thiosalicylic acid

NS(=O)(=O)c1ccc(NC(=O)c2ccccc2SSc2ccccc2C(=O)O)cc1
Reaction #3838
title compound
收率 95.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(OCc1ccccc1)c1ccccc1SCc1ccccc1
Reaction #11404
2-Benzylsulfanyl Benzoic Acid Benzyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=c1c2ccccc2sc2ccc(O)cc12
Reaction #69390
2-hydroxy-thioxanthen-9-on
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=c1c2ccccc2sc2ccc(O)cc12
Reaction #71013
2-hydroxy-thioxanthen-9-on
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Sc1ccccc1C1=NCCN1
Reaction #75562
pure product
收率 53.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)c1ccccc1SC=Cc1ccccc1
Reaction #76601
2-styrylsulfanylbenzoic acid
收率 102.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=c1c2ccccc2sc2cc(O)cc(O)c12
Reaction #170279
compound
收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(OC)cc(Sc2ccccc2C(=O)O)c1
Reaction #177202
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CN1C(=O)c2cccc3c(Sc4ccccc4C(=O)O)ccc(c23)C1=O
Reaction #213867
title compound
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=C(Sc1ccccc1C(=O)O)c1ccccc1
Reaction #232271
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)Sc1ccccc1C(=O)O
Reaction #241281
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)Nc1ccc(C(=O)Sc2ccccc2C(=O)O)cc1
Reaction #242985
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1ccccc1SC(=O)C1CCC1
Reaction #243534
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1ccccc1SC1CCOC1=O
Reaction #244538
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(OC)cc(Sc2ccccc2C(=O)O)c1
Reaction #270579
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)c1ccccc1SCCCCl
Reaction #274419
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc2c(NS(C)(=O)=O)cccc2n1CC(=O)O
Reaction #277412
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(CC)C(=O)c1ccc([C@H](c2cccc(O)c2)N2C[C@@H](C)NC[C@@H]2C)cc1
Reaction #325076
4-[(R)-((2S,5R)-2,5-dimethyl-1-piperazinyl)-(3-hydroxyphenyl)methyl]-N,N-diethylbenzamide
收率 103.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=S(=O)(Nc1ccc([C@@H]2CCNC2)cc1)c1cccc(C(F)(F)F)c1
Reaction #326174
product
收率 3.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1ccc(-n2c(-c3c(C)noc3C)cc3ccccc32)cc1
Reaction #328804
4-(1-(4-methoxyphenyl)-1H-indol-2-yl)-3,5-dimethylisoxazole
收率 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
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