76 , 4884-4893, (2011) Reactions of O-Pg(α-hydroxyacyl)benzotriazoles with (a) unprotected α-hydroxycarboxylic acids, (b) amino acids, and (c) amines afforded, respectively, chirally pure (a) oligoesters, (b) depsidipeptides, and (c) amide conjugates (yields 52-94%). N-Pg(α-Aminoac... |
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Efficient preparation of aminoxyacyl amides, aminoxy hybrid peptides, and alpha-aminoxy peptides.
J. Org. Chem. 74th ed.,, 8690-8694, (2009) N-(Pg-alpha-aminoxy acids) 1a-g are converted to N-(Pg-alpha-aminoxyacyl)benzotriazoles 2a-g, which react under mild conditions with amines, alpha-amino acids/alpha-dipeptides, and alpha-aminoxy acids to give aminoxyacyl amides 3a-g, (3e+3e'), and (3g+3g'), a... |
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Abdelmajeid, A.; Tala, S. R.; Amine, M. S.; Katritzky, A. R.
Synthesis , 2995-3005, (2011)
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Hansen, F. K.; Beagle, L. K.; Todadze, E.; Katritzky, A. R.
Heterocycles 84th ed.,, 515-526, (2012)
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Katritzky, A. R.; Narindoshvili, T.; Angrish, P.
Synthesis , 2013-2022, (2008)
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Katritzky, A. R.; Angrish, P.; Todadze, E.
Synlett , 2392-2411, (2009)
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