Busqueda de Subestructura

12052

O=C(O)c1c(OCc2ccccc2)cc(F)c(F)c1F
Reaction #5665
6-benzyloxy-2,3,4-trifluorobenzoic acid
Rendimiento 31.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(F)cc(F)c(F)c1F
Reaction #10365
title compound
Rendimiento 60.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1c(F)c(F)c(F)c(F)c1F
Reaction #10367
title compound
Rendimiento 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(F)cc(N2CC[C@H](NC(=O)OC(C)(C)C)C2)c(F)c1F
Reaction #10376
title compound
Rendimiento 69.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(c2c(F)c(F)c(C(=O)OCc3ccccc3)c(F)c2F)C1
Reaction #10378
title compound
Rendimiento 63.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1c(F)c(F)c(F)c(F)c1F
Reaction #254209
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1c(F)cc(F)c(F)c1F
Reaction #256588
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(F)c(F)c(O)c(F)c1F
Reaction #357409
4-hydroxy-2,3,5,6-tetrafluorobenzoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(F)c(F)c(O)c(F)c1F
Reaction #789331
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(F)cc(F)c(F)c1F
Reaction #816540
title compound
Rendimiento 60.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1c(F)c(F)c(F)c(F)c1F
Reaction #816542
title compound
Rendimiento 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(F)cc(N2CC[C@H](NC(=O)OC(C)(C)C)C2)c(F)c1F
Reaction #816551
title compound
Rendimiento 69.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(c2c(F)c(F)c(C(=O)OCc3ccccc3)c(F)c2F)C1
Reaction #816553
title compound
Rendimiento 63.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC(=O)c1c(F)c(F)c(F)c(F)c1F
Reaction #1219595
DOI: 10.1039/C8SC04228D
CC(=O)OC(=O)c1c(F)c(F)c(F)c(F)c1F.CCCC[C@H](NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)c1ccccc1)C(C)C)C(=O)O
Reaction #1723511
N-Benzoyl-L-valyl-L-alanyl-L-norleucine 2,3,4,5,6-pentafluoro benzoyloxy methyl ketone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(OCc2ccccc2)cc(F)c(F)c1F
Reaction #1741670
6-benzyloxy-2,3,4-trifluorobenzoic acid
Rendimiento 31.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1c(F)cc(F)c(F)c1F
Reaction #2135261
title compound
Rendimiento 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(F)cc(N2CCC(NC(=O)OC(C)(C)C)C2)c(F)c1F
Reaction #2234770
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCN(c2c(F)c(F)c(C(=O)OCc3ccccc3)c(F)c2F)C1
Reaction #2236356
DOI: 10.1039/C8SC04228D