platinum chloride

[Pt]
Reaction #312595
platinum
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
C=C(C)C(=O)OCCC[Si](Cl)(Cl)Cl
Reaction #371899
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC1=C(CC)c2nc1c(CC)c1[nH]c(cc3nc(cc4c(CC)c(CC)c(c2Br)n4CC)C=C3)c(CC)c1CC.[Pt]
Reaction #563724
Platinum (5-Bromo Octaethylporphine)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_12
Fc1ccc(C2CCCO2)c(Br)c1
Reaction #645317
title compound
Yield 77.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CO[Si](CCCOCC1CO1)(OC)OC
Reaction #749985
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Fc1ccc(C2CCCO2)c(Br)c1
Reaction #756949
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC[Si](C)(C)CCCCc1ccc(Br)cc1
Reaction #784530
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C1CC2CC2(c2cccc3ccccc23)C1
Reaction #1183909
desired compound
Yield 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
O=C1CC2CC2(c2ccc3ccccc3c2)C1
Reaction #1183919
desired compound
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
COc1ccc(C2CC(C)C(=O)NC2C)cc1
Reaction #1621985
3,6-dimethyl-5-(4-methoxyphenyl)-3,4,5,6-tetrahydro-2-pyridone
Yield 38.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_02
COc1ccc(C2CC(C)C(=O)NC2C)cc1
Reaction #2223995
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)