Recherche de Sous-structure

CCC#CCO

C[C@H](C#CC(=O)c1ccc(NC(=O)c2cnccn2)cc1F)O[Si](C)(C)C(C)(C)C
Reaction #41699
compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CCC(=O)c1ccc(NC(=O)c2cnccn2)cc1F)O[Si](C)(C)C(C)(C)C
Reaction #41700
compound
DOI: 10.6084/m9.figshare.5104873.v1
OC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50176
4-hydroxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
Rendement 88.3%DOI: 10.6084/m9.figshare.5104873.v1
COC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50177
4-methoxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
Rendement 96.1%DOI: 10.6084/m9.figshare.5104873.v1
COC1(C#CCO)CCOCC1
Reaction #50178
4-methoxy-4-(3-hydroxyprop-1-ynyl)tetrahydropyran
Rendement 47.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOCO[C@H]1CC[C@@]2(C)[C@H](CC[C@@H]3[C@@H]2CC[C@]2(C)C(O)(CCC(=O)O)CC[C@]32O)C1
Reaction #50277
17-hydroxy-17-(2-carboxyethyl)-3beta-ethoxymethoxy-14-hydroxy-5beta,14beta-androstane
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](C#CCOS(C)(=O)=O)CC1
Reaction #53911
trans-Methanesulfonic acid 3-{4-[(4-chloro-phenoxycarbonyl)-methyl-amino]-cyclohexyl}-prop-2-ynyl ester
Rendement 117.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Nc1ccc(Cl)cc1)[C@H]1CC[C@H](C#CCOS(C)(=O)=O)CC1
Reaction #53912
trans-Methanesulfonic acid 3-{4-[3-(4-chloro-phenyl)-1-methyl-ureido]-cyclohexyl}-prop-2-ynyl ester
Rendement 101.9%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2
Reaction #57291
8
Rendement 96.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(O)cc2C(C#CC2CC2)(C(F)(F)F)O1
Reaction #57292
9
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2
Reaction #57294
11
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2)ON1C(=O)CCC1=O
Reaction #57295
12
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCC#CC(O)C1C(=O)C=CC1C=CC(O)C1CCCC1
Reaction #63768
4-(3-hydroxy-3-cyclopentyl-1-propenyl)-5-(1-hydroxy-6-methoxycarbonyl-2-hexyn-yl)-2-cyclopentenone
Rendement 79.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)C#CCOC1CCCCO1
Reaction #81000
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)C#CCOC1CCCCO1
Reaction #82219
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC#CC(O)CCI
Reaction #95271
product
DOI: 10.6084/m9.figshare.5104873.v1
CCCC#CC(CCI)OC(C)(C)C
Reaction #95272
3-t-butoxy-1-iodo-4-octyne
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CO[C@@H](C)CC#CCOC1CCCCO1)OCC
Reaction #155620
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCOCC#CCc1cn([C@H]2CC[C@@H](CO)O2)c(=O)[nH]c1=O)C(F)(F)F
Reaction #164142
product 5
Rendement 43.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCOCC#CCc1cn([C@H]2CC[C@@H](COP(=O)(O)O)O2)c(=O)[nH]c1=O)C(F)(F)F
Reaction #164143
mono phosphate
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant