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5125

C=CCc1cc(C=C2SC(=S)NC2=O)cc(CC=C)c1O
Reaction #3045
5-[(3,5-di-2-propenyl-4-hydroxyphenyl)-methylene]-2-thioxo-4-thiazolidinone
Ausbeute 94.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1cc(C(=O)OC)cc(CC=C)c1O
Reaction #6025
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1cc(C(=O)OC)cc(CC=C)c1O[Si](C)(C)C(C)(C)C
Reaction #6026
title compound
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C(=O)OC)cc(CCC)c1O[Si](C)(C)C(C)(C)C
Reaction #6027
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1cc(C=C2SC(=S)NC2=O)cc(CC=C)c1O
Reaction #554382
5-[(3,5-di-2-propenyl-4-hydroxyphenyl)methylene]-2-thioxo-4-thiazolidinone
Ausbeute 94.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCc1c(O)c(CC=C(C)C)c(O)c(C(=O)C(C)C)c1O
Reaction #654385
{3,5-bis(3-methyl-2-butenyl)-2,4,6-trihydroxyphenyl} (2-propyl) ketone
Ausbeute 7.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCc1c(O)c(CC=C(C)C)c(O)c(C(=O)CC(C)C)c1O
Reaction #654387
{3,5-bis(3-methyl-2-butenyl)-2,4,6-trihydroxyphenyl} (2-methylpropyl) ketone
Ausbeute 17.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCc1c(O)c(CCC(C)C)c(O)c(C(=O)CC(C)C)c1O
Reaction #654390
product ( 37 )
Ausbeute 86.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCOc1c(CC=C(C)C)c(C)c(C(=O)CC(C)C)c(O)c1CC=C(C)C
Reaction #654393
{3,5-bis(3-methyl-2-butenyl)-2-hydroxy-6-methyl-4-(3-methyl-2-butenyloxy)phenyl}(2-methylpropyl) ketone
DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1cc(C(=O)OC)cc(CC=C)c1OC
Reaction #726132
3,5-Diallyl-4-methoxybenzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1cc(C(=O)OC)cc(CC=C)c1O
Reaction #1579784
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1cc(C(=O)OC)cc(CC=C)c1O[Si](C)(C)C(C)(C)C
Reaction #1579785
title compound
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C(=O)OC)cc(CCC)c1O[Si](C)(C)C(C)(C)C
Reaction #1579786
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)c1c(O)c(CC=C(C)C)c(O)c(CC=C(C)C)c1O
Reaction #1615216
desired compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2oc3c(CC=C(C)C)c(O)c(CC=C(C)C)c(O)c3c(=O)c2OC)cc1F
Reaction #1615217
desired compound
Ausbeute 32.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1c(O)c(CC=C(C)C)c(O)c(CC=C(C)C)c1O
Reaction #1615218
desired compound
Ausbeute 38.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCc1c(O)c(CC=C(C)C)c2oc(-c3ccc(F)c(F)c3)cc(=O)c2c1O
Reaction #1615219
desired compound
Ausbeute 2.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCc1c(O)c(CC=C(C)C)c2oc(-c3ccc(Cl)c(F)c3)cc(=O)c2c1O
Reaction #1615220
desired compound
Ausbeute 3.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1c(O)c(CC=C(C)C)c(O)c(CC=C(C)C)c1O
Reaction #1615221
desired compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCc1c(O)c(CC=C(C)C)c2oc(-c3ccc(F)c(F)c3)c(C)c(=O)c2c1O
Reaction #1615222
desired compound
Ausbeute 1.2%DOI: 10.6084/m9.figshare.5104873.v1
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