1,2,3-trimethylbenzene

O=[N+]([O-])c1ccccc1N1CCCc2ccccc21
Reaction #4126
product
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1cc(Br)ccc1N1CCCc2ccccc21
Reaction #4139
product
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1ccccc1N1CCCc2ccccc21
Reaction #4184
product
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1cc(Br)ccc1N1CCCc2ccccc21
Reaction #4197
product
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1ccccc1N1CCCc2ccccc21
Reaction #62655
product
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=[N+]([O-])c1cc(Br)ccc1N1CCCc2ccccc21
Reaction #62668
product
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=[N+]([O-])c1ccccc1N1CCCc2ccccc21
Reaction #63410
product
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=[N+]([O-])c1cc(Br)ccc1N1CCCc2ccccc21
Reaction #63418
product
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=[N+]([O-])c1ccccc1N1CCCc2ccccc21
Reaction #176003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(PCl)cc(C)c1C
Reaction #224116
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc2c(c(C)c1C)C(=O)C(C)C2
Reaction #444851
2,5,6,7-Tetramethyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
Cc1ccc(C=O)c(C)c1C
Reaction #448477
2,3,4-Trimethylbenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
COC(=O)[C@@H]1CCCN1C(C)=O
Reaction #667006
N-acetylproline methyl ester
Ausbeute 47.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_06
Cc1cc2c(c(C)c1C)C(=O)C(C)C2
Reaction #670778
2,5,6,7-Tetramethyl-1-Indanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
O=[N+]([O-])c1ccccc1N1CCCc2ccccc21
Reaction #1065467
product
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_05
O=[N+]([O-])c1cc(Br)ccc1N1CCCc2ccccc21
Reaction #1065480
product
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_05
Cc1cc2c(c(C)c1C)C(=O)C(C)C2
Reaction #1091734
2,5,6,7-Tetramethyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_04
Cc1cc2c(c(C)c1C)C(=O)C(C)C2
Reaction #1546208
2,5,6,7-Tetramethyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
O=[N+]([O-])c1cc(Br)ccc1N1CCCc2ccccc21
Reaction #1635175
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
O=[N+]([O-])c1ccccc1N1CCCc2ccccc21
Reaction #1639204
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
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