H2O

C#CCC1C(=O)N(C)OC1c1ccccc1
Reaction #907
2-methyl-5-phenyl-4-propargylisoxazolin-3-one
収率 34.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CON=Cc1[nH]ccc1S(=O)(=O)NC(C)(C)C
Reaction #917
title compound
収率 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccn(C)c1S(=O)(=O)NC(=O)NC1=NC(OC)=CN(C)N1
Reaction #925
oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CC(=NO)C(=NO)C[C@]4(C)[C@H]3CC[C@]12C
Reaction #928
17β-Acetoxy-2,3-dihydroxyimino-5α-androstane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1c(Sc2ccccc2)cccc1[N+](=O)[O-]
Reaction #929
2-nitro-6-(phenylthio)benzonitrile
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1c(N)cccc1Sc1ccccc1
Reaction #930
2-Amino-6-(phenylthio)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(Sc2cccc([N+](=O)[O-])c2C#N)c1
Reaction #931
2-[(3,5-dimethylphenyl)thio]-6-nitrobenzonitrile
収率 73011.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(Sc2cccc(N)c2C#N)c1
Reaction #932
2-amino-6-[(3,5-dimethylphenyl)thio]benzonitrile
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(S(=O)(=O)c2cccc(F)c2C#N)c1
Reaction #933
2-Fluoro-6-[(3 -methoxyphenyl)sulfonyl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(S(=O)c2cccc(F)c2C#N)c1
Reaction #935
2-Fluoro-6-[(3-methoxyphenyl)sulfinyl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(S(=O)c2cccc(F)c2C#N)c1
Reaction #937
2-[(3,5-dimethylphenyl)sulfinyl]-6-fluorobenzonitrile
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(S(=O)(=O)c2cccc(F)c2C#N)c1
Reaction #938
2-[(3,5-dimethylphenyl)sulfonyl]-6-fluorobenzonitrile
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C)cc(Sc2cccc(F)c2C#N)c1
Reaction #941
2-Fluoro-6-[(3 -methyl-5-methoxyphenyl)thio]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(CN=[N+]=[N-])cc1
Reaction #951
4-cyanobenzyl azide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
[N-]=[N+]=NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1
Reaction #952
4-(benzyloxycarbonylamidino) benzyl azide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
[N-]=[N+]=NCCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #956
4-Azidoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)CC1
Reaction #957
4-Aminoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
[N-]=[N+]=NCC1CCN(C(=N)NC(=O)OCc2ccccc2)C1
Reaction #960
product
収率 68.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#CCC1CCN(Cc2ccccc2)C1
Reaction #962
product
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NCCC1CCN(Cc2ccccc2)C1
Reaction #963
product
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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