#8632413

OC(COc1ccc(C(F)(F)F)cc1)COc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #175632
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(COCCOCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl)=NOC(C)(C)C
Reaction #182770
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(COCCCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl)OCC
Reaction #188337
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
ClC(Cl)=CCOc1cc(Cl)c(OCCCBr)c(Cl)c1
Reaction #193808
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
ClC(Cl)=CCOc1cc(Cl)c(OCc2ccc(Cl)nc2)c(Cl)c1
Reaction #194913
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #226967
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #241224
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #257863
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
ClC(Cl)=CCOc1cc(Cl)c(OCCCBr)c(Cl)c1
Reaction #263640
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #270480
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #272048
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
ClC(Cl)=CCOc1cc(Cl)c(OCCCOc2ccccc2)c(Cl)c1
Reaction #380014
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
ClC(Cl)=CCOCCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #383802
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Fc1cccc(C=CCCOc2c(Cl)cc(OCC=C(Cl)Cl)cc2Cl)c1
Reaction #390211
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Fc1ccc(C2(CCCOc3c(Cl)cc(OCC=C(Cl)Cl)cc3Cl)OCCO2)cc1
Reaction #404035
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
OCCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #405647
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
ClC(Cl)=CCOc1cc(Cl)c(OCCCBr)c(Cl)c1
Reaction #410853
3,5-dichloro-4-(3-bromopropoxy)-1-(3,3-dichloro-2-propenyloxy)benzene
수율 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=C1c2ccccc2C(=O)N1CCCCOc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #410858
3,5-dichloro-4-(4-phthalimidobutyloxy)-1-(3,3-dichloro-2-propenyloxy)benzene
수율 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOC(=O)C(CC)Oc1c(Cl)cc(OCC=C(Cl)Cl)cc1Cl
Reaction #410861
ethyl 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxybutyrate
수율 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
ClC(Cl)=CCOc1cc(Cl)c(OCCCCc2ccccc2)c(Cl)c1
Reaction #450239
3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-phenylbutyloxy)benzene
수율 73.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
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