CH2═CHCH2CH2OH

C=CCCOC(=O)C(C)Cl
Reaction #6669
CH3CHClCOOCH2CH2CH═CH2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCCO[Si](C)(C)C(C)(C)C
Reaction #80852
product
المردود 56.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=CCCCCCCCC(=O)OCCC=C
Reaction #90835
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=CCCOC1CCCCC1O
Reaction #160798
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1OCCC1CCCCO
Reaction #178587
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCCOC1CCCCO1
Reaction #191786
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCCOc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #194244
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1c(O)c2c(-c3ccc(C=CCCO)cc3)csc2[nH]c1=O
Reaction #201707
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCCOc1cncc(N)n1
Reaction #247168
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCCOC1CCCCCC=C1Br
Reaction #294369
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=CCCOc1ccc(-c2ccc(OCCCCCCCC)cc2)c(F)c1F
Reaction #296314
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=CCCO[Si](C)(C)C(C)(C)C
Reaction #299351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)c1ccc([N+](=O)[O-])cc1C=CCCO
Reaction #325662
4-(2-tert-Butyl-5-nitro-phenyl)-but-3-en-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=CCCOCCCCCCBr
Reaction #398404
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Brc1ccc(C2CC(Br)CCO2)cc1
Reaction #425724
title compound
المردود 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
C=CC(C)O[C@H](C=C)CO
Reaction #468900
27
المردود 81577.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
C=CCCO[Si](C)(C)C(C)(C)C
Reaction #482012
product
المردود 56.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
OCC/C=C/c1ccc(Cl)cc1
Reaction #551203
title compound
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_10
C=CCCOCC(=O)O
Reaction #566329
title compound
المردود 126.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CC(C)(C)c1ccc([N+](=O)[O-])cc1C=CCCO
Reaction #644516
4-(2-tert-Butyl-5-nitro-phenyl)-but-3-en-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
الصفحة 1التالي