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69666

CC1(C)Oc2ccc(Br)cc2C2(COC(N)=N2)C12COC2
Reaction #682073
6′-bromo-2′,2′-dimethyldispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(Br)cc2[C@@]2(COC(N)=N2)C12CC2
Reaction #682097
(4′R)-6′-bromo-2′,2′-dimethyldispiro[cyclopropane-1,3′-chromene-4′,4″-[1,3]oxazol]-2″-amine
Ausbeute 40.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(Br)cc2C2(COC(N)=N2)C12COC2
Reaction #960926
6′-bromo-2′,2′-dimethyldispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(Br)cc2[C@@]2(COC(N)=N2)C12CC2
Reaction #960951
(4′R)-6′-bromo-2′,2′-dimethyldispiro[cyclopropane-1,3′-chromene-4′,4″-[1,3]oxazol]-2″-amine
Ausbeute 40.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cncc(-c2ccc3c(c2)[C@@]2(CCC3)N=C(N)OCC2(F)F)c1
Reaction #1612332
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CCC(F)(F)c3ccc(-c4cncc(Cl)c4)cc32)C(F)(F)CO1
Reaction #1612333
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CCC(F)(F)c3ccc(-c4cncc(F)c4)cc32)C(F)(F)CO1
Reaction #1612334
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cncc(-c2ccc3c(c2)[C@@]2(CCC3(F)F)N=C(N)OCC2(F)F)c1
Reaction #1612335
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CCc3ccc(-c4cncnc4)cc32)C(F)(F)CO1
Reaction #1612336
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CCc3ccc(-c4cc(Cl)cc(Cl)c4)cc32)C(F)(F)CO1
Reaction #1612337
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CCc3ccc(-c4cncc(Cl)c4)cc32)C(F)(F)CO1
Reaction #1612338
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(-c2ccc3c(c2)[C@@]2(CC3)N=C(N)OCC2(F)F)c1
Reaction #1612339
title compound
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cncc(-c2ccc3c(c2)[C@@]2(CC3)N=C(N)OCC2(F)F)c1
Reaction #1612340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CCOc3ccc(-c4cc(Cl)cc(Cl)c4)cc32)C(F)(F)CO1
Reaction #1612352
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CCOc3ccc(-c4cncnc4)cc32)C(F)(F)CO1
Reaction #1612353
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cncc(-c2ccc3c(c2)[C@@]2(CCO3)N=C(N)OCC2(F)F)c1
Reaction #1612354
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CC(c3ccccc3)Oc3ccc(-c4cncc(Cl)c4)cc32)C(F)(F)CO1
Reaction #1612355
title compound
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cncc(-c2ccc3c(c2)[C@@]2(CC(c4ccccc4)O3)N=C(N)OCC2(F)F)c1
Reaction #1612356
title compound
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CC(c3ccccc3)Oc3ccc(-c4cncnc4)cc32)C(F)(F)CO1
Reaction #1612357
title compound
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CC(c3ccccc3)Oc3ccc(-c4cc(Cl)cc(Cl)c4)cc32)C(F)(F)CO1
Reaction #1612358
title compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
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