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520749

COc1ccc(S(=O)(=O)NOC(C)C)cc1
Reaction #57428
N1-(isopropoxy)-4-methoxy-1-benzenesulfonamide
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1OC1CCCC1
Reaction #57429
2-(cyclopentyloxy)-1H-isoindole-1,3(2H)-dione
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)NOC2CCCC2)cc1
Reaction #57430
N1-(cyclopentyloxy)-4-methoxy-1-benzenesulfonamide
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(S(=O)(=O)NOC2CCCC2)cc1[N+](=O)[O-]
Reaction #57432
4-amino-N-(cyclopentyloxy)-3-nitrobenzenesulfonamide
Ausbeute 68.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(S(=O)(=O)NOC2CCCC2)c1
Reaction #57434
N1-(cyclopentyloxy)-3-nitro-1-benzenesulfonamide
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)ON1C(=O)c2ccccc2C1=O
Reaction #57436
yellow solid
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1OC1CCOCC1
Reaction #57440
2-(tetrahydro-2H-pyran-4-yloxy)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)NOC2CCOCC2)cc1
Reaction #57441
white solid
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)NOC2CCOC2)cc1
Reaction #57443
N-(tetrahydro-3-furanyloxy)-4-methoxy-1-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1OC1CCCCC1
Reaction #57446
2-(cyclohexyloxy)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)NOC2CCCCC2)cc1
Reaction #57447
white solid
Ausbeute 492.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1OC1CCCCC1
Reaction #57478
2-(cyclohexyloxy)-1H-isoindole-1,3(2H)-dione
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](ON)[C@@H](CO[Si](C)(C)C(C)(C)C)O2)c(=O)[nH]c1=O
Reaction #81372
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](ON3C(=O)c4ccccc4C3=O)[C@@H](CO[Si](C)(C)C(C)(C)C)O2)c(=O)[nH]c1=O
Reaction #82910
compound 2
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](ON)[C@@H](CO[Si](C)(C)C(C)(C)C)O2)c(=O)[nH]c1=O
Reaction #82911
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1OC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #170138
title compound
Ausbeute 37.3%DOI: 10.6084/m9.figshare.5104873.v1
NOC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #170139
title compound
Ausbeute 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(ON)CO1
Reaction #196941
DOI: 10.1039/C8SC04228D
O=CNc1nc(C(=NOC2C=CCCC2)C(=O)O)ns1
Reaction #197418
DOI: 10.1039/C8SC04228D
NOC1CCN(S(=O)(=O)c2cccc(C(F)(F)F)c2)CC1
Reaction #197529
DOI: 10.1039/C8SC04228D
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