decane

C=C(CO)c1ccccc1
Reaction #46061
3-hydroxy-2-phenylpropene
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCC
Reaction #70057
normal-decane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCS(=O)c1ccc(NC(=O)C(C)(O)C(F)(F)F)c(Cl)c1Cl
Reaction #190563
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)OC(=O)CC(O)CBr
Reaction #272580
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)C(CO)Nc1nc(Cl)nc2c1S(=O)CC2
Reaction #272950
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
FC(F)(F)c1ccc2c(c1)CC1OC21
Reaction #277460
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
[Br-]
Reaction #294484
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)c1ccccn1.[F][Co][F]
Reaction #304758
cobalt fluoride picolinic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
—
Reaction #344418
54.8
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
—
Reaction #345420
13.6
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
CCCCCCCCCC
Reaction #345421
decane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
CCCCCCCCCC
Reaction #345422
decane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
CCOc1ccccc1C(C)(C)C
Reaction #361121
o-tert-butylphenyl ethyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
C=C1[C@@H]2CC[C@@H](C2)[C@@]1(C)CCC=C(C)C
Reaction #417910
Beta-santalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
—
Reaction #460016
3,4-dihydro-6-(1,1-dimethylethyl)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
CC(C)(C)c1cc(I)c2c(c1)CNC1(O2)C2CC3CC(C2)CC1C3
Reaction #460018
3,4-dihydro-6-(1,1-dimethylethyl)-8-iodospiro[2H-1,3-benzoxazine-2,2'-tricyclo(3.3.1.13,7)decane]
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
OC[C@@H]1O[C@H]1CCc1ccccc1
Reaction #463691
16
收率 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
Cc1ccc2c(c1)CC(=O)N2c1c(F)cccc1Cl
Reaction #469689
N-(2′-chloro-6′-fluorophenyl)-5-methyloxindole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
C=CCOP(=O)(OCC=C)OC[C@@](C)(CCc1ccc(C(=O)CCCCc2ccccc2)n1C)NC(=O)OC(C)(C)C
Reaction #510106
title compound
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C(=C\c1ccccc1)/c1ccccc1
Reaction #516789
trans-stilbene
收率 86.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
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