بحث البنية الفرعية

C#CCC

CCCCC#CC#CCOc1ccc(C(=O)OCC)cc1
Reaction #2735
ethyl 4-(2,4-nonadiynyloxy)-benzoate
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCCC(=O)N1c2ccccc2C(=O)Nc2cccnc21
Reaction #4263
5,11-Dihydro-11-[1-oxo-4-pentynyl]-6H-pyrido[2,3-b][1,4]-benzodiazepin-6-on
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cccnc2N(C(=O)CCC#CCN2CCCCC2)c2ccccc21
Reaction #4270
5,11-Dihydro-11-[1-oxo-6-(1-piperidinyl)-4-hexynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(CC#CCN1CCN(C)CC1)C(=O)N1c2ccccc2C(=O)Nc2cccnc21
Reaction #4271
5,11-Dihydro-11-[1-oxo-2-methyl-6-(4-methyl-1-piperazinyl)-4-hexynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(CC#CCN1CCN(C)CC1)C(=O)N1c2ccccc2C(=O)Nc2cccnc21.Cl.Cl
Reaction #4272
5,11-Dihydro-11-[1-oxo-2-methyl-6-(4-methyl-1-piperazinyl)-4-hexynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC#CC1(O)C(=O)Nc2ccc(Br)cc21
Reaction #7087
5-bromo-3-hydroxy-3-prop-1-ynyl-1,3-dihydroindol-2-one
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CCC#CC(O)CC2=C(C)CCC2=O)c1
Reaction #55935
3-methyl-2-[6-(m-methoxyphenyl)-2-hydroxy-3-hexynyl]-2-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CC/C=C/C(CC2=C(C)CCC23SCCS3)OCc2ccccc2)c1
Reaction #55936
product
DOI: 10.6084/m9.figshare.5104873.v1
C#CC12CC3CC(C#C)(C1)CC(C14CC5CC(C#C)(CC(C#C)(C5)C1)C4)(C3)C2
Reaction #67394
3,3′,5,5′-tetraethynyl-1,1′-biadamantane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCc2cc(C#CCCCO)ccc21
Reaction #77767
6-(5-Hydroxy-pent-1-ynyl)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester
المردود 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCc2cc(CCCCCO)ccc21
Reaction #77768
6-(5-Hydroxy-pentyl)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester
المردود 68.0%DOI: 10.6084/m9.figshare.5104873.v1
C#C[C@]1(O)C(=C)C[C@H]2[C@@H]3CC(=C)C4=CC(=O)CC[C@]4(C)[C@H]3CC[C@@]21C
Reaction #93683
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C[C@@H]2[C@H](CC[C@@]3(C)[C@H]2CC(=C)[C@@]3(O)C(C)=O)[C@@]2(C)CCC(=O)C=C12
Reaction #93684
17α-Acetyl-17β-hydroxy-6,16-dimethyleneandrosta-4-en-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(F)(CCC#C[Si](C)(C)C)C(C)=O
Reaction #95463
2-acetyl-2-fluoro-6-(trimethylsilyl)-5-hexynoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C#CCCCCl)ccc1-c1cnc(C)o1
Reaction #158392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(N)CCCC#Cc1ccc(-c2cnc(C)o2)c(OC)c1
Reaction #158393
title compound
المردود 58.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCc2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnn21
Reaction #158394
title compound
المردود 95.7%DOI: 10.6084/m9.figshare.5104873.v1
C#CC1=CCC2C3CCC4=CC(=O)C=CC4(C)C3CCC12C
Reaction #176247
DOI: 10.1039/C8SC04228D
CC#CC(O)(c1ccc(Cl)cc1Cl)C(C)n1cncn1
Reaction #181526
DOI: 10.1039/C8SC04228D
C#CCCCCC12OCC(CCC)(CS1)CS2
Reaction #183815
DOI: 10.1039/C8SC04228D
الصفحة 1التالي