Substructure Search

13995

O=C(NC1CC1)c1ccc(F)c(O)c1
Reaction #6966
3-hydroxy-4-fluoro-N-cyclopropylbenzamide
Yield 61.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(F)c(F)c(OC)c1F
Reaction #10369
title compound
Yield 98.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(OC)c(F)c(F)c1F
Reaction #10371
title compound
Yield 96.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(F)c(N2CCC(NC(=O)OC(C)(C)C)C2)c(OC)c1F
Reaction #10380
title compound
Yield 77.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1COc2c(F)c(F)cc3c(=O)[nH]c(=O)n1c23
Reaction #10418
title compound
Yield 15.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1COc2c(F)c(F)cc(C(=O)O)c2N1
Reaction #10436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCOc1cc(CO)ccc1F
Reaction #43339
title compound
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(F)cc(C)c(C(=O)O)c1N
Reaction #45566
2-Amino-4-fluoro-3-methoxy-6-methylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C(=O)O)c(C)c(I)c1F
Reaction #45567
compound
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(F)c(I)c(C)c2c(=O)oc(=O)[nH]c12
Reaction #45568
7-Fluoro-6-iodo-8-methoxy-5-methyl-1H-benzo[d][1,3]oxazine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(F)c(I)c(C)c(C(N)=O)c1NC(=O)C(C)C
Reaction #45585
compound
Yield 29.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #65947
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(CC)CC)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #65954
(R)-8-fluoro-5-methyloxycarbonyl-3-(N-3-pentyl-N-n-propylamino)chroman
DOI: 10.6084/m9.figshare.5104873.v1
N
Reaction #65955
NH3
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(C)C)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #65956
title compound
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccc(F)c(OCC2CC2)c1
Reaction #69062
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(c1ccc(F)cc1)c1ccc(F)c(OCC2CC2)c1
Reaction #69066
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)c1ccc(F)c(OCC2CC2)c1
Reaction #69067
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(C)C)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #80543
title compound
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN([C@H]1COc2c(F)ccc(C(=O)OC)c2C1)C(C)(C)C
Reaction #80547
Methyl (R)-3-(N-tert-Butyl-N-n-propylamino)-8-fluoro-3,4-dihydro-2H-1-benzopyran-5-carboxylate
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
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