azide

CNN=NCCN=NNC
Reaction #2786
off-white solid
المردود 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(C)(CN=[N+]=[N-])NC(=O)OCc1ccccc1
Reaction #5652
1-Azido-2-(benyloxycarbonylamino)-2-methylbutane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
[N-]=[N+]=NC(COCc1ccccc1)CN1C(=O)c2ccccc2C1=O
Reaction #65324
2-Benzyloxymethyl-2-azido-1-phthalimido-ethane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C)(C)NC(=O)CN1C(=O)C(N=[N+]=[N-])CC(c2ccccc2)c2ccccc21
Reaction #81407
foam
المردود 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Nc1cc(-c2ccncc2)n[nH]c1=O
Reaction #96014
4-Amino-6-(4-pyridinyl)-3(2H)-pyridazinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CC(=O)OC[C@H]1O[C@H](O[C@@H]2[C@H](OC(C)=O)[C@@H](O[C@@H]3[C@@H](OCCCn4cc(CO[C@H]5CC[C@@]6(C)C(CC[C@H]7[C@@H]8CC[C@H]([C@H](C)CCCC(C)C)[C@@]8(C)CC[C@@H]76)C5)nn4)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]3OC(C)=O)O[C@H](COC(C)=O)[C@H]2OC(C)=O)[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #162019
triazole
المردود 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)[Si](C)(C)O[C@]1(C)CCC[C@H](N)[C@H]1O
Reaction #162165
oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
[N-]=[N+]=NCCc1ccc(CO)cc1
Reaction #164460
4-(2-azidoethyl)-benzyl alcohol
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(CNC(=O)OC(C)(C)C)c1ccc(Cl)cc1
Reaction #169590
methyl 3-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)propanoate
المردود 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CCCC(C(OCCN=[N+]=[N-])c2cccc(F)c2F)C1
Reaction #172988
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(C(=O)CN=[N+]=[N-])cc1
Reaction #173053
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1c(CN=[N+]=[N-])c(=O)c2ccc(Cl)cc2n1-c1ccccc1
Reaction #173221
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[N-]=[N+]=NC1CC(C(=O)N2CCCC2C(=O)NCC2CCCN(CC3CCCCC3)C2)N(C(=O)CC(c2ccccc2)(c2ccccc2)c2ccccc2)C1
Reaction #173824
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(=NOCCN=[N+]=[N-])c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #173860
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[N-]=[N+]=NCc1c(F)cccc1F
Reaction #175065
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)OCC(CCN=[N+]=[N-])O1
Reaction #175370
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[N-]=[N+]=NCc1nc2cccc(Cl)c2nc1-c1ccccc1C(F)(F)F
Reaction #175894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[N-]=[N+]=NCc1cccnc1N1CCOCC1
Reaction #176286
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nnc(CN=[N+]=[N-])o1
Reaction #176388
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[N-]=[N+]=NCC1Cc2cccc(-c3c(Cl)cccc3Cl)c2O1
Reaction #176923
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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