Recherche de Sous-structure

CSCCN

NCC(O)C[n+]1ccc(SCC2=C(C(=O)O)N3C(=O)[C@@H](NC(=O)CSc4cc(Cl)ccc4Cl)[C@H]3SC2)cc1.[Cl-]
Reaction #3762
title compound
Rendement 127.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(OS(=O)(=O)c3ccc(Br)cc3)CS[C@H]12
Reaction #5643
title compound
Rendement 54.1%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5644
title compound
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
Rendement 63.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(Oc2ccc(CC3SC(=O)NC3=O)cc2)cc1)NC(=O)C(N)Cc1c[nH]cn1.Cl.Cl
Reaction #7443
title compound
Rendement 163.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(Oc2ccc(CC3SC(=O)NC3=O)cc2)cc1)NC(=O)C(N)Cc1c[nH]cn1.Cl.Cl
Reaction #7444
title compound
Rendement 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(Oc2ccc(C=C3SC(=O)NC3=O)cc2)cc1)NC(=O)C1CCCN1C(=O)OC(C)(C)C
Reaction #7445
required product
Rendement 32.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(Oc2ccc(C=C3SC(=O)NC3=O)cc2)cc1)NC(=O)C(C)NC(=O)OC(C)(C)C
Reaction #7449
crude compound
Rendement 36.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1cc(N2CCSCC2)ncc1N(C)C(=O)C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #50925
title compound
Rendement 80.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1cc(N2CCS(=O)(=O)CC2)ncc1N(C)C(=O)C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #50926
title compound
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1NCCSC1S(=O)(=O)c1ccc(Oc2ccc(-c3ccoc3)cc2)cc1
Reaction #51451
4-(4-(furan-3-yl)phenoxy)benzenesulfonyl-tetrahydro-2H-1,4-thiazine-3-carboxylic acid
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1NCCSC1S(=O)(=O)c1ccc(Oc2ccc(-c3ccoc3)cc2)cc1
Reaction #51452
4-(4-(furan-3-yl)phenoxy)benzenesulfonyl-tetrahydro-2H-1,4-thiazine-3-carboxamide
Rendement 14.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N1Cc2cc(OC)ccc2SC(c2ccc(OC)cc2)C1
Reaction #64847
4-acryloyl-2-[4-methoxyphenyl]-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepine
Rendement 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CN(C(=O)CBr)Cc3cc(OC)ccc3S2)cc1
Reaction #64849
4-bromoacetyl-7-methoxy-2-(4-methoxyphenyl)-2,3,4,5-tetrahydro-1,4-benzothiazepine
Rendement 74.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(OS(=O)(=O)c3ccc(Br)cc3)CS[C@H]12
Reaction #65629
title compound
Rendement 54.1%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65630
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(C(=O)N2C[C@H](S(=O)(=O)c3ccccc3Cl)C[C@H]2C(=O)NC2(C#N)CC2)(c2ncc(Br)cc2F)C1
Reaction #156711
title compound
Rendement 40.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)SCCN(S(=O)(=O)c2ccc3ccccc3c2)C1C(=O)O
Reaction #164517
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCCC(O)CNc1ccc2c(c1)NC(=O)CS2
Reaction #186801
DOI: 10.1039/C8SC04228D
Clc1ccc(C2CNc3c(ccc4ccccc34)S2)cc1
Reaction #193231
DOI: 10.1039/C8SC04228D
Page 1Suivant