1-oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine

CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220812
title compound
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1(C)CC(O)CC(C)(C)N1OC1CCCCCCC1
Reaction #220821
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220840
title compound
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220841
title compound
收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220842
1-Cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-ol
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220843
1-Cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-ol
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220844
1-Cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-ol
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)(O)CON1C(C)(C)CC(O)CC1(C)C
Reaction #233322
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(O)CON1C(C)(C)CC(O)CC1(C)C
Reaction #239356
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #244325
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CON1C(C)(C)CC(O)CC1(C)C
Reaction #251017
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)CC(O)CC(C)(C)N1OC1C=CCCCCC1
Reaction #259971
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(O)CON1C(C)(C)CC(O)CC1(C)C
Reaction #282193
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(C)CC(O)CC(C)(C)N1OCc1ccccc1
Reaction #381535
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CON1C(C)(C)CC(O)CC1(C)C
Reaction #403691
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1(C)CC(O)CC(C)(C)N1OC1C=CCCC1
Reaction #409974
white solid
收率 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Cc1cccc(CON2C(C)(C)CC(O)CC2(C)C)c1
Reaction #409975
white solid
收率 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Cc1ccc(CON2C(C)(C)CC(O)CC2(C)C)cc1
Reaction #409976
white solid
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CC1(C)CC(O)CC(C)(C)N1OCc1ccccc1
Reaction #409979
white solid
收率 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CC(ON1C(C)(C)CC(O)CC1(C)C)c1ccccc1
Reaction #409980
off-white solid
收率 45.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
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