Busqueda de Subestructura

OB(O)c1cccc(F)c1

CCCCCOCCCCOc1ccc(B(O)O)c(F)c1F
Reaction #6687
2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOCCCCOc1ccc(-c2ccc(C(=O)OCC)cc2)c(F)c1F
Reaction #6688
2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid ethyl ester
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOCCCCOc1ccc(B(O)O)c(F)c1F
Reaction #6693
2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOCCCCOc1ccc(-c2ccc(C(=O)OCC)cc2)c(F)c1F
Reaction #6694
2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid ethyl ester
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C2(Br)C=CC=CC2)c(F)c1F
Reaction #7430
formula 13
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)cc1F
Reaction #9429
desired product
Rendimiento 69.0%DOI: 10.6084/m9.figshare.5104873.v1
OB(O)c1cc(F)ccc1OC1CCCCO1
Reaction #41917
5-Fluoro-2-(tetrahydropyran-2-yloxy)benzeneboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](C[N+](=O)[O-])c1cccc(F)c1F)C(=O)OCc1ccccc1
Reaction #42668
title compound
Rendimiento 87.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cccc(F)c2)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45726
compound
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cc(F)cc(F)c2)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45729
2-Cyclopropyl-6-(3,5-difluorophenyl)-7-fluoro-5-methyl-1,3-benzoxazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cccc(F)c2F)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45731
compound
Rendimiento 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cccc(F)c2)c(F)c2oc(C(=O)N(C)C)nc2c1C#N
Reaction #45744
compound
Rendimiento 36.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cc(F)cc(F)c2)CC1
Reaction #48125
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cccc(F)c2)CC1
Reaction #48132
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H](NC(=O)OCc1ccccc1)C(=O)N(CC(=C)c1cccc(F)c1F)Cc1ccc(OC)cc1OC
Reaction #48407
title compound
Rendimiento 69.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](C[N+](=O)[O-])c1cccc(F)c1F)C(=O)OCc1ccccc1
Reaction #48412
title compound
Rendimiento 87.4%DOI: 10.6084/m9.figshare.5104873.v1
COCCn1cc(-c2cccc(F)c2F)cc([N+](=O)[O-])c1=O
Reaction #48453
title compound
Rendimiento 59.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2cc(F)cc(F)c2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48786
title compound
Rendimiento 22.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Oc2cc(O[C@@H](C)CO)cc(C(=O)Nc3ccn(C)n3)c2)cc1F
Reaction #48807
desired compound
Rendimiento 30.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCSCC1=CC(C)(C)Nc2ccc(-c3cc(F)ccc3OC)cc21
Reaction #54089
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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