Recherche de Sous-structure

2654

S=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #1608
6-(4-chlorophenyl)-pyridazinthione
Rendement 187.1%DOI: 10.6084/m9.figshare.5104873.v1
S=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #1676
6-(4-chlorophenyl)-pyridazinthione
Rendement 187.1%DOI: 10.6084/m9.figshare.5104873.v1
S=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #2181
6-(4-chlorophenyl)-pyridazinthione
Rendement 187.1%DOI: 10.6084/m9.figshare.5104873.v1
S=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #2222
6-(4-chlorophenyl)-pyridazinthione
Rendement 187.1%DOI: 10.6084/m9.figshare.5104873.v1
S=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #2280
6-(4-chlorophenyl)-pyridazinthione
Rendement 187.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=S)c2ccc(N(C)C)cc2)cc1
Reaction #4699
4-dimethylamino-N-(4'-methoxyphenyl)-benzenecarbothiamide
Rendement 63.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2ccccc2C1=S
Reaction #4900
2-(2-Chloroethyl)-2,3-dihydro-4-methyl-1,4-benzoxazepine-5(4H)-thione
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2ncccc2C1=S
Reaction #4901
2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-thione
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2cc3ccccc3cc2C1=S
Reaction #4902
2-(2-Chloroethyl)-2,3-dihydro-4-methylnaphth[2,3-f][1,4]oxazepine-5(4H)-thione
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2cc(Cl)ccc2C1=S
Reaction #4903
orange oil
Rendement 73.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2ccc(Br)cc2C1=S
Reaction #4904
yellow solid
Rendement 72.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2c(ccc3ccccc23)C1=S
Reaction #4905
yellow crystals
Rendement 84.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2ccc(Cl)cc2C1=S
Reaction #4906
product
Rendement 86.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(=S)N(C)CC(CCCl)O2
Reaction #4907
product
Rendement 86.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2cc3ccccc3nc2C1=S
Reaction #4916
yellow crystals
Rendement 86.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2ccc([N+](=O)[O-])cc2C1=S
Reaction #4920
yellow crystals
Rendement 173.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2ccc(F)cc2C1=S
Reaction #4921
yellow crystals
Rendement 125.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccccc2nc1S
Reaction #5913
2-mercapto-3-methylquinoxaline
DOI: 10.6084/m9.figshare.5104873.v1
S=CN[C@@H]1CCCN2c3cc(Cl)ccc3Oc3ccccc3[C@H]12
Reaction #44434
trans-N-(7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)methanethioamide
Rendement 81.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](n2c(=O)sc3c(=S)[nH]c(N)nc32)[C@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #47759
77
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
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