子结构搜索

5104

CCC[C@H](N)C(=O)NC1CCN(c2ccn3c(=O)c(C(=O)O)ccc3c2)C1
Reaction #1942
amino acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2cc(N3CCN(C)CC3)ccn2c1=O
Reaction #1943
title compound
收率 106.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(CC)c2cc(N3CCNC(C)C3)ccn2c1=O
Reaction #1947
title compound
收率 100.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(CC)c2cc(N3CCN(C)CC3)ccn2c1=O
Reaction #1949
title compound
收率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(NC)c2cc(N3CCN(C)CC3)c(F)cn2c1=O
Reaction #1963
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CC[C@@H]([C@H](C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1972
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CC[C@H]([C@@H](C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1973
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)cn2c(=O)c(C(=O)O)c(N3CCC(C(C)N)C3)c(C3CC3)c12.Cl
Reaction #1974
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CCC(N3CCCCC3)CC2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12
Reaction #1975
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CCN(c3ccccn3)CC2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12
Reaction #1976
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CCC(C(C)(C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1977
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(N)C1CCN(c2c(F)cn3c(=O)c(C(=O)O)cc(C4CC4)c3c2C)C1.Cl
Reaction #1978
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C2CC2)c2c(C)c(CC(=O)OC(c3ccccc3)c3ccccc3)c(F)cn2c1=O
Reaction #1995
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2cc(N=[N+]=[N-])ccn2c1=O
Reaction #77188
solid
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2cc(Oc3cccc([N+](=O)[O-])c3)ccn2c1=O
Reaction #77190
solid
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2cc(-c3ccc(OC)cc3)ccn2c1=O
Reaction #77192
solid
收率 52.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C2CC2)c2c(C)c(Cl)c(F)cn2c1=O
Reaction #402902
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(C2CC2)c2c(C)c(Cl)ccn2c1=O
Reaction #1148618
ethyl 8-chloro-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C2CC2)c2c(C)c(-c3ccc4c(c3)CNC4C)ccn2c1=O
Reaction #1148619
ethyl 1-cyclopropyl-9-methyl-8-(1-methylisoindoline-5-yl)-4-oxo-4H-quinolizine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C2CC2)c2c(C)c(Cl)ccn2c1=O
Reaction #1148625
ethyl 8-chloro-1-cyclopropyl-9-methoxy-4-oxo-4H-quinolizine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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