子结构搜索

1065768

COCCOCOc1c(C#N)ccc(C(Br)C(=O)OC(c2ccccc2)c2ccccc2)c1OCOCCOC
Reaction #2673
Diphenylmethyl [4-cyano-2,3-bis-[(2-methoxy-ethoxy]-methoxy]phenyl]-bromoacetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1cccc(OC)c1
Reaction #94574
methyl bromo-(m-methoxyphenyl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1cc2c(cc1Cl)OCO2
Reaction #192298
DOI: 10.1039/C8SC04228D
COC(=O)C(Br)c1cccc(OC)c1
Reaction #230465
DOI: 10.1039/C8SC04228D
COC(=O)C(Br)c1cccc(OC)c1
Reaction #265087
DOI: 10.1039/C8SC04228D
COC(=O)C(Br)c1cccc(OC)c1
Reaction #272371
DOI: 10.1039/C8SC04228D
COC(=O)C(Br)c1cccc(OC)c1
Reaction #311481
methyl bromo-(m-methoxyphenyl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1cccc(OC)c1
Reaction #358102
Bromo-(3-methoxy-phenyl)-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(c1cccc(OC)c1)n1nc(C(F)(F)F)c(Cl)c1C
Reaction #358103
(4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-(3-methoxy-phenyl)-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1ccc2c(c1)OCO2
Reaction #362109
methyl 2-bromo-2-(3,4-methylenedioxyphenyl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(CO)cc(Cl)c1OC(C(=O)OC)c1ccc2c(c1)OCO2
Reaction #362114
title compound
收率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(Cn2c(=O)n(C(=O)OCC)c3ccccc32)ccc1OC(C(=O)OCC)c1ccc2c(c1)OCO2
Reaction #362123
title compound
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(Br)C(=O)OC(C)(C)C)cc1OC
Reaction #379681
DOI: 10.1039/C8SC04228D
COC(=O)C(c1ccc2c(c1)OCO2)c1cn(C)c2cc(CO)ccc12
Reaction #388262
DOI: 10.1039/C8SC04228D
COC(=O)C(Br)c1cccc(OC)c1
Reaction #389207
DOI: 10.1039/C8SC04228D
Cn1cc(C(C(=O)O)c2ccc3c(c2)OCO3)c2cc(Br)ccc21
Reaction #456522
subtitle compound
收率 79.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1ccc2c(c1)OCO2
Reaction #468503
Methyl 2-(1,3-benzodioxol-5-yl)-2-bromoacetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1ccc2c(c1)OCO2)c1cn(C)c2cc(CO)ccc12
Reaction #468504
subtitle compound
收率 77.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1ccc2c(c1)OCO2)c1cn(C)c2ccc(Br)cc12
Reaction #468508
subtitle compound
收率 76.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1cc(OC)c2c(c1)OCO2)c1c[nH]c2cc(Br)ccc12
Reaction #468511
subtitle compound
收率 88.9%DOI: 10.6084/m9.figshare.5104873.v1
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