類似構造検索

O=C(O)c1ccc(OC2CCCCO2)cc1

O=C(O)c1ccc(OC2CCCCO2)cc1
Reaction #7427
p-tetrahydropyranyloxy benzoic acid
収率 86.2%DOI: 10.6084/m9.figshare.5104873.v1
Ic1ccc(OC2CCCCO2)cc1
Reaction #10571
1
収率 92.1%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1ccc(OC2CCCCO2)cc1
Reaction #10572
4-Tetrahydropyranyloxy-1-(trimethylsilylethynyl) benzene
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(OC2CCCCO2)cc1
Reaction #10573
4-Tetrahydropyranyloxyphenylacetylene
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(C#Cc2ccc(OC3CCCCO3)cc2)cc1
Reaction #10574
4-Tetrahydropyranyloxy-4′-trifluormethyltolan
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(OCc2ccccc2)ccn1-c1ccc(OC2CCCCO2)cc1
Reaction #43312
title compound
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=Cc1cccc(Br)c1)c1ccc(OC2CCCCO2)cc1
Reaction #44817
powder
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=Cc1cccc(Cl)c1Cl)c1ccc(OC2CCCCO2)cc1
Reaction #44818
powder
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(OC2CCCCO2)cc1
Reaction #66533
sub-title compound
収率 133.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(OCCO)cc1
Reaction #205515
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C(c1ccc(OC2CCCCO2)cc1)c1cnco1
Reaction #207706
DOI: 10.1039/C8SC04228D
c1ccc(OC2CCCCO2)cc1
Reaction #216990
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)SC2CC(=O)N2C1C#N
Reaction #228680
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(OCCCCCCOC2CCCCO2)cc1
Reaction #230499
DOI: 10.1039/C8SC04228D
CNC(=O)c1nc(-c2ccc(OC3CCCCO3)cc2)cnc1N
Reaction #230882
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(-c2ccc(OC3CCCCO3)cc2)cc2nn(C3CCCCO3)cc12
Reaction #232487
DOI: 10.1039/C8SC04228D
C(=Nc1ccc(OCCN2CCCC2)cc1)c1ccc(OC2CCCCO2)cc1
Reaction #241648
DOI: 10.1039/C8SC04228D
O=C(ON1C(=O)CCC1=O)c1cc(OC2CCCCO2)cc(OC2CCCCO2)c1
Reaction #241889
DOI: 10.1039/C8SC04228D
FC(F)(F)Oc1ccc(N2CCN(c3ccc(OC4CCCCO4)cc3)CC2)cc1
Reaction #243681
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(OCCOC2CCCCO2)cc1
Reaction #254783
DOI: 10.1039/C8SC04228D
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