Поиск подструктуры

CCCCOC(=O)CS

—
Reaction #46040
sulfuric acid ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SC2=C(O)CC(CCC3CCCO3)(C(C)C)OC2=O)c(C(C)(C)C)cc1CO
Reaction #51783
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SC2=C(O)CC(CCc3ccsc3)(C(C)C)OC2=O)c(C(C)(C)C)cc1CO
Reaction #51784
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc2ncsc2cc1SC1=C(O)CC(CCc2ccc(F)cc2)(C(C)C)OC1=O
Reaction #51789
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SC2=C(O)C[C@@](CCc3ccc(O)cc3)(C(C)C)OC2=O)c(C(C)C)c2sc(N)nc12
Reaction #51790
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1(CCc2ccccc2CO)CC(O)=C(Sc2sc3ccccc3c2C(C)(C)C)C(=O)O1
Reaction #51791
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1sc(CO)cc1SC1=C(O)CC(CCc2ccsc2)(C(C)C)OC1=O
Reaction #51792
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(OC(=O)CS(=O)(=O)C(C)(C)C)CC(C)(C)N1
Reaction #54461
2,2,6,6-tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCl
Reaction #81041
Lauryl-myristyl Chloroacetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC12CC3CC(CC(C3)C1)C2)C(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #172158
triphenylsulfonium (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonate
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[NH3+].O=C(OCC12CC3CC(CC(C3)C1)C2)C(F)(F)S(=O)(=O)[O-]
Reaction #172159
(adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid tert-butylammonium salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[NH3+].O=C(OCC12CC3CC(CC(C3)C1)C2)C(F)(F)S(=O)(=O)[O-]
Reaction #172160
(adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid tert-butylammonium salt
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC12CC3CC(CC(C3)C1)C2)C(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #172161
triphenylsulfonium (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonate
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCC2(C3CCCC3)CC(O)=C(Sc3nnc(CN(C)C)n3C)C(=O)O2)cc1Cl
Reaction #180732
DOI: 10.1039/C8SC04228D
Cc1cc(C)n2nc(SC3=C(O)CC(CCNC(=O)CCc4ccco4)(C4CCCC4)OC3=O)nc2n1
Reaction #185359
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(CCC(CC2CCCCC2)OC(=O)CSCC(=O)OCc2ccccc2)cc1NC(=O)CC1c2ccccc2Oc2ccccc21
Reaction #189588
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCC(S)C(=O)OCC1OC(n2cc(Br)c(=O)[nH]c2=O)C(O)(Cc2ccccc2)C1OCc1ccccc1
Reaction #190407
DOI: 10.1039/C8SC04228D
COc1cc(OC)c(CCC2(C3CCCC3)CC(O)=C(Sc3nc4nc(C)cc(C)n4n3)C(=O)O2)cc1Cl
Reaction #190898
DOI: 10.1039/C8SC04228D
COc1ccc(CCC2(C3CCCC3)CC(O)=C(Sc3nc(C)cc(C)c3C#N)C(=O)O2)cc1Cl
Reaction #191196
DOI: 10.1039/C8SC04228D
CC(C)CCC1(c2ccccc2)CC(O)=C(Sc2ccccc2)C(=O)O1
Reaction #201096
DOI: 10.1039/C8SC04228D
Страница 1Далее