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281806

CCCCCC(C=Cc1ccc(C(=O)OC)cc1)c1ccc2c(c1)N(C)CCC2(C)C
Reaction #204420
DOI: 10.1039/C8SC04228D
CCCCCC(C=Cc1ccc(C(=O)O)cc1)c1ccc2c(c1)OCCC2(C)C
Reaction #259035
DOI: 10.1039/C8SC04228D
CCCCCC(C=Cc1ccc(C(=O)O)cc1)c1ccc2c(c1)N(C)CCC2(C)C
Reaction #274308
DOI: 10.1039/C8SC04228D
Cc1cc(C2=CC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)ON2C)ccc1C(=O)O
Reaction #294795
DOI: 10.1039/C8SC04228D
Cc1cc(C2=CC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)ON2C)ccc1C(=O)O
Reaction #300480
DOI: 10.1039/C8SC04228D
CCCCCC(CCc1ccc(C(=O)O)cc1)c1ccc2c(c1)C(C)(C)CCC2(C)C
Reaction #482107
titled compound
収率 69.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(/C=C/c1ccc(C(=O)OC)cc1)c1ccc2c(c1)C(C)(C)CCS2
Reaction #482118
ester
収率 39.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(/C=C/c1ccc(C(=O)O)cc1)c1ccc2c(c1)C(C)(C)CCS2
Reaction #482119
product
収率 95.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=CC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)ON2C)ccc1C(=O)O
Reaction #492877
4-[5-(3,5-Dichloro-phenyl)-2-methyl-5-trifluoromethyl-2,5-dihydro-isoxazol-3-yl]-2-methyl-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C2=CC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)ON2C)cc1C
Reaction #492878
4-[5-(3,5-Dichloro-phenyl)-2-methyl-5-trifluoromethyl-2,5-dihydro-isoxazol-3-yl]-2-methyl-benzoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=CC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)ON2C)ccc1C(=O)O
Reaction #492879
4-[5-(3,5-Dichloro-phenyl)-2-methyl-5-trifluoromethyl-2,5-dihydro-isoxazol-3-yl]-2-methyl-benzoic acid
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N1OC(C)(c2cc(Cl)cc(Cl)c2)C=C1c1ccc(C(=O)OC(C)(C)C)c(C)c1
Reaction #492881
3-(4-tert-butoxycarbonyl-3-methyl-phenyl)-5-(3,5-dichloro-phenyl)-5-methyl-5H-isoxazole-2-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=CC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)ON2C)ccc1CO
Reaction #492884
{4-[5-(3,5-Dichloro-phenyl)-2-methyl-5-trifluoromethyl-2,5-dihydro-isoxazol-3-yl]-2-methyl-phenyl}-methanol
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(/C=C/C(c2cc(Cl)cc(Cl)c2)C(F)(F)F)cc1C
Reaction #674379
title compound
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(/C=C/C(c2cc(Cl)cc(Cl)c2)C(F)(F)F)ccc1C(=O)O
Reaction #674380
title compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(/C=C/C(c2cc(Cl)cc(Cl)c2)C(F)(F)F)ccc1C(=O)NCC(F)(F)F
Reaction #674381
semi-solid
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(/C=C/C(c2cc(Cl)cc(Cl)c2)C(F)(F)F)ccc1C(=O)NCc1cncnc1
Reaction #674382
title compound
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=O)c1ccc(/C=C/C(c2cc(Cl)c(Cl)c(Cl)c2)C(F)(F)F)cc1Cl)NCC(F)(F)F
Reaction #674383
title compound
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=O)c1ccc(/C=C/C(c2cc(Cl)c(F)c(Cl)c2)C(F)(F)F)cc1Br)NCC(F)(F)F
Reaction #674384
title compound
収率 31.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(/C=C\C(c2cc(Cl)c(Cl)c(Cl)c2)C(F)(F)F)cc1Br
Reaction #674387
title compound
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
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