Substructure Search

323661

CCCCCC(O)C=CCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #54873
4-(4-Acetyl-8-hydroxytridec-6-en-1-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(C)(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #54875
4-(4-Acetyl-8-hydroxy-8-methyltridecyl)benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[C@@H]1C/C=C/CCC(=O)O[C@H](c2ccccc2)CNC1=O)NCc1ccc(Cl)nc1
Reaction #69351
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[C@@H]1C/C=C/CCC(=O)N[C@H](c2ccccc2)COC1=O)NCc1ccc(Cl)cc1
Reaction #69355
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCC1(C(=O)OC(C)(C)C)C(=O)C=CC1CC(=O)OC
Reaction #74824
compound ( 2-a )
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC(C)(C)C)C(=O)C=CC1CC(=O)OC
Reaction #74825
compound ( 2-b )
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC(C)(C)C)C(=O)C=CC1CC(=O)OC
Reaction #74826
compound ( 2-b )
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCC1(C(=O)OC)C(O)CCC1CC(=O)OC
Reaction #74827
compound ( 1-a )
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCC1(C(=O)OC(C)(C)C)C(O)CCC1CC(=O)OC
Reaction #74828
compound ( 1-a )
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)C=CCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #75240
4-(4-Acetyl-8-hydroxytridec-6-en-1-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(C)(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #75242
4-(4-Acetyl-8-hydroxy-8-methyltridecyl)benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
C1=C2CCCOC2CCC1
Reaction #160822
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1(O)C=C(C)C(=O)C=C1C
Reaction #173770
DOI: 10.1039/C8SC04228D
COc1ccc2c(OC3CC4C(=O)NC5(C(=O)O)CC5C=CCCCCN(C)C(=O)C4C3)cc(-c3csc(C4CCCCC4)n3)nc2c1C
Reaction #185264
DOI: 10.1039/C8SC04228D
O=C1CC(=O)NC(=O)N1
Reaction #195808
DOI: 10.1039/C8SC04228D
COc1ccc2c(OC3CC4C(=O)NC5(C(=O)O)CC5C=CCCCCN(C)C(=O)C4C3)cc(-c3cccc(C(C)C)n3)nc2c1C
Reaction #197843
DOI: 10.1039/C8SC04228D
O=C(O)C1CC(=C2CCCN(c3ccccc3)C2=O)c2ccc(Cl)cc2N1
Reaction #206487
DOI: 10.1039/C8SC04228D
CCC#CCC1C(=O)C=CC1CC(=O)OC
Reaction #212604
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)N(C)[C@@H](CCCNC(=N)N)C(=O)C(N)(C(=O)c2ccccc2)C2=CC(CC(=O)OCc3ccccc3)C(=O)N(c3ccccc3)CC2)cc1
Reaction #217052
title compound ( 17 )
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1(c2ccc(-c3ccccc3)cc2)CC2C(=O)NC3(C(=O)O)CC3C=CCCCN(S(=O)(=O)c3ccccc3[N+](=O)[O-])CC(NC(=O)OC(C)(C)C)C(=O)N2C1
Reaction #229250
DOI: 10.1039/C8SC04228D
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