Teilstruktursuche

84891

CC1C=CC=C(c2ccncc2[N+](=O)[O-])C1
Reaction #160764
(+/−)-4-(5-methylcyclohexa-1,3-dienyl)-3-nitropyridine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(O)C1Br
Reaction #160765
(+/−)-6-bromo-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC=C(c2ccncc2[N+](=O)[O-])C1
Reaction #193608
DOI: 10.1039/C8SC04228D
CC1C=CC=C(c2ccncc2[N+](=O)[O-])C1
Reaction #792427
(+/−)-4-(5-methylcyclohexa-1,3-dienyl)-3-nitropyridine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC=C(c2ccncc2[N+](=O)[O-])C1
Reaction #966340
(+/−)-4-(5-methylcyclohexa-1,3-dienyl)-3-nitropyridine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(O)C1Br
Reaction #966341
(+/−)-6-bromo-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC=C(c2ccncc2[N+](=O)[O-])C1
Reaction #1610620
(+/−)-4-(5-methylcyclohexa-1,3-dienyl)-3-nitropyridine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(N=[N+]=[N-])C1O
Reaction #1610621
(+/−)-2-azido-6-methyl-4-(3-nitropyridin-4-yl)cyclohex-3-enol
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(O)C1Br
Reaction #1610625
(+/−)-6-bromo-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC=C(c2ccncc2[N+](=O)[O-])C1
Reaction #2007402
(+/−)-4-(5-methylcyclohexa-1,3-dienyl)-3-nitropyridine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(O)C1Br
Reaction #2007403
(+/−)-6-bromo-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC=C(c2ccncc2[N+](=O)[O-])C1
Reaction #2133979
(+/−)-4-(5-methylcyclohexa-1,3-dienyl)-3-nitropyridine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(N=[N+]=[N-])C1O
Reaction #2133980
(+/−)-2-azido-6-methyl-4-(3-nitropyridin-4-yl)cyclohex-3-enol
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(O)C1Br
Reaction #2133984
(+/−)-6-bromo-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC=C(c2ccncc2[N+](=O)[O-])C1
Reaction #2279751
(+/−)-4-(5-methylcyclohexa-1,3-dienyl)-3-nitropyridine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(N=[N+]=[N-])C1O
Reaction #2279752
(+/−)-2-azido-6-methyl-4-(3-nitropyridin-4-yl)cyclohex-3-enol
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(O)C1Br
Reaction #2279756
(+/−)-6-bromo-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(N=[N+]=[N-])C1O
Reaction #2420562
DOI: 10.1039/C8SC04228D