Recherche de Sous-structure

1327563

O=C(O)CCC#Cc1ccccc1
Reaction #6818
5-phenylpent-4-ynoic acid
Rendement 28.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCC#Cc1ccccc1
Reaction #6819
(4-phenyl-but-3-ynyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(CC(=O)C(C)CCCc1ccccc1)OC
Reaction #87967
title compound
Rendement 98.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(S(=O)(=O)C(C#Cc3ccccc3)C(N)(OC)C(=O)O)cc2)cc1
Reaction #180114
DOI: 10.1039/C8SC04228D
O=C(O)CCC#Cc1ccc(C(F)(F)F)cc1
Reaction #181171
DOI: 10.1039/C8SC04228D
O=C(CCc1ccco1)NCCC1(C2CCCC2)CC(=O)C(Cl)C(=O)O1
Reaction #184110
DOI: 10.1039/C8SC04228D
COC(=O)C(CC#Cc1ccc(Oc2ncccn2)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #185618
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(C)Oc1ccc(CNC(=O)CCC#Cc2ccc(OC(F)(F)F)cc2)cc1
Reaction #187366
DOI: 10.1039/C8SC04228D
N#Cc1ccc(C#CCCC(=O)O)cc1
Reaction #188675
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)C2(CCCc3ccc(Cl)cc3)SC(=O)NC2=O)cc1
Reaction #192698
DOI: 10.1039/C8SC04228D
COC(=O)CCC#Cc1ccc(OC(F)(F)F)cc1
Reaction #207724
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(CC#Cc2ccc(Cl)cc2)(Sc2ccc(F)cc2)S1
Reaction #213285
DOI: 10.1039/C8SC04228D
COC(=O)CCC#Cc1c(F)ccc2c1C(=Cc1[nH]ccc1OC)C(=O)N2
Reaction #225947
DOI: 10.1039/C8SC04228D
COc1ccc(C(C#Cc2ccccc2)CC(=O)CO)cc1OC1CCCC1
Reaction #228889
DOI: 10.1039/C8SC04228D
O=CCCC#Cc1ccccc1
Reaction #240316
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(CC#Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)(S(=O)(=O)c2ccccn2)S1
Reaction #246374
DOI: 10.1039/C8SC04228D
NC(CC#Cc1ccccc1)(C(=O)O)S(=O)(=O)c1ccc(-c2ccc3c(c2)OCO3)cc1
Reaction #251588
DOI: 10.1039/C8SC04228D
Cc1cccc(C#CC2(C3CCCC3)CC(=O)CC(=O)O2)c1
Reaction #252042
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(CC=Cc1ccc(Br)cc1)C(=O)OC1CCCC1
Reaction #256539
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(CC#Cc2ccc(Cl)cc2)(Sc2nc3cc(Cl)ccc3s2)S1
Reaction #265388
DOI: 10.1039/C8SC04228D
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