Recherche de Sous-structure

302878

CCCCCC1(CC[C@@H]2[C@@H](CC(O)C(F)(F)C#CCCO[Si](C)(C)C(C)(C)C)[C@@H](O[SiH2]C(C)(C)C)C[C@H]2OC2CCCCO2)OCCO1
Reaction #50200
title compound ( 65 )
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
C#C[C@H]1C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12
Reaction #70374
title compound
Rendement 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC2=C(C#Cc3ccccc3)CCCC21
Reaction #71255
(±)-(RS)-4-phenylethynyl-2,3,5,6,7,7a-hexahydro-indole-1-carboxylic acid ethyl ester
Rendement 1.1%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
CCCCC[C@H](O)C#CCC(CCCCCCC(=O)O)S(C)(=O)=O
Reaction #93924
8-methylsulfonyl-12(S)-hydroxy-10-heptadecynoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(CC#CC1(O)CCCCC1)CCCCCCC(=O)O
Reaction #93928
8-methylsulfonyl-11-(1-hydroxycyclohexyl)-10-undecynoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(CCCCCCC(=O)O)CCCC1(O)CCCCC1
Reaction #93929
8-methylsulfonyl-11-(1-hydroxycyclohexyl)-undecanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C#CC1=CCC2C3CCC4=CC(=O)C=CC4(C)C3CCC12C
Reaction #176247
DOI: 10.1039/C8SC04228D
CCCCCCCCC#CCOC1CCCCO1
Reaction #180682
DOI: 10.1039/C8SC04228D
O=C1OC(CCC#Cc2cccc(O)c2)(C2CCCC2)CC(O)=C1Sc1nccs1
Reaction #211959
DOI: 10.1039/C8SC04228D
C#CC[C@@H](C(=O)OC)[C@H](O)C[C@@H](CCCCCCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C
Reaction #216251
methyl (2R,3R,5R)-5-(t-butyldimethylsiloxy)-3-hydroxy-2-(2-propynyl)docosanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC#CCO
Reaction #222327
DOI: 10.1039/C8SC04228D
C#CC(O)CC1CCCCC1
Reaction #233419
DOI: 10.1039/C8SC04228D
CC(=O)C1CCC2C3CCC4CC(O)(C#CCl)CCC4(C)C3CCC12C
Reaction #253835
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCC2=C(C#Cc3ccccc3)CCCC21
Reaction #280332
DOI: 10.1039/C8SC04228D
CCCCCCCCC#Cc1coc2ccc(CN(Cc3ccc(C(F)(F)F)cc3)C(=O)C(=O)OCC)cc12
Reaction #283293
DOI: 10.1039/C8SC04228D
C#CCC1CC2C(CCC3(C)C(=O)CCC23)C2(C)C=CC(=O)C=C12
Reaction #288679
DOI: 10.1039/C8SC04228D
Page 1Suivant