levulenic acid

O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #1612
product
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #1681
product
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #2186
product
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #2227
product
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)C=Cc1ccc(Cl)cc1
Reaction #2285
product
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN(C(C)C)C(C)C
Reaction #10852
DIEA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCOCCOC(=O)CCC(C)=O
Reaction #54170
2-Butoxyethyl Levulinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC(C)(C)N=NC(C)(C#N)CCC(=O)O
Reaction #94170
product
Ausbeute 86.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC(CCC(=O)OCCCO)OCCCO
Reaction #161320
3-hydroxypropyl 4-(3-hydroxypropoxy)pentanoate
Ausbeute 5.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(CCC(=O)OCCOCCO)OCCOCCO
Reaction #161321
2-(2-hydroxyethoxy)ethyl 4-(2-(2-hydroxyethoxy)ethoxy)pentanoate
Ausbeute 23.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc2c3c([nH]c2c1)C1(C)CCC(=O)N1CC3
Reaction #188805
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCOC(=O)CCC(C)=O
Reaction #198144
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(CCC(=O)O)OCCC2=C1Cc1ccccc12
Reaction #212331
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(CCC(=O)O)OCCc2c1[nH]c1ccccc21
Reaction #238108
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)CCC(=O)N(CC(C)C)NC(=O)C(CC(C)C)C(CC=Cc1ccccc1)C(=O)NOC1CCCCO1
Reaction #245235
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)N=NC(C)(C#N)CCC(=O)O
Reaction #280433
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)CCC(=O)N(C)Cc1ccccc1
Reaction #283940
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)CCC(=O)[O-].[Cs+]
Reaction #321746
CESIUM LEVULINATE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC12CCC(=O)N1CCc1c2[nH]c2ccccc12
Reaction #354735
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
CCCCCCCCCCN1C(=O)CCC1C
Reaction #399236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Seite 1Weiter