部分構造検索

CC(=O)OO

COc1cccc(S(=O)(=O)c2cccc(F)c2C#N)c1
Reaction #933
2-Fluoro-6-[(3 -methoxyphenyl)sulfonyl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(S(=O)c2cccc(F)c2C#N)c1
Reaction #935
2-Fluoro-6-[(3-methoxyphenyl)sulfinyl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(Br)[nH]c2c1C(=O)CCC2
Reaction #1005
2-bromo-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid
収率 29.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCOCC1(C)CO1
Reaction #1198
1,2-epoxy-2-methyl-3-tetradecyloxypropane
収率 79.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC(O)C1CO1
Reaction #1216
1,2-epoxy-3-tridecanol
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1310
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1316
Compound I
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3C(C)=S)cc1
Reaction #1338
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCCCCCCCCCCC.C=CN1CCCC1=O
Reaction #1498
lauryl methacrylate N-vinyl-2-pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CBr)cc1
Reaction #1517
4-bromomethylbenzoic acid
収率 65.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CCl)ccc[n+]1[O-]
Reaction #1777
3-Chloromethyl-2-methylpyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(CCl)ccc[n+]1[O-]
Reaction #1783
2-ethyl-3-chloromethylpyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(CCl)ccc[n+]1[O-]
Reaction #1786
2-isopropyl-3-chloromethylpyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc[n+]([O-])c(C)c1CCl
Reaction #1789
2,4-dimethyl-3-chloromethylpyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)c[n+]1[O-]
Reaction #1952
title compound
収率 22.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cc(-n2nc(CCC3CO3)[nH]c2=O)c(Cl)cc1Cl
Reaction #2058
title compound
収率 95.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc[n+]([O-])cc1
Reaction #2249
4-acetyl-pyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1ccc(-c2ccnc(Nc3cccc(Cl)c3)n2)cc1
Reaction #2254
N-(3-chloro-phenyl)-4-(N-oxido4-pyridyl)-2-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
C=CC12C=C(OCOCCOC)C(OCOCCOC)=C(Cl)C1(Cl)O2
Reaction #2676
expected product
収率 99.6%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N=C(c2ccccc2)c2ccccc2)c(CBr)c1
Reaction #2851
title compound
収率 56.9%DOI: 10.6084/m9.figshare.5104873.v1
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