Substructure Search

OCCCc1cccc(F)n1

OCCCc1cccc(F)n1
Reaction #81495
2-fluoro-6-(3-hydroxypropyl)pyridine
Yield 30.9%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CO1)c1cc(-c3cccnc3F)ccc1Oc1c2cc(C2=CCOCC2)nc1F
Reaction #423104
(S)-3-(3,6-dihydro-2H-pyran-4-yl)-1-fluoro-7-(2-fluoropyridin-3-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine
DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CO1)c1cc(-c3cccnc3F)ccc1Oc1c2cc(C2CCOCC2)nc1F
Reaction #423105
(S)-1-fluoro-7-(2-fluoropyridin-3-yl)-3-(tetrahydro-2H-pyran-4-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(C2CCOCC2)nc1F
Reaction #423135
2-fluoro-6-(tetrahydro-2H-pyran-4-yl)pyridin-3-ol
Yield 50.9%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1c(Br)cc(C2CCOCC2)nc1F
Reaction #423136
4-bromo-2-fluoro-3-(methoxymethoxy)-6-(tetrahydro-2H-pyran-4-yl)pyridine
Yield 58.4%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1ccc(C2CCOCC2)nc1F
Reaction #423137
2-fluoro-3-(methoxymethoxy)-6-(tetrahydro-2H-pyran-4-yl)pyridine
Yield 12.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cc(Br)ccc2oc2c(F)nc(C3CCOCC3)cc12
Reaction #423138
7-bromo-1-fluoro-3-(tetrahydro-2H-pyran-4-yl)-5H-chromeno[2,3-c]pyridin-5-one
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CS1)c1cc(-c3cccnc3F)ccc1Oc1c2cc(C2=CCOCC2)nc1F
Reaction #423198
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CS1)c1cc(-c3cccnc3F)ccc1Oc1c2cc(C2CCOCC2)nc1F
Reaction #423208
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2cc3c(c(F)n2)Oc2ccc(-c4cccnc4F)cc2[C@@]32CSC(N)=N2)CCO1
Reaction #423209
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)c1cccc(F)n1
Reaction #1036581
DOI: 10.1039/C8SC04228D
OCCCc1cccc(F)n1
Reaction #1050504
2-fluoro-6-(3-hydroxypropyl)pyridine
Yield 30.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(CN(C(=O)C2CC2c2cccc(F)n2)c2ccc(Br)cc2)CCCC1
Reaction #1234683
DOI: 10.1039/C8SC04228D
O=C(O)C(Cc1cccc(OC(F)(F)C(F)F)c1)C(O)c1cccc(F)n1
Reaction #1235496
DOI: 10.1039/C8SC04228D
CCC(C)C(CN(C(=O)C1CC1c1cccc(F)n1)c1ccc(Br)cc1)NC(=O)OC(C)(C)C
Reaction #1313961
DOI: 10.1039/C8SC04228D
CCOC(=O)CC(=O)c1cccc(F)n1
Reaction #1697686
ethyl 3-(6-fluoro-2-pyridyl)-3-oxopropionate
Yield 163.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1cccc(OC(F)(F)C(F)F)c1)C(=O)c1cccc(F)n1
Reaction #1697688
ethyl 3-(6-fluoropyridin-2-yl)-3-oxo-2-((3-(1,1,2,2-tetrafluoroethoxy)phenyl)methyl)propionate
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1cccc(OC(F)(F)C(F)F)c1)C(O)c1cccc(F)n1
Reaction #1697689
ethyl 3-(6-fluoropyridin-2-yl)-3-hydroxy-2-((3-(1,1,2,2-tetrafluoroethoxy)phenyl)methyl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Cc1cccc(OC(F)(F)C(F)F)c1)C(O)c1cccc(F)n1
Reaction #1697690
(2RS,3RS)-3-(6-fluoropyridin-2-yl)-3-hydroxy-2-((3-(1,1,2,2-tetrafluoroethoxy)phenyl)methyl)propionic acid
Yield 74.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(Cc2cccc(OC(F)(F)C(F)F)c2)C(c2cccc(F)n2)O1
Reaction #1697691
(4RS,5RS)-5-(6-fluoropyridin-2-yl)-4-((3-(1,1,2,2-tetrafluoroethoxy)phenyl)methyl)-1,3-oxazolidin-2-one
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
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