部分構造検索

OC1CCOc2ccccc21

COC(=O)c1ccc(OC(=O)C2CCOc3ccccc32)cc1OC
Reaction #1778
methyl 4-(4-chromanoyloxy)-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c1OCCC2O
Reaction #3865
desired product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3866
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCOC1=CCOc2ccccc21
Reaction #47110
product 475
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)CCCO2
Reaction #51201
title product
収率 85.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2ccc3c(c2)C(O)CC(c2ccccc2C(F)(F)F)O3)nc1
Reaction #59582
6-(5-Nitropyridin-2-yloxy)-2-(2-trifluoromethylphenyl)chroman-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC1CCOc2ccccc21
Reaction #60342
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C(F)(F)C(F)(F)F)cc2C2OC21
Reaction #65152
3,4-dihydro-2,2-dimethyl-3,4-epoxy-6-pentafluoroethyl-2H-1-benzopyran
収率 96.2%DOI: 10.6084/m9.figshare.5104873.v1
NCC1(O)CCOc2cc(Br)ccc21
Reaction #91895
4-(aminomethyl)-7-bromo-3,4-dihydro-2H-1-benzopyran-4-ol
収率 79.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2[C@@H](N)[C@@H]1O
Reaction #93185
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2[C@@H](N2CCCC2=O)[C@@H]1O
Reaction #93186
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2[C@@H](N2CCCCC2=O)[C@@H]1O
Reaction #93187
6-cyano-3,4-dihydro-2,2-dimethyl-trans-4-(2-oxo-1-piperidinyl)-2H-benzo[b]pyran-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c1OCCC2O
Reaction #93285
desired product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93286
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2C(NNC(N)=O)C1O
Reaction #173415
DOI: 10.1039/C8SC04228D
COC1=CC(=O)N(C2c3cc(C#N)ccc3OC(C)(C)C2O)C1
Reaction #173610
DOI: 10.1039/C8SC04228D
Cc1cccc(COc2ccc3c(c2)C(O)C(Cc2ccccc2)CO3)n1
Reaction #179529
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(CC2COc3ccc(OCc4nc5cc(F)ccc5s4)cc3C2O)c1
Reaction #181772
DOI: 10.1039/C8SC04228D
CC(C)c1cc2c(c(C3=CCCCC3)c1C(=O)c1ccc(C(F)(F)F)cc1)C(O)CC(C)(C)O2
Reaction #186129
DOI: 10.1039/C8SC04228D
CC1(C)Oc2ccc(C#N)cc2C(OC(=O)C2CCCN2S(=O)(=O)c2ccc([N+](=O)[O-])cc2)C1Br
Reaction #194838
DOI: 10.1039/C8SC04228D
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