ethyl-2-azidoacetate

CCOC(=O)/C(=C/C=C/c1ccc(C)cc1)N=[N+]=[N-]
Reaction #40813
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)/C(=C/C=C/c1ccc(C(C)C)cc1)N=[N+]=[N-]
Reaction #40852
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(N=[N+]=[N-])C(O)c1cccnc1Cl
Reaction #83798
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)Cn1nncc1-c1ccc2c(c1)ncn2-c1cc(NC(C)=O)cc(-c2ccc(F)cc2F)c1
Reaction #92470
Ethyl 2-(5-(1-(5-acetamido-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)-1H-benzo[d]-imidazol-5-yl)-1H-1,2,3-triazol-1-yl)acetate
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)Cn1nnnc1Cl
Reaction #95979
ethyl 5-chloro-1H-tetrazol-1-ylacetate
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)C(=Cc1ccc(Br)s1)N=[N+]=[N-]
Reaction #164614
acrylate
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cn1cc(-c2cccc(O)c2)nn1
Reaction #169494
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cn1cc(C2(O)CCCC2)nn1
Reaction #169496
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(=Cc1ccc(-c2ccccc2)s1)N=[N+]=[N-]
Reaction #177076
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(=Cc1cc(C)cc(C)c1)N=[N+]=[N-]
Reaction #212064
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(=Cc1cncn1-c1ccc(Br)cc1)N=[N+]=[N-]
Reaction #240095
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(=Cc1cccs1)N=[N+]=[N-]
Reaction #248152
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(=CC=Cc1c(OC)cccc1OC)N=[N+]=[N-]
Reaction #249936
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(=CC=Cc1ccc(C)cc1)N=[N+]=[N-]
Reaction #262012
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C(=Cc1cccc(F)c1C)N=[N+]=[N-]
Reaction #262115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C(=Cc1ccccc1OC)N=[N+]=[N-]
Reaction #264491
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C(=Cc1cccc([Si](C)(C)C)c1)N=[N+]=[N-]
Reaction #270025
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)Cn1cc(C#N)nn1
Reaction #329441
(4-Cyano-1H-1,2,3-triazol-1-yl)acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(=O)C(=Cc1ccc(C(O)P(=O)(OC(C)(C)C)OC(C)(C)C)cc1)N=[N+]=[N-]
Reaction #345348
7
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
C=C(N=[N+]=[N-])C(=O)OCC
Reaction #407348
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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