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215701

Nc1cccc(-c2cccnc2)c1
Reaction #78092
2p
Выход 95.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC=CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81459
title compound
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(Oc3c(F)c(F)c(C(F)(F)F)c(F)c3F)=CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81460
title compound
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1CC[C@@]2(C)[C@@H](CC[C@@H]3[C@@H]2CC[C@]2(C)C(c4cccnc4)=CC[C@@H]32)C1
Reaction #81463
3α-Acetoxy-17-(3-pyridyl)-5α-androst-16-ene
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81467
17-(3-Pyridyl)androsta-5,16-dien-3β-ol
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(-c2cccnc2)nc1C(=O)O
Reaction #165746
product
Выход 83.4%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)c(-c2cccnc2)c1
Reaction #184170
DOI: 10.1039/C8SC04228D
Brc1cccc(-c2cccnc2)n1
Reaction #203284
DOI: 10.1039/C8SC04228D
CC12CCC=CC1=CCC1C2CCC2(C)C(c3cccnc3)=CCC12
Reaction #207104
DOI: 10.1039/C8SC04228D
N#Cc1ccc2c(c1)ncn2-c1cccc(-c2cccnc2)c1
Reaction #208032
DOI: 10.1039/C8SC04228D
FC(F)(F)c1cc(-c2cccnc2)c2c(c1)ncn2-c1ccccc1
Reaction #233869
DOI: 10.1039/C8SC04228D
CSc1nncc(-c2ccc(F)c(-c3cccnc3)c2)n1
Reaction #237895
DOI: 10.1039/C8SC04228D
CC1CN(c2ncc(Cl)cc2Cl)CCN1c1nc2cc(C(F)(F)F)cc(-c3cccnc3)c2[nH]1
Reaction #240950
DOI: 10.1039/C8SC04228D
COc1cc(-c2cccnc2)ccc1C
Reaction #244921
DOI: 10.1039/C8SC04228D
CCB(CC)c1cccnc1
Reaction #244933
DOI: 10.1039/C8SC04228D
CC12CCC(O)CC1=CCC1C2CCC2(C)C(c3cccnc3)=CCC12
Reaction #248123
DOI: 10.1039/C8SC04228D
Nc1ccc(F)c(-c2cccnc2)c1F
Reaction #248161
DOI: 10.1039/C8SC04228D
Oc1cccc(-c2cccnc2)c1
Reaction #258573
DOI: 10.1039/C8SC04228D
Nc1cc(-c2cccnc2)cc(-n2cccn2)c1[N+](=O)[O-]
Reaction #274945
DOI: 10.1039/C8SC04228D
OCCc1ccc(-c2cccnc2)cc1
Reaction #298556
DOI: 10.1039/C8SC04228D
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