Substructure Search

4081

CCOP(=O)(COCOCn1cc(C)c(=O)[nH]c1=O)OCC
Reaction #1647
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(O)c2ncn(COC(CO)CO)c2n1
Reaction #3723
ganciclovir
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cn(CCCO[Si](C)(C)C(C)(C)C)c(=O)[nH]c1=O
Reaction #40940
title compound
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cn(CCCO)c(=O)[nH]c1=O
Reaction #40941
title compound
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cn(CCC=O)c(=O)[nH]c1=O
Reaction #40942
title compound
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cn(CCCCO[Si](C)(C)C(C)(C)C)c(=O)[nH]c1=O
Reaction #40943
title compound
Yield 23.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cn(CCCC=O)c(=O)[nH]c1=O
Reaction #40944
title compound
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1cccs1
Reaction #41030
title compound
Yield 59.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3F)C2)cc1-c1cccs1
Reaction #41033
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1C(F)(F)F
Reaction #41034
title compound
Yield 51.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1C(F)(F)F
Reaction #41035
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cn(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)c(=O)[nH]c1=O.Cl
Reaction #41038
title compound
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cn(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)c(=O)[nH]c1=O.Cl
Reaction #41040
title compound
Yield 48.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1cccnc1F
Reaction #41049
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1ccc(F)nc1F
Reaction #41062
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1cccnc1F
Reaction #41078
title compound
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(F)c(-c2cn(CCCN3C[C@@H]4C[C@]4(c4ccc(C(F)(F)F)cc4)C3)c(=O)[nH]c2=O)c1.Cl.Cl
Reaction #41083
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cn(CCCN3C[C@@H]4C[C@]4(c4ccc(C(F)(F)F)cc4)C3)c(=O)[nH]c2=O)c(F)n1
Reaction #41088
title compound
Yield 40.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=c1[nH]c(=O)n(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1cccnc1F
Reaction #41093
title compound
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1c(C=O)c(=O)n(C)c(=O)n1C
Reaction #70974
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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