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Cc1cnc(O)c2cccc(N)c12

Cc1cnc(O)c2cccc(N)c12
Reaction #10687
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(O)c2cccc(N[C@H]3CC[C@H](N)CC3)c12.Cl
Reaction #10688
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ncc(C(=O)O)c2c([N+](=O)[O-])cccc12
Reaction #383960
DOI: 10.1039/C8SC04228D
Cc1cnc(O)c2cccc(NC3CCC(N)CC3)c12
Reaction #762329
DOI: 10.1039/C8SC04228D
Cc1cnc(O)c2cccc(N)c12
Reaction #2229392
DOI: 10.1039/C8SC04228D
CCOc1ncc2c(=O)c3cccn3c3cccc1c23
Reaction #2251228
4-ethoxy-7-oxo-7H-indolizino[7,6,5-de]isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ncc(C(=O)O)c2c([N+](=O)[O-])cccc12
Reaction #2251229
4-carboxy-1-ethoxy-5-nitroisoquinoline
Rendimiento 100.7%DOI: 10.6084/m9.figshare.5104873.v1