Teilstruktursuche

1247624

CCOC(=O)C1(NC(=O)OC(C)(C)C)CC1
Reaction #65058
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cscn1
Reaction #74571
product
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC(=O)c1ccc(-c2nnc(-c3ccc(OC(F)(F)C(F)(F)F)cc3)o2)cc1
Reaction #88153
4-(5-(4-(perfluoroethoxy)phenyl)-1,3,4-oxadiazol-2-yl)benzoyl azide
Ausbeute 63.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ncn(-c3ccc(OC(F)(F)F)cc3)n2)ccc1C(=O)N=[N+]=[N-]
Reaction #88159
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(N=C=O)CCC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162184
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC2CC(Nc3nc(-c4c[nH]c5ncc(F)cc45)ncc3F)C1C2)N1CCCC1
Reaction #162232
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(N=C=O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172944
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-isocyanato-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-ol
Ausbeute 78.1%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCc1ccc(C(F)(F)F)nc1
Reaction #262094
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cccc2c1CCCC2(N=[N+]=[N-])O[SiH](c1ccccc1)c1ccccc1
Reaction #295586
DOI: 10.1039/C8SC04228D
NC12CC3CC(C1)CC(NC(=O)c1ccccn1)(C3)C2
Reaction #305203
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC(CC1OCCO1)c1ccc(C(F)(F)F)nc1
Reaction #329040
5-(1-azido-2-(1,3-dioxolan-2-yl)ethyl)-2-(trifluoromethyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncc(C(C)N=[N+]=[N-])cn1
Reaction #329047
5-(1-azidoethyl)-2-methylpyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H](C)Cn1c(=O)[nH]c2cnc3ccc(Br)cc3c21
Reaction #331779
titled compound
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn2nc(-c3ccccc3)nc2cc1N
Reaction #382306
DOI: 10.1039/C8SC04228D
CC(C)Oc1ccc(-c2noc(-c3ccc(CN=[N+]=[N-])cc3)n2)cc1Cl
Reaction #398662
DOI: 10.1039/C8SC04228D
COc1ccsc1NC(=O)Nc1cc([N+](=O)[O-])ccc1O
Reaction #410211
product
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccsc1NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #410212
product
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N)c1[N+](=O)[O-]
Reaction #421767
3-methoxy-2-nitrophenylamine
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC1=N[C@@H]2[C@@H](O)[C@H](O)[C@@H](CN=[N+]=[N-])O[C@@H]2S1
Reaction #422675
title compound
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cc([N+](=O)[O-])[nH]n1
Reaction #424019
tert-butyl 5-nitro-1H-pyrazol-3-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
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