Ähnlichkeitssuche

8579

COc1c(NC2CCC(=Cc3ccccc3)CC2)ccnc1C
Reaction #1103
4-(4-Benzylidenecyclohexylamino)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCCCC=Cc1ccc(Cl)cc1
Reaction #5353
10-(4-chlorophenyl)-dec-9-enoic acid methyl ester
Ausbeute 13.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Cl-]
Reaction #6701
4-methoxybenzyltriphenyl phosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cc(C=Cc3ccccc3)[nH]c2c1
Reaction #11220
( 146 )
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCOc1ccc(C=Cc2ccc(C=Cc3ccc(OCCCCCCCCCCCCCCC)cc3)cc2)cc1
Reaction #47223
1,4-bis(4′-pentadecanoxystyryl)benzene
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
C(=C1CCN(Cc2ccccc2)CC1)c1ccccc1
Reaction #81942
1-benzyl-4-benzylidenepiperidine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C/C(=C/c2ccccc2)CC[C@@H]1C(=O)N1CCN(c2ccccc2)CC1
Reaction #89767
methyl(1S,2S,5E)-5-benzylidene-2-[(4-phenylpiperazin-1-yl)carbonyl]-cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(=Cc2ccccc2)CC1
Reaction #95967
4-benzylidenecyclohexanone
Ausbeute 120.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Br-]
Reaction #171172
title compound
Ausbeute 156.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCC)c1ccc(C=Cc2ccc(CO)cc2)cc1
Reaction #172525
yellow liquid
Ausbeute 85.6%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C=C(c2ccccc2)C(F)(F)F)cc1
Reaction #193606
DOI: 10.1039/C8SC04228D
Nc1nc2cc(CCc3ccccc3)ccc2c2cccnc12
Reaction #225171
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N(Cc1cccnc1)c1cccc(C=Cc2ccccc2)c1
Reaction #248310
DOI: 10.1039/C8SC04228D
COC(=O)CCCCCCCC=Cc1ccc(Cl)cc1
Reaction #250285
DOI: 10.1039/C8SC04228D
C(=C1CCN(Cc2ccccc2)CC1)c1ccccc1
Reaction #266827
DOI: 10.1039/C8SC04228D
Fc1ccc(C=CC2CCC(C3CCC(CCC4OCCO4)CC3)CC2)cc1
Reaction #279979
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #282270
DOI: 10.1039/C8SC04228D
Fc1ccc(C=Cc2ccc(-c3ccc4ccccc4c3)cc2F)cc1
Reaction #289866
DOI: 10.1039/C8SC04228D
C(=C\c1c[nH]c2cccc(OCc3ccccc3)c12)/c1ccccc1
Reaction #318070
title compound
Ausbeute 197.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1c(C)c(C)c2c(c1C)CC(C)(/C=C\c1ccccc1)O2
Reaction #321437
desired compound
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1
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