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38725

O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
Reaction #51410
2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CNCCN1c1nccnc1OCCOc1cccnc1OCCN(C)C
Reaction #162658
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C2CCCc3cncn32)c(-c2ccccc2)c1
Reaction #164081
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccnc1COc1ccc(C(F)(F)F)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1C[C@H]1CCCO1
Reaction #169941
title compound
Выход 48.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
Reaction #220399
2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1[C@H](CCC=O)CCN1C(=O)OCC
Reaction #432541
trans 1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-propionaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1[C@@H](CCC=O)CCN1C(=O)OCC
Reaction #432543
cis 1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-propionaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
Reaction #498514
2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
Reaction #501018
2-aza-2-benzyl-4-oximino-3-oxo-bicyclo[3,2,1]octane
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
Reaction #520554
2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc2nccc(OC)c2c1N
Reaction #529957
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc2ccnc(Cl)c2c1N
Reaction #529959
title compound
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(N)Cc2cc(OC)cnc2S1
Reaction #529962
title compound
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
Reaction #567930
2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(O)CCC(C#N)(c2ccc(F)nc2)C1
Reaction #599329
crude title compound
Выход 105.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1CS(=O)(=O)c1ccccc1
Reaction #820223
title product
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
Reaction #947393
2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1CS(=O)(=O)c1ccccc1
Reaction #977191
title product
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C2CCCc3cncn32)c(-c2ccccc2)c1
Reaction #1010464
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
Reaction #1052905
2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
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