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CC(C=CC1=C(C)CCCC1(C)C)=CC=CC(C)=CC=C(C)CSc1ccccc1
Reaction #3994
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Sc2ccccc2)ccc1[N+](=O)[O-]
Reaction #52205
2-amino-3-nitro-6-(phenylmercapto)pyridine
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C=CC1=C(C)CCCC1(C)C)=CC=CC(C)=CC=C(C)CSc1ccccc1
Reaction #93742
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CSc2ccccc2)cc1
Reaction #165419
title compound
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(Sc2ccccc2)c1
Reaction #175919
DOI: 10.1039/C8SC04228D
O=c1ccc(Sc2ccccc2)c[nH]1
Reaction #195714
DOI: 10.1039/C8SC04228D
Nc1c([N+](=O)[O-])ccc(Sc2ccccc2)c1Cl
Reaction #199524
DOI: 10.1039/C8SC04228D
COc1ccc(Sc2ccccc2)c([N+](=O)[O-])c1
Reaction #200432
DOI: 10.1039/C8SC04228D
Nc1nc2ccccc2c2c1ncn2CCSc1ccccc1
Reaction #212696
DOI: 10.1039/C8SC04228D
c1ccc(Sc2nccs2)cc1
Reaction #233196
DOI: 10.1039/C8SC04228D
c1ccc(Sc2nccs2)cc1
Reaction #242816
DOI: 10.1039/C8SC04228D
O=C1CCCc2cc(Sc3ccccc3)cc(F)c21
Reaction #253074
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(CSc2ccccc2)cc1
Reaction #291076
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(-c2ccccc2Sc2ccccc2-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #318925
4-Nitrophenylphenyl Sulfide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(Sc2ccccc2)c([N+](=O)[O-])c1
Reaction #379546
DOI: 10.1039/C8SC04228D
Cc1ccc(Sc2ccccc2)c([N+](=O)[O-])c1
Reaction #390760
DOI: 10.1039/C8SC04228D
O=C1CCCc2cc(Sc3ccccc3)cc(F)c21
Reaction #426375
8-Fluoro-6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one
DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1CC2=CC(=O)CC[C@@H]2[C@H]2CC[C@]3(C)[C@@H](OC(C)=O)CC[C@H]3[C@@H]21
Reaction #440885
(7α,17β)-17-(acetyloxy)-7-ethenylestr-4-en-3-one
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc(Sc2ccccc2)c[nH]1
Reaction #459915
5-(Phenylthio)-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCc2cc(Sc3ccccc3)cc(F)c21
Reaction #507384
8-Fluoro-6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one
DOI: 10.6084/m9.figshare.5104873.v1
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