部分構造検索

36459

Cc1ccc(C[S+](Cc2ccc(C)cc2)Cc2ccc(C)cc2)cc1.[F][Sb-]([F])([F])([F])([F])[F]
Reaction #6381
tris(p-methylbenzyl)sulfonium hexafluoroantimonate
収率 87.3%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Cl)c1CSCc1c(Cl)cccc1Cl
Reaction #6382
bis(2,6-dichlorobenzyl) sulfide
収率 80.4%DOI: 10.6084/m9.figshare.5104873.v1
CC[S+](Cc1cccc2ccccc12)Cc1cccc2ccccc12.[F][Sb-]([F])([F])([F])([F])[F]
Reaction #6385
bis(1-naphthylmethyl)ethylsulfonium hexafluoroantimonate
収率 98.5%DOI: 10.6084/m9.figshare.5104873.v1
Br.N=C(SCc1ccccc1)c1ccccc1
Reaction #9023
S-benzylthiobenzimidate hydrobromide
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(/C=C/c2c(OC)cc(OC)cc2OC)S(=O)(=O)C(/C=C/c2c(OC)cc(OC)cc2OC)c2ccc(OC)cc2)cc1
Reaction #47717
(E)-2,4,6-trimethoxystyryl-4-methoxybenzyl sulfone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(OC)c(-c2ccc(C(F)(F)F)cc2CSCc2ccccc2)c1
Reaction #66967
(2′-Benzylsulfanylmethyl-6-methoxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(SCc2ccccc2)=CCC3(C)C)cc1
Reaction #81676
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC=C(SCc2ccccc2)c2cc(C#Cc3ccc(C(=O)O)cc3)ccc21
Reaction #81677
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)C(F)(F)c1ccc(CSCc2ccccc2)cc1Br
Reaction #178222
DOI: 10.1039/C8SC04228D
C=CCOc1c(OC)cc(C2SCC(c3cc(OC)c(OC)c(OC)c3)S2)cc1[N+](=O)[O-]
Reaction #183426
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCCCC1(c2ccccc2)SC(c2cc(F)ccc2F)=NN1c1nnc(Br)s1
Reaction #187359
DOI: 10.1039/C8SC04228D
CN(O)C(=O)N1N=C(c2cc(F)ccc2F)SC1(CCCN)c1ccccc1
Reaction #188513
DOI: 10.1039/C8SC04228D
NC(=O)c1cccc(COc2ccccc2C2SC(c3ccc(F)cc3)=NN2C(=O)c2c(F)cc(F)cc2F)c1
Reaction #189257
DOI: 10.1039/C8SC04228D
CN(OC(C)(C)C)C(=O)N1N=C(c2cc(F)ccc2F)SC1(CCCN=[N+]=[N-])c1ccccc1
Reaction #189901
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](OCCC1(c2ccccc2)SC(c2cc(F)ccc2F)=NN1C(=S)NC(=O)c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #200122
DOI: 10.1039/C8SC04228D
CC(C)(C)C(=O)N1N=C(c2cc(F)ccc2F)SC1(CCCN=[N+]=[N-])c1ccccc1
Reaction #201343
DOI: 10.1039/C8SC04228D
CC(=O)N1CCC2(CC1)SC(c1ccccc1)c1ccccc12
Reaction #208319
DOI: 10.1039/C8SC04228D
CCC(C)c1cc(OC)cc2c1C(=O)N(CSc1ccccc1)S2(=O)=O
Reaction #216235
2-phenylthiomethyl-4-sec-butyl-6-methoxysaccharin
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(C(c1cc(-c2c[nH]nc2C(F)(F)F)ccc1C(F)F)C(F)(F)F)C(c1cc(-c2c[nH]nc2C(F)(F)F)ccc1C(F)F)C(F)(F)F
Reaction #227750
DOI: 10.1039/C8SC04228D
COC(=O)CSC(SCc1ccc(Cl)cc1)c1ccc(OCc2ccc3ccccc3n2)cc1
Reaction #227955
DOI: 10.1039/C8SC04228D
1 ページ次のページ