بحث البنية الفرعية

35003

c1ccc(CN2CC[C@H](N3CCCC3)C2)cc1
Reaction #42053
objective compound
المردود 69.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cc2nc3ccccc3[nH]2)cc1)N1CCC(N2CCCC2)C1
Reaction #242904
DOI: 10.1039/C8SC04228D
C1CCN(C2CCNC2)C1
Reaction #246730
DOI: 10.1039/C8SC04228D
Cl
Reaction #279487
DOI: 10.1039/C8SC04228D
Cl.c1ccc2c(c1)ncn2-c1ccc(CN2CC[C@H](N3CCCC3)C2)cc1
Reaction #632482
title product
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(F)cc1)N1CC[C@H](N2CCCC2)C1
Reaction #632484
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(Cc2ccc(CN3CCC(N4CCCC4)C3)cc2)nc2ccccc21
Reaction #770037
DOI: 10.1039/C8SC04228D
c1ccc(CN2CCC(N3CCCC3)C2)cc1
Reaction #912673
DOI: 10.1039/C8SC04228D
O=C1[C@H](Br)CCN1C1CCN(Cc2ccccc2)C1
Reaction #943133
(R)-(1′-benzyl-3-bromo-[1,3′]bipyrrolidinyl-2-one)
المردود 63.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1[C@H]([P+](c2ccccc2)(c2ccccc2)c2ccccc2)CCN1C1CCN(Cc2ccccc2)C1.[Br-]
Reaction #943134
(R)-(1′-benzyl-2-oxo-[1,3′]bipyrrolidinyl-3-yl)-triphenyl-phosphonium bromide
المردود 78.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc2c(c1)ncn2-c1ccc(C(=O)N2CCC(N3CCCC3)C2)cc1
Reaction #1039176
DOI: 10.1039/C8SC04228D
O=C(c1ccc(Cn2ccc3ccccc32)cc1)N1CC[C@H](N2CCCC2)C1
Reaction #1250264
title product
المردود 14.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)/C=C/C(=O)O.O=C(c1ccc(Cc2nc3ccccc3n2CCO)cc1)N1CC[C@H](N2CCCC2)C1
Reaction #1250271
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cc2nc3ccccc3[nH]2)cc1)N1CC[C@H](N2CCCC2)C1
Reaction #1250274
title compound
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)/C=C/C(=O)O.O=C(c1ccc(Cc2nc3ccccc3n2S(=O)(=O)c2ccccc2)cc1)N1CC[C@H](N2CCCC2)C1
Reaction #1250275
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cn2ccc3ccccc32)cc1)N1CC[C@H](N2CCCC2)C1
Reaction #1250277
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(c1ccc(Cc2ccccc2)cc1)N1CC[C@H](N2CCCC2)C1
Reaction #1250280
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(Cc2ccc(CN3CC[C@H](N4CCCC4)C3)cc2)nc2ccccc21
Reaction #1250281
title product
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(c1ccc(Oc2ccccc2)cc1)N1CCC(N2CCCC2)C1
Reaction #1263237
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(F)cc1)N1CC[C@H](N2CCCC2)C1
Reaction #1263246
(3′S)-1′-(4-fluorobenzoyl)-1,3′-bipyrrolidine
المردود 57.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي