類似構造検索

87

N#Cc1ccc(N2CCCCC2)cc1F
Reaction #206
収率 49.4%
COc1cc(N2CCN(C(C)=O)CC2)ccc1Nc1ncc(Cl)c(-c2cnc3cc(N4CCCC4)ccn23)n1
Reaction #210
収率 0.0%
COc1cc(N2CCN(C(C)=O)CC2)ccc1Nc1ncc(Cl)c(-c2cnc3cc(N4CCCC4)ccn23)n1
Reaction #211
収率 2.0%
CCOC(=O)c1ccc(N2CCCCC2)cc1
Reaction #490
収率 81.4%
CC(C)(C)OC(=O)c1ccc(N2CCCCC2)nc1
Reaction #491
収率 61.9%
N#Cc1ccc(N2CCC2)cc1
Reaction #527
収率 62.0%
O=C(O)c1ccc(N2CCCCC2)c(Cl)c1
Reaction #647
収率 10.0%
c1cc2cn[nH]c2cc1N1CCCC1
Reaction #648
収率 93.7%
COc1ccc(N2CCN(C)CC2)c2c1CCN(C(=O)Cc1ccc(N3CCCCC3)cc1)C2
Reaction #708
収率 0.0%
O=Cc1cc(F)ccc1N1CCCC1
Reaction #767
収率 0.0%
Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CC3OC(=O)NC3=O)oc2c1
Reaction #1146
5-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranylmethyl]-2,4-oxazolidinedione
収率 6.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC=Cc1ccccc1Br)(C(=O)O)C(=O)O
Reaction #1357
desired product
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #1612
product
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #1681
product
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CCC(C(C)(C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1977
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #2186
product
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #2227
product
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #2285
product
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C=O)=Cc1ccccc1
Reaction #2499
α-hexylcinnamaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C=Cc1cccc(Br)c1
Reaction #2874
title compound
収率 94.4%DOI: 10.6084/m9.figshare.5104873.v1
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