部分構造検索

1156446

O=C1N(Cc2ncccc2C(F)(F)F)c2ccccc2C12COc1cc3c(cc12)OCCC3
Reaction #183490
DOI: 10.1039/C8SC04228D
O=C1N(Cc2ncccc2C(F)(F)F)c2ccccc2C12COc1cc3c(cc12)OCCO3
Reaction #489509
1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-2′(1′H)-one
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1(c2ncc(Br)cc2Cl)CC1)c1ncccc1C(F)(F)F
Reaction #666047
N-[[1-(5-bromo-3-chloro-2-pyridyl)cyclopropyl]methyl]-3-(trifluoromethyl)pyridine-2-carboxamide
収率 96.3%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc2c(cnn2Cc2ncccc2C(F)(F)F)c1
Reaction #1209178
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)C1(COc3cc4c(cc31)OCCO4)C(=O)N2Cc1ncccc1C(F)(F)F
Reaction #1296998
DOI: 10.1039/C8SC04228D
O=C1N(Cc2ncccc2C(F)(F)F)c2ccccc2C12COc1cc3c(cc12)OCCO3
Reaction #1298218
DOI: 10.1039/C8SC04228D
N#Cc1cc2c(cc1F)OCC21C(=O)N(Cc2ncccc2C(F)(F)F)c2ccccc21
Reaction #1300031
DOI: 10.1039/C8SC04228D
O=C1N(Cc2ncccc2C(F)(F)F)c2c(F)cccc2C12COc1cc3c(cc12)OCCO3
Reaction #1303002
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)C1(COc3cc4c(cc31)OCCO4)C(=O)N2Cc1ncccc1C(F)(F)F
Reaction #1494882
5′-methyl-1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-2′(1′H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2ncccc2C(F)(F)F)c2cccc(F)c2C12COc1cc3c(cc12)OCCO3
Reaction #1494907
4′-fluoro-1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-2′(1′H)-one
収率 82.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2ncccc2C(F)(F)F)c2ccccc2C12COc1cc3c(cc12)OCCC3
Reaction #1494909
1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-7,8-dihydro-6H-spiro[furo[2,3-g]chromene-3,3′-indol]-2′(1′H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2ncccc2C(F)(F)F)c2ccccc2C12COc1cc3c(cc12)OCOC3
Reaction #1494924
1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-2,3-dihydrospiro[furo[2,3-g][1,3]benzodioxine-8,3′-indol]-2′(1′H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2ncccc2C(F)(F)F)c2ccccc2[C@@]12COc1cc3c(cc12)OCOC3
Reaction #1494926
(8R)-1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-2,3-dihydrospiro[furo[2,3-g][1,3]benzodioxine-8,3′-indol]-2′(1′H)-one
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(cc1F)OCC21C(=O)N(Cc2ncccc2C(F)(F)F)c2ccccc21
Reaction #1494976
6-fluoro-2′-oxo-1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-1′,2′-dihydrospiro[1-benzofuran-3,3′-indole]-5-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2ncccc2C(F)(F)F)c2ccccc2C12COc1cc3c(cc12)OCCO3
Reaction #1862566
1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-2′(1′H)-one
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc2c(cnn2Cc2ncccc2C(F)(F)F)c1
Reaction #2036787
1-(3-Trifluoromethyl-pyridin-2-ylmethyl)-1H-indazole-5-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C1(COc3cc4c(cc31)OCCO4)C(=O)N2Cc1ncccc1C(F)(F)F
Reaction #2052740
5′-methyl-1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-2′(1′H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2ncccc2C(F)(F)F)c2cccc(F)c2C12COc1cc3c(cc12)OCCO3
Reaction #2052766
4′-fluoro-1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-2′(1′H)-one
収率 82.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2ncccc2C(F)(F)F)c2ccccc2C12COc1cc3c(cc12)OCCC3
Reaction #2052770
1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-7,8-dihydro-6H-spiro[furo[2,3-g]chromene-3,3′-indol]-2′(1′H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2ncccc2C(F)(F)F)c2ccccc2C12COc1cc3c(cc12)OCOC3
Reaction #2052786
1′-{[3-(trifluoromethyl)pyridin-2-yl]methyl}-2,3-dihydrospiro[furo[2,3-g][1,3]benzodioxine-8,3′-indol]-2′(1′H)-one
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ