Busqueda de Subestructura

606011

Nc1cnccc1OCc1ccccc1
Reaction #72283
4-(benzyloxy)pyridin-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cnccc1OCc1ccccc1
Reaction #72387
4-(benzyloxy)pyridine-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N(c1cnccc1OCc1ccccc1)S(C)(=O)=O
Reaction #72388
N-(4-(benzyloxy)pyridin-3-yl)-N-(methylsulfonyl)methane sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCOc1ccncc1[N+](=O)[O-]
Reaction #157046
tert-butyl 2-(3-nitropyridin-4-yloxy)ethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccncc1[N+](=O)[O-]
Reaction #182390
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cnccc1OCc1ccc2c(c1)OCO2
Reaction #184426
DOI: 10.1039/C8SC04228D
COCCOc1nc(C)cc(OCC(F)(F)F)c1N
Reaction #187641
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cnccc1OCc1ccc(C(F)(F)F)cc1
Reaction #193104
DOI: 10.1039/C8SC04228D
COCCOc1nc(C)cc(OCC(F)(F)F)c1[N+](=O)[O-]
Reaction #242612
DOI: 10.1039/C8SC04228D
C=CCNc1ccncc1[N+](=O)[O-]
Reaction #257716
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(COc2cc(Nc3cnc(C#N)cn3)ncc2N)CC1
Reaction #258819
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cnccc1OCc1cccnc1
Reaction #277479
DOI: 10.1039/C8SC04228D
Nc1cnccc1OCc1ccccc1
Reaction #306507
4-(benzyloxy)pyridin-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cnccc1OCc1ccccc1
Reaction #306600
4-(benzyloxy)pyridine-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N(c1cnccc1OCc1ccccc1)S(C)(=O)=O
Reaction #306601
N-(4-(benzyloxy)pyridin-3-yl)-N-(methylsulfonyl)methane sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnccc1NCC1(c2ccc(OCCCN3CCCC3)cc2)CCOCC1
Reaction #360226
title compound
Rendimiento 38.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)ncc([N+](=O)[O-])c1OC(C)(C)C
Reaction #395853
DOI: 10.1039/C8SC04228D
Cc1c(C2CC2CC#N)ncc([N+](=O)[O-])c1O
Reaction #396843
DOI: 10.1039/C8SC04228D
Cc1c(C2CC2CC#N)ncc([N+](=O)[O-])c1OC(C)(C)C
Reaction #406525
DOI: 10.1039/C8SC04228D
O=C(O)CCc1ccc(CNc2ccncc2[N+](=O)[O-])o1
Reaction #462819
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
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