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742638

CCOP(=O)(Cc1cccc(N)c1)OCC
Reaction #180384
DOI: 10.1039/C8SC04228D
CCCCCCCCOc1ccc(-c2ccc(C(=O)N(C)c3cccc(C(F)(F)P(=O)(O)OCC)c3)cc2)cc1
Reaction #235024
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cccc(C=Cc2ccnc3ccccc23)c1
Reaction #258986
DOI: 10.1039/C8SC04228D
CCOP(=O)(OCC)C(OC)c1cc(OC)cc([N+](=O)[O-])c1
Reaction #444815
phosphonate
Выход 86.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=C1C2CC3CC(C2)CC1C3)c1cc(NC(=O)C(F)(F)F)cc(OC)c1
Reaction #444816
enol ether
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)C(OC)c1cc(OC)cc([N+](=O)[O-])c1
Reaction #457490
phosphonate
Выход 86.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=C1C2CC3CC(C2)CC1C3)c1cc(NC(=O)C(F)(F)F)cc(OC)c1
Reaction #457491
enol ether
DOI: 10.6084/m9.figshare.5104873.v1
COC(=C1C2CC3CC(C2)CC1C3)c1cc(NC(=O)C(F)(F)F)cc(OC)c1
Reaction #464132
enol ether
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(Cc1cc(-c2ccccc2Cl)c2c(c1)N(c1c(Cl)cccc1Cl)C(=O)NC2)OCC
Reaction #481295
diethyl [5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2-oxo-1,2,3,4-tetrahydroquinazolin-7-yl]methylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=Cc2cc(-c3ccccc3Cl)c3c(c2)N(c2c(Cl)cccc2Cl)C(=O)NC3)CC1
Reaction #481296
tert-butyl 4-{[5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2-oxo-1,2,3,4-tetrahydroquinazolin-7-yl]methylene}piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(Cc1cccc([N+](=O)[O-])c1)OCC
Reaction #598391
diethyl (3-nitrobenzyl)phosphonate
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(Cc1cccc(N)c1)OCC
Reaction #598392
diethyl (3-aminobenzyl)phosphonate
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OP(=O)(Cc1cccc([N+](=O)[O-])c1)OC(C)C
Reaction #598436
dipropan-2-yl (3-nitrobenzyl)phosphonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OP(=O)(Cc1cccc(Nc2ncc(C(F)(F)F)c(NCc3cccnc3N(C)S(C)(=O)=O)n2)c1)OC(C)C.O=C(O)C(F)(F)F
Reaction #598437
dipropan-2-yl [3-({4-[({2-[methyl (methylsulfonyl)amino]pyridin-3-yl}methyl)amino]-5-(trifluoromethyl)pyrimidin-2-yl}amino)benzyl]phosphonate trifluoroacetate
Выход 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(Cc1cccc([N+](=O)[O-])c1)OCC
Reaction #602544
title compound
Выход 63.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=Cc2cccc([N+](=O)[O-])c2)CC1
Reaction #602545
tert-butyl 4-(3-nitrobenzylidene)-piperidine-1-carboxylate
Выход 85.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OP(=O)(Cc1cccc([N+](=O)[O-])c1)OC(C)C
Reaction #754069
DOI: 10.1039/C8SC04228D
CCOP(=O)(Cc1cc(-c2ccccc2Cl)c2c(c1)N(c1c(Cl)cccc1Cl)C(=O)NC2)OCC
Reaction #756224
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(=Cc2cc(-c3ccccc3Cl)c3c(c2)N(c2c(Cl)cccc2Cl)C(=O)NC3)CC1
Reaction #888462
DOI: 10.1039/C8SC04228D
CCOP(=O)(Cc1cccc(N)c1)OCC
Reaction #1051819
diethyl 3-aminobenzylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
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