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565806

CC(N)(c1ccccc1)C1CCC2(CC1)OCCO2
Reaction #73479
pale yellow oil
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)(c1ccccc1)C1CCC(=O)CC1
Reaction #73480
4-(1-Amino-1-phenyl-ethyl)-cyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(C)(c1ccccc1)C1CCC(O)CC1
Reaction #73481
white foam
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)(c1ccccc1)C1CCC(O)CC1
Reaction #73482
4-(1-Amino-1-phenyl-ethyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)(c1ccccc1)C1CCC(Oc2cc3ccnc(OCc4ccccc4)c3cc2Cl)CC1
Reaction #73483
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)(N)C2CCC(Oc3cc4cc[nH]c(=O)c4cc3Cl)CC2)cc1
Reaction #73484
desired product
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(N)(c1ccc(F)cc1)C1CC(Oc2cc3ccnc(OC)c3cc2Cl)C1
Reaction #73487
1-[3-(7-chloro-1-methoxyisoquinolin-6-yloxy)-cyclobutyl]-1-(4-fluorophenyl)-propylamine
DOI: 10.6084/m9.figshare.5104873.v1
C=C(OCC)C1(NS(=O)C(C)(C)C)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560191
desired product 5
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NS(=O)C(C)(C)C)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560192
amino ester
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560193
ethyl 1′-amino-6′-bromo-4-methoxy-1′,3′-dihydrospiro[cyclohexane-1,2′-indene]-1′-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(OCC)C1(NS(=O)(=O)CC[Si](C)(C)C)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560195
N-(6′-bromo-1′-(1-ethoxyvinyl)-4-methoxy-1′,3′-dihydrospiro[cyclohexane-1,2′-indene]-1′-yl)-2-(trimethylsilyl)ethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NS(=O)(=O)CC[Si](C)(C)C)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560196
ethyl 6′-bromo-4-methoxy-1′-(2-(trimethylsilyl)ethylsulfonamido)-1′,3′-dihydrospiro[cyclohexane-1,2′-indene]-1′-carboxylate
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(N)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560197
methyl 1′-amino-6′-bromo-4-methoxy-1′,3′-dihydrospiro[cyclohexane-1,2′-indene]-1′-carboxylate
Выход 123.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NS(=O)C(C)(C)C)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560198
compound 6
Выход 56.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NS(=O)C(C)(C)C)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560203
compound 6
Выход 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560204
product 7
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NS(=O)C(C)(C)C)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560205
compound 6
Выход 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560206
compound 7
Выход 57.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560207
compound 7
Выход 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NS(=O)C(C)(C)C)c2cc(Br)ccc2CC12CCC(OC)CC2
Reaction #560208
compound 6
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
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