Substructure Search

9290

N#Cc1ccc(OCCCCCCl)cc1
Reaction #6164
4-(5-chloropentoxy) benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC(N2CCCCCC2=O)CC1
Reaction #48499
title compound
Yield 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1C(F)(Cl)CCCC1(Cl)Br
Reaction #50106
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
FC1(Cl)CCC2OC2(Br)C1
Reaction #50107
epoxide
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63588
intermediate 17
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63589
intermediate 18
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)N1CCCC2CCCCC21
Reaction #67495
4-bromo-1-(octahydroquinolin-1-yl)butan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
[O-]B[O-]
Reaction #81913
boronate
DOI: 10.6084/m9.figshare.5104873.v1
[O-]B[O-]
Reaction #82148
boronate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)N1CCCC2CCCCC21
Reaction #155512
4-bromo-1-(octahydroquinolin-1-yl)butan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCBr)NCc1ccccn1
Reaction #189149
DOI: 10.1039/C8SC04228D
BrCCCCCOCC1CCCCC1
Reaction #193863
DOI: 10.1039/C8SC04228D
O=C(Cl)C(CCCBr)(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #194732
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCc2cc(N3CCCCC3=O)ccc21
Reaction #196317
DOI: 10.1039/C8SC04228D
O=Cc1ccccc1OCCCCCCl
Reaction #211764
DOI: 10.1039/C8SC04228D
O=C(CO)CCCCBr
Reaction #213917
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CO)CCCCBr
Reaction #214273
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cccc1NC(=O)CCCCBr
Reaction #223956
DOI: 10.1039/C8SC04228D
COc1ccc(C(C#N)(CCCCCCl)SC2CCCCC2)cc1OC
Reaction #226786
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCCCCCl)C(C)=O
Reaction #227566
DOI: 10.1039/C8SC04228D
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