بحث البنية الفرعية

762968

Cc1ncccc1CCl
Reaction #1776
3-chloromethyl-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CCl)ccc[n+]1[O-]
Reaction #1777
3-Chloromethyl-2-methylpyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ncccc1CCl
Reaction #1782
2-ethyl-3-chloromethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(CCl)ccc[n+]1[O-]
Reaction #1783
2-ethyl-3-chloromethylpyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ncccc1CCl
Reaction #1785
2-isopropyl-3-chloromethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(CCl)ccc[n+]1[O-]
Reaction #1786
2-isopropyl-3-chloromethylpyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc(C)c1CCl
Reaction #1788
2,4-dimethyl-3-chloromethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc[n+]([O-])c(C)c1CCl
Reaction #1789
2,4-dimethyl-3-chloromethylpyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #5107
nicotinate ester
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(COc2ccc(Oc3ccccc3)cc2Cl)cn1
Reaction #5300
2-chloro-5-(2-chloro-4-phenoxyphenoxy)methylpyridine
المردود 70.8%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cccc(Oc2ccc(OCc3ccc(Cl)nc3)c(Cl)c2)c1
Reaction #5301
2-chloro-5-[2-chloro-4-(3-trifluoromethylphenoxy)phenoxy]methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(COc2ccc(Oc3cccc(Br)c3)cc2Cl)cn1
Reaction #5302
2-chloro-5-[4-(3-bromophenoxy)-2-chlorophenoxy]methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(CSCc2cccnc2)NC(C)=C(C#N)C1c1cccc([N+](=O)[O-])c1
Reaction #5744
(-)-2-(3-pyridinylmethylthio)methyl-5-cyano-3-carboethoxy-4-(3-nitrophenyl)-6-methyl-1,4-dihydropyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1ccc(OC(=O)c2cccnc2)c(OC(=O)c2cccnc2)c1)OCc1ccccc1
Reaction #6002
desired compound
المردود 71.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccnc1)c1ccc2c(c1)[Se](=O)C=N2
Reaction #6012
6-Nicotinoylbenzoselenazolinone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCSc1ccncc1)c1cccnc1
Reaction #6210
desired compound
المردود 75.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCOc1ccncc1)c1cccnc1
Reaction #6238
desired compound
المردود 88.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4cccnc4)c3C2=O)C(=O)N1
Reaction #10057
N-[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]-3-pyridylcarboxamide
المردود 79.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(CNC(=O)c4cccnc4)c3C2=O)C(=O)N1
Reaction #10061
[(2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}-3-pyridylcarboxamide
المردود 64.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc2[nH]c3c(NC(=O)c4cccnc4)cc(Cl)cc3c12
Reaction #40501
N-(6-chloro-4-methyl-9H-β-carbolin-8-yl)-nicotinamide
المردود 8.1%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي