Busqueda de Subestructura

12492

C#CCN1CCCCC1
Reaction #6885
1-(2-propynyl)piperidine
DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(C)Nc1ccc(Br)cc1
Reaction #48313
product
DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cccnc1Cl
Reaction #55315
2-chloro-3-(2-propynyloxy)pyridine
Rendimiento 52.2%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOCc1cccnc1
Reaction #55318
3-(2-propynyloxymethyl)pyridine
Rendimiento 45.3%DOI: 10.6084/m9.figshare.5104873.v1
CC#COc1ccncc1
Reaction #55319
4-(propynyloxy)pyridine
Rendimiento 3.6%DOI: 10.6084/m9.figshare.5104873.v1
C#CCSc1ccncc1
Reaction #55320
4-(2-propynylthio)pyridine
Rendimiento 40.2%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)C(CC(=O)OCC#CCCl)c1ccccc1
Reaction #56105
title compound
Rendimiento 25.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #62732
needles
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cc(C(=O)OC)cc(OC)c1OC
Reaction #62738
methyl 3,4-dimethoxy-5-(2-propynyloxy)benzoate
Rendimiento 49.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1I
Reaction #66666
5-(5-iodo-2-isopropyl-4-prop-2-ynyloxy-phenoxy)-pyrimidine-2,4-diamine
Rendimiento 71.8%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(C)N1CCC(O)CC1
Reaction #75596
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(C)N1CCN(c2cc3c(cc2C(C)=O)C(=O)c2c([nH]c4cc(C#N)ccc24)C3(C)C)CC1
Reaction #90074
title compound
Rendimiento 35.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1ccc(-n2cnnn2)nc1
Reaction #167822
5-(Prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cccnc1C
Reaction #167843
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1I
Reaction #168986
5-(5-iodo-2-isopropyl-4-prop-2-ynyloxy-phenoxy)-pyrimidine-2,4-diamine
Rendimiento 71.8%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCC(NS(=O)(=O)c2ccc(OCc3cc(C)nc4ccccc34)cc2)C(C)(C(=O)NOC(C)(C)C)C1
Reaction #178435
DOI: 10.1039/C8SC04228D
C#CC(=O)OC1CCN(C)C(=O)N1c1nnc(C(C)(C)C)s1
Reaction #191414
DOI: 10.1039/C8SC04228D
C#CC(C)(C)N(CC)CCO
Reaction #194299
DOI: 10.1039/C8SC04228D
Nc1ccnc(SCC#CCN2C(=O)c3ccccc3C2=O)n1
Reaction #195568
DOI: 10.1039/C8SC04228D
C=C(F)C(Cl)C#CC(C)(C)C
Reaction #197800
DOI: 10.1039/C8SC04228D
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