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N=C(NC(=O)OCc1ccccc1)c1ccc(CN)cc1

[N-]=[N+]=NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1
Reaction #952
4-(benzyloxycarbonylamidino) benzyl azide
DOI: 10.6084/m9.figshare.5104873.v1
N=C(NC(=O)OCc1ccccc1)c1ccc(CN)cc1
Reaction #953
4-aminomethyl-1-(N-benzyloxycarbonylamidino)benzene
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)N=[N+]=[N-]
Reaction #11067
intermediate
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)NCC
Reaction #11084
26b
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)NC(C)C
Reaction #11085
27a
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H]1C[C@@H](C(=O)NCc2ccc(C(=N)NC(=O)OCc3ccccc3)cc2)n2c1ncc(N(CC=C)C(=O)OCc1ccccc1)c2=O
Reaction #11087
intermediate 28e
Ausbeute 20.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #11089
EtOAc hexanes
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)CC(=O)OC(C)(C)C
Reaction #11100
intermediate 38d
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)CC(=O)O
Reaction #11101
intermediate 39a
Ausbeute 102.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)CC(=O)Nc1ccccc1
Reaction #11102
intermediate 40a
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)CC(=O)N1CCCCC1
Reaction #11103
intermediate 41a
Ausbeute 72.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@]2(C)NC=O
Reaction #11104
intermediate 42a
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(NC(=O)OCc1ccccc1)c1ccc(CN)cc1
Reaction #198468
DOI: 10.1039/C8SC04228D
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)C(C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)CC2(C)CC(=O)O
Reaction #232312
DOI: 10.1039/C8SC04228D
CCOC(C(=O)NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1)c1c(F)cc(O)cc1F
Reaction #252487
DOI: 10.1039/C8SC04228D
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)C(C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)CC2(C)N=[N+]=[N-]
Reaction #271421
DOI: 10.1039/C8SC04228D
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)C(C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)CC2(C)CC(=O)N1CCCCC1
Reaction #283354
DOI: 10.1039/C8SC04228D
CCOC(C(=O)NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1)c1c(F)cc(OCCN2CCOCC2)cc1F
Reaction #368412
DOI: 10.1039/C8SC04228D
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)C(C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)CC2(C)CC(=O)Nc1ccccc1
Reaction #396265
DOI: 10.1039/C8SC04228D
Cl
Reaction #408453
DOI: 10.1039/C8SC04228D
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