Busqueda de Subestructura

SCc1ccc(Cl)cc1

C=CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccccc21
Reaction #5920
2-(4-chlorophenyl)-4-acryloyl-3,4-dihyro-2H-1,4-benzothiazine
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccccc21.Cl
Reaction #5921
2-(4-chlorophenyl)-4-(dimethylamino)acetyl-3,4-dihydro-2H-1,4-benzothiazine hydrochloride
Rendimiento 165.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccccc21.O=C(O)C(=O)O
Reaction #5922
4-(N-allyl-N-methylaminoacetyl)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine oxalate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)N1CC(c2ccc(Cl)cc2)Sc2ccccc21
Reaction #5923
4-(4-bromobutyryl)-2-(4-chlorophenyl)-3,4-dihyro-2H-1,4-benzothiazine
Rendimiento 93.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2c(ccc3ccccc23)SC1c1ccc(Cl)cc1
Reaction #5924
3-(4-chlorophenyl)-1H-naphtho-[2,1-b][1,4]thiazin-2(3H)-one
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2CNc3c(ccc4ccccc34)S2)cc1
Reaction #5927
3-(4-chlorophenyl)-2,3-dihydro-1H-naphtho[2,1-b][1,4]thiazine
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccc3ccccc3c21
Reaction #5928
3-(4-chlorophenyl)-1-propenoyl-2,3-dihydro-1H-naphtho[2,1-b][1,4]thiazine
Rendimiento 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(c2ccc(Cl)cc2)Sc2ccc3ccccc3c2N1CCCCl
Reaction #5931
3-(4-chlorophenyl)-1-(3-chloropropyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one
Rendimiento 65.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CCCN1C(=O)C(c2ccc(Cl)cc2)Sc2ccc3ccccc3c21
Reaction #5933
1-[3-(N-allyl-N-methylamino)propyl]-3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@@H]1CCCN1S(=O)(=O)c1ccc2ccccc2c1)N1C[C@@H](c2ccc(Cl)cc2)Sc2ccccc21
Reaction #5934
(R)-2-(4-chlorophenyl)-4-[(S)-N-(2-naphthalenesulfonyl)prolyl]-3,4-dihydro-2H-1,4-benzothiazine
Rendimiento 51.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc([C@@H]2CNc3ccccc3S2)cc1
Reaction #5935
(R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine
Rendimiento 58.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)N1C[C@@H](c2ccc(Cl)cc2)Sc2ccccc21
Reaction #5936
(R)-4-chloroacetyl-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine
Rendimiento 108.8%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc([C@@H]2CNc3c(ccc4ccccc34)S2)cc1
Reaction #5937
(R)-(+)-3-(4-chlorophenyl)- 2,3-dihydro-1H-naphtho[2,1-b][1,4]thiazine
Rendimiento 63.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Cl)cc2SC1c1ccc(Cl)cc1
Reaction #5939
7-chloro-2-(4-chlorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C[S+](Cc2ccc(Cl)cc2)c2ccc(Cl)cc2)cc1.F[B-](F)(F)F
Reaction #6384
4-chlorophenylbis(4-chlorobenzyl)sulfonium tetrafluoroborate
Rendimiento 77.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Clc1ccc(CSC2=N[C@@H](c3ccccc3)[C@@H](c3ccccc3)N2)cc1Cl
Reaction #47034
product 204
Rendimiento 61.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccc(Cl)c(Cl)c1Cl)S(=O)(=O)O.NC[C@H](S)CC(=O)O
Reaction #50012
(3R)-4-amino--3-mercaptobutyric acid (-)-1-(2,3,4-trichlorophenyl)ethanesulfonate
Rendimiento 81.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CSCc1ccc(Cl)cc1
Reaction #55075
methyl p-chlorobenzylmercapto-acetate
Rendimiento 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CSCc1ccc(Cl)cc1)NO
Reaction #55076
p-Chlorobenzylmercapto-acetohydroxamic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CSCc1ccc(Cl)cc1
Reaction #56443
methyl p-chlorobenzylmercapto-acetate
Rendimiento 100.0%DOI: 10.6084/m9.figshare.5104873.v1
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