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628538

CN(C)CCOC(=O)c1cc2cccc(O)c2[nH]1
Reaction #188265
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cccc(O)c2[nH]1
Reaction #225111
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(Cl)ccc(O)c2n1C
Reaction #233090
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(C(F)(F)F)ccc(OCc3ccccc3)c2n1C
Reaction #282831
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(C)ccc(O)c2[nH]1
Reaction #395631
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(C)ccc(O)c2[nH]1
Reaction #442875
ethyl 7-hydroxy-4-methyl-1H- indole-2-carboxylate
Ausbeute 6.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(Cl)ccc(OCc3ccccc3)c2n1C
Reaction #652179
Ethyl 7-benzyloxy-4-chloro-1-methyl-2-indolecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(Cl)ccc(O)c2n1C
Reaction #652180
Ethyl 4-chloro-7-hydroxy-1-methyl-2-indolecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C(F)(F)F)ccc(OCc3ccccc3)c2[nH]1
Reaction #652185
Ethyl 7-benzyloxy-4-trifluoromethyl-2-indolecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C(F)(F)F)ccc(OCc3ccccc3)c2n1C
Reaction #652186
Ethyl 7-benzyloxy-1-methyl-4-trifluoromethyl-2-indolecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C(F)(F)F)ccc(O)c2n1C
Reaction #652187
Ethyl 7-hydroxy-1-methyl-4-trifluoromethyl-2-indolecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(Cl)ccc(OCc3ccc(CNC(=O)OC(C)(C)C)cc3)c2n1C
Reaction #652238
ethyl 7-[4-(tert-butoxycarbonylaminomethyl)benzyloxy]-4-chloro-1-methyl-2-indolecarboxylate
Ausbeute 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CNC(N)=NC(=O)c1cc2c(Cl)ccc(OCc3ccc(CN)cc3)c2[nH]1.Cl.Cl
Reaction #652239
7-[4-(aminomethyl)benzyloxy]-4-chloro-1-methyl-2-indoloylguanidine dihydrochloride
Ausbeute 85.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(Cl)ccc(OCc3ccc(CN)cc3)c2n1C
Reaction #652240
ethyl 7-[4-(aminomethyl)benzyloxy]-4-chloro-1-methyl-2-indolecarboxylate
Ausbeute 101.2%DOI: 10.6084/m9.figshare.5104873.v1
CNC(N)=NC(=O)c1cc2c(Cl)ccc(OCc3ccc(CN(C)C)cc3)c2[nH]1.Cl.Cl
Reaction #652241
4-chloro-7-[4-(dimethylaminomethyl)benzyloxy]-1-methyl-2-indoloylguanidine dihydrochloride
Ausbeute 58.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C)ccc(O)c2[nH]1
Reaction #737236
ethyl 7-hydroxy-4-methyl-1H-indole-2-carboxylate
Ausbeute 6.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C(F)(F)F)ccc(O)c2n1C
Reaction #779838
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(C=O)ccc(OCc3ccccc3)c2[nH]1
Reaction #785449
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(C(=O)CN(Cc3ccccc3)C(C)CC(=O)OC)ccc(OCc3ccccc3)c2[nH]1
Reaction #901999
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(Cl)ccc(OCc3ccccc3)c2n1C
Reaction #923909
DOI: 10.1039/C8SC04228D
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