子结构搜索

4732

COc1cc(C)cc(Sc2cccc(F)c2C#N)c1
Reaction #941
2-Fluoro-6-[(3 -methyl-5-methoxyphenyl)thio]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #3457
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-butanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #3466
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-pentanone
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)C1CC1
Reaction #3470
N-methoxy-N-methylcyclopropylcarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)Cc1cc(OC)ccc1NC(=O)OC(C)(C)C
Reaction #3477
1-(2-(tert-butoxycarbonylamino)-5-methoxyphenyl]-2-butanone
收率 74.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(Cc2ccccc2)CC1Cc1ccc2ccccc2c1
Reaction #10273
4-benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCO[Si](OCC)(OCC)C(F)=C(F)F
Reaction #12072
CF2═CFSi(OEt)3
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #12074
(C6F5)2Si(OEt)2
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)c1nccc2ccc(C(=O)O)cc12
Reaction #42541
1-[butyl(methyl)amino]isoquinoline-7-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nccc2ccc(C(=O)O)cc12
Reaction #42544
1-butylisoquinoline-7-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
C#C[C@@H]1CCCN1C(=O)OC(C)(C)C
Reaction #45451
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(=O)n(C)c(C3CCCN(C(=O)OCc4ccccc4)C3)c(-c3ccccc3)c2c1
Reaction #46144
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(c1ccccc1)C(O)(C1CCN(C(=O)OCc3ccccc3)CC1)N(C)C2=O
Reaction #46149
benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate
收率 49.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc(Cl)cc1C(O)c1ccc(Br)cc1
Reaction #47968
tert-butyl {2-[(4-bromophenyl)(hydroxy)methyl]-4-chlorophenyl}carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccccc1)N1C(=O)c2cccc(Cl)c2C1O
Reaction #49284
4-chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccccc1)N1C(=O)c2c(I)ccc(Cl)c2C1O
Reaction #49285
4-chloro-3-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccccc1)N1C(=O)c2cccc(F)c2C1O
Reaction #49349
4-fluoro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
收率 93.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccccc1)N1C(=O)c2c(I)ccc(F)c2C1O
Reaction #49350
4-fluoro-3-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
收率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49353
4-methoxy-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(I)c2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49354
4-methoxy-3-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
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