2,3-dihydrofuran

CC(=O)c1ccc2c(c1)CCO2
Reaction #3100
title compound
収率 186.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(NCC(F)(F)CN1CCOCC1)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6981
title compound
収率 51.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1cccc(C2CC=CO2)c1
Reaction #10843
3-(2,3-dihydro-furan-2-yl)-benzaldehyde
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(OC)c(C2C=CCO2)cc1C=O
Reaction #10845
5-(2,5-dihydro-furan-2-yl)-2,4-dimethoxy-benzaldehyde
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC3CCCO3)cc2n1Cc1ccccc1
Reaction #68332
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)C1Nc2c(Cl)cc(Cl)c(Cl)c2C2OCCC12
Reaction #75693
Compound 67
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(=O)N1C=C(c2ccccc2)N(CC(=O)N[C@@H](Cc2ccccc2)C(=O)C2=CCCO2)C(=O)C1C(C)C
Reaction #78914
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(=O)c1ccc2c(c1)CCO2
Reaction #82853
title compound
収率 186.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #193438
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCCC=P(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #197603
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214867
1-(2-tetrahydrofuryl)-5-fluorouracil
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214868
1-(2-tetrahydrofuryl)-5-fluorouracil
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214869
1-(2-tetrahydrofuryl)-5-fluorouracil
収率 71.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214870
1-(2-tetrahydrofuryl)-5-fluorouracil
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214871
1-(2-tetrahydrofuryl)-5-fluorouracil
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214872
1-(2-tetrahydrofuryl)-5-fluorouracil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214873
1-(2-tetrahydrofuryl)-5-fluorouracil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214874
1-(2-tetrahydrofuryl)-5-fluorouracil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214875
1-(2-tetrahydrofuryl)-5-fluorouracil
収率 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=c1[nH]c(=O)n(C2CCCO2)cc1F
Reaction #214876
1-(2-tetrahydrofuryl)-5-fluorouracil
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
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