An 31 Reaktionen beteiligt

1429378

O=[N+]([O-])c1c(CS(=O)(=O)c2cccc3ccccc23)cccc1OC(CCl)CCl
Reaction #61385
title compound
Ausbeute 66.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=[N+]([O-])c1ccc(F)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #185720
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OCc1ccccc1)N1CCC(COc2ccc([N+](=O)[O-])c(CS(=O)(=O)c3cccc4ccccc34)c2)CC1
Reaction #237526
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1ccc(OCCCCCl)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #252014
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1c(CS(=O)(=O)c2cccc3ccccc23)cccc1OC(CCl)CCl
Reaction #286993
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=[N+]([O-])c1ccc(OC2CCCN(Cc3ccccc3)C2)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #401511
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(CS(=O)(=O)c2cccc3ccccc23)c([N+](=O)[O-])c(OCCCl)c1
Reaction #406649
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=[N+]([O-])c1ccc(F)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #634440
1-(5-fluoro-2-nitrobenzyl-sulfonyl)naphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
O=[N+]([O-])c1c(CS(=O)(=O)c2cccc3ccccc23)cccc1OCCCCl
Reaction #773375
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=[N+]([O-])c1ccc(OC2CCN(Cc3ccccc3)CC2)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #905146
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=[N+]([O-])c1c(CS(=O)(=O)c2cccc3ccccc23)cccc1OCCCl
Reaction #925715
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=S(=O)(CCl)c1cccc2ccccc12
Reaction #1202769
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=[N+]([O-])c1ccc(OC2CCN(Cc3ccccc3)C2)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #1647697
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
O=S(=O)(CCl)c1cccc2ccccc12
Reaction #1798573
1-chloromethanesulfonyl-naphthalene
Ausbeute 88.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_09
O=[N+]([O-])c1ccc(OC2CCN(Cc3ccccc3)C2)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #1798575
1-benzyl-3-[3-(naphthalene-1-sulfonylmethyl)-4-nitro-phenoxy]-pyrrolidine
Ausbeute 47.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_09
O=[N+]([O-])c1ccc(OC2CCN(Cc3ccccc3)CC2)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #1798585
1-benzyl-4-[3-(naphthalene-1-sulfonylmethyl)-4-nitro-phenoxy]-piperidine
Ausbeute 47.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_09
O=C(OCc1ccccc1)N1CCC(COc2ccc([N+](=O)[O-])c(CS(=O)(=O)c3cccc4ccccc34)c2)CC1
Reaction #1798597
title compound
Ausbeute 74.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_09
O=[N+]([O-])c1ccc(OC2CCCN(Cc3ccccc3)C2)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #1798602
title compound
Ausbeute 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_09
O=[N+]([O-])c1ccc(F)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #2215690
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
O=[N+]([O-])c1ccc(F)cc1CS(=O)(=O)c1cccc2ccccc12
Reaction #2232922
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
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