子结构搜索

CC(C)(C)CCO

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Reaction #52395
solid
收率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52396
solid
收率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCN3C2CC2)cc1
Reaction #52409
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CCN3C2CC2)cc1
Reaction #52411
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CCN3C2CC2)cc1F
Reaction #52412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(Sc2ccccc2)C1C(=O)OCc1ccc(F)c(Oc2ccccc2)c1
Reaction #56378
4-fluoro-3-phenoxybenzyl 3-phenylthio-2,2-dimethylcyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)CCOCC1
Reaction #57901
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccccn3)cc2)CCOCC1
Reaction #57903
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C(=O)c2cc(Cl)ccc2NS(=O)(=O)c2ccc(C3(C)CCOCC3)cc2)n1
Reaction #57904
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)CNC(=O)c1cccc(F)c1F)B1O[C@H]2C[C@H]3C[C@H](C3(C)C)[C@@]2(C)O1
Reaction #70023
2,3-difluoro-N-[2-({(1R)-3-methyl-1-[(3aR,4R,6R,7aS)-3a,5,5-trimethylhexahydro-4,6-methano-1,3,2-benzodioxaborol-2-yl]butyl}amino)-2-oxoethyl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)CNC(=O)c1cccc(F)c1F)B(O)O
Reaction #70024
[(1R)-1-({[(2,3-difluorobenzoyl)amino]acetyl}amino)-3-methylbutyl]boronic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)CNC(=O)c1ccccc1Br)B1O[C@@H]2C[C@@H]3C[C@@H](C3(C)C)[C@]2(C)O1
Reaction #70026
2-bromo-N-[2-({(1R)-3-methyl-1-[(3aS,4S,6S,7aR)-3a,5,5-trimethylhexahydro-4,6-methano-1,3,2-benzodioxaborol-2-yl]butyl}amino)-2-oxoethyl]benzamide
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79964
solid
收率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79965
solid
收率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCN3C2CC2)cc1
Reaction #79978
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CCN3C2CC2)cc1
Reaction #79980
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CCN3C2CC2)cc1F
Reaction #79981
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nnc(NCC2(c3ccc(OCCCN4CCCC4)cc3)CCOCC2)c2ccccc12
Reaction #187392
DOI: 10.1039/C8SC04228D
COC(=O)C1(CS(=O)(=O)c2ccc(Oc3ccc(Cl)cc3)cc2)CCOCC1Cc1ccccc1
Reaction #189091
DOI: 10.1039/C8SC04228D
CC(c1ccc(-c2ncc(C(=O)NC3CC3)s2)cc1)N1CCC(CC(C)(C)C#N)(c2ccccc2)OC1=O
Reaction #193631
DOI: 10.1039/C8SC04228D
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