بحث البنية الفرعية

C1CCN(C1)CCCl.Cl

c1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1
Reaction #1176
brown oil
المردود 92.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(OCCN2CCCC2)c1[N+](=O)[O-]
Reaction #7045
1-[2-(3-Methyl-2-nitrophenoxy)-ethyl]-pyrrolidine
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(OCCN2CCCC2)c1
Reaction #45919
3-(2-pyrrolidin-1-yl-ethoxy)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)(Cl)C(=O)N1CCC[C@H]1C(=O)O
Reaction #50050
N-(2,2-dichloropropionyl)proline
المردود 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)(Cl)C(=O)N1CCC[C@H]1C(=O)O
Reaction #50054
2,2-dichloropropionyl-L-proline
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccc3nnc(CNc4ccnc5cc(OCCN6CCCC6)cnc45)n3n2)cc1
Reaction #68473
N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7-(2-(pyrrolidin-1-yl)ethoxy)-1,5-naphthyridin-4-amine
المردود 22.2%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1C=NOCCN1CCCC1)OCO2
Reaction #70964
1-(5-bromo-1,3-benzodioxol-4-yl)-N-[2-(pyrrolidin-1-yl)ethoxy]methanimine
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)c1ccc(OCCN2CCCC2)cc1Cl
Reaction #94887
1-{2-Chloro-4-[2-(N-pyrrolidinyl)ethoxy]-phenyl}-1-butanone
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc2ncccc2cc1Cc1cnc2ccc(-c3cnn(CCN4CCCC4)c3)nn12
Reaction #156435
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1(CO)CCCN1
Reaction #184500
DOI: 10.1039/C8SC04228D
CN(C)CC1(C(N)=O)CCCN1
Reaction #211638
DOI: 10.1039/C8SC04228D
COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OCC1CCCN1C(=O)CCl
Reaction #255069
DOI: 10.1039/C8SC04228D
NC(=O)C1(Cc2ccccc2)CCCN1
Reaction #270995
DOI: 10.1039/C8SC04228D
C=CCC12CCCN1C(C(Cl)(Cl)Cl)OC2=O
Reaction #277539
DOI: 10.1039/C8SC04228D
COCC12CCCN1C(C(Cl)(Cl)Cl)OC2=O
Reaction #297360
DOI: 10.1039/C8SC04228D
c1ccc(-c2ccc3nnc(CNc4ccnc5cc(OCCN6CCCC6)cnc45)n3n2)cc1
Reaction #306264
N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7-(2-(pyrrolidin-1-yl)ethoxy)-1,5-naphthyridin-4-amine
المردود 22.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]12CCCN1[C@@H](C(Cl)(Cl)Cl)OC2=O
Reaction #337973
oxazolidinone
المردود 63.4%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@]12CCCN1[C@@H](C(Cl)(Cl)Cl)OC2=O
Reaction #337974
oxazolidinone
المردود 46.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]12CCCN1[C@@H](C(Cl)(Cl)Cl)OC2=O
Reaction #337975
oxazolidinone
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@H](C(Cl)(Cl)Cl)N2CCC[C@@]12Cc1ccccc1
Reaction #337976
oxazolidinone
المردود 32.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي