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2416

C=CCCC(=O)Nc1cccc(C(=O)OC)c1
Reaction #2430
oil
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(C(=O)O)C(O)CC(CCCCCCCCCCC)OC1CCCCO1
Reaction #6148
2-allyl-3-hydroxy-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCC(=O)O
Reaction #55587
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCC(C)=O
Reaction #55588
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC=CC(=O)O
Reaction #56092
2-tridecenoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC=CCCCCC(=O)O
Reaction #56096
6-undecenoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC=CCCCCCCC(=O)O
Reaction #56098
8-tetradecenoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCC(=O)O
Reaction #56099
7-octenoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCC(=O)N1C(=O)OC[C@H]1Cc1ccccc1
Reaction #69345
1a
Ausbeute 99498.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCC(=O)O[C@@H](CNC(=O)[C@@H](CC=C)CC(=O)OC(C)(C)C)c1ccccc1
Reaction #69349
desired product
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCC(=O)N[C@@H](CO)c1ccccc1
Reaction #69352
product
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCC(=O)OCc1ccc(OC(=O)CCC=C)c(C(CCN(C(C)C)C(C)C)c2ccccc2)c1
Reaction #78876
(±)-pent-4-enoic acid 2-(3-diisopropyl amino-1-phenylpropyl)-4-(pent-4-enoyloxymethyl)-phenyl ester
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCC(=O)N1C(=O)OC[C@H]1Cc1ccccc1
Reaction #84678
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCC(=O)OCCC=C
Reaction #90835
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCC(=O)NCCC=C
Reaction #90836
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCCNC(=O)CCCC=C
Reaction #90837
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCOC(=O)CCCCCC=C
Reaction #90838
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCC(=O)Cl
Reaction #164092
6-Heptenoyl Chloride
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCC(=O)OC(C)(C)C
Reaction #173954
DOI: 10.1039/C8SC04228D
C=CCCC(O)(CCC=C)c1cccc(F)c1F
Reaction #175000
DOI: 10.1039/C8SC04228D
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