Recherche de Sous-structure

C#CCCCCCCO

COC(=O)COCC#CC[C@@H]1[C@@H](c2ccc(C(O[Si](C)(C)C(C)(C)C)C3CCCCC3)cc2)[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1O
Reaction #9335
alcohol
Rendement 61.9%DOI: 10.6084/m9.figshare.5104873.v1
C#CCC1CCC(C(=O)OC)CC1
Reaction #44335
89
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1CCC(CC#Cc2nc(N)c3ncn(C4OC(C(=O)NCC)C(O)C4O)c3n2)CC1
Reaction #44341
JR3037
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1OC(n2cnc3c(N)nc(C#CCC4CCC(C(N)=O)CC4)nc32)C(O)C1O
Reaction #44342
JR3055
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1OC(n2cnc3c(N)nc(C#CCC4CCC(C(=O)NC)CC4)nc32)C(O)C1O
Reaction #44343
JR3065
Rendement 48.0%DOI: 10.6084/m9.figshare.5104873.v1
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
CC(C)(C)[Si](C)(C)OCC1CC1CCC#CCOC1CCCCO1
Reaction #65088
2-(5-tetrahydropyranyloxy-3-pentynyl)cyclopropylmethyl t-butyldimethylsilyl ether
Rendement 82.6%DOI: 10.6084/m9.figshare.5104873.v1
OCC1CC1CCC#CCOC1CCCCO1
Reaction #65089
2-(5-tetrahydropyranyloxy-3-pentynyl)cyclopropanemethanol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC1CCC#CC=O
Reaction #65090
compound
Rendement 97.1%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
CCC#CCC1(C(=O)OC)C(O)CCC1CC(=O)OC
Reaction #74827
compound ( 1-a )
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCC1(C(=O)OC(C)(C)C)C(O)CCC1CC(=O)OC
Reaction #74828
compound ( 1-a )
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC(C)(C)C)C(O)CCC1CC(=O)OC
Reaction #74831
compound ( 1-b )
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCC(CC#CCCCC(=O)O)S(C)(=O)=O
Reaction #93921
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCC(CC#CCCCC(=O)O)S(C)(=O)=O
Reaction #93922
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCCCCCC(OC)OC
Reaction #95554
1,1-dimethoxy-oct-7-yne
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(CCCCCC#CCCCCCC=O)OC
Reaction #95555
tetradec-7-yn-1,14-dial dimethylacetal
Rendement 84.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C#CCCCCCCBr)cc1Cl
Reaction #173410
DOI: 10.1039/C8SC04228D
C=CCCOC1C#CCCCCC1
Reaction #180846
DOI: 10.1039/C8SC04228D
C#CCCCCCCOC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #182741
DOI: 10.1039/C8SC04228D
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