Substructure Search

678246

O=C(C#CCCO)OCc1ccccc1
Reaction #288475
DOI: 10.1039/C8SC04228D
CCOC(=O)C#CC(C)(C)CO[Si](C)(C)C
Reaction #325026
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C#CCCOC1CCCCO1
Reaction #325029
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C#CCCO
Reaction #325030
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(CCO)n2c(n1)O[C@H](COc1ccc(C3CCCCC3)cc1)C2
Reaction #325031
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C)OCCC#CC(=O)OCc1ccccc1
Reaction #1212318
DOI: 10.1039/C8SC04228D
C#CC[C@H](O)[C@H](O)[C@@H](N)CC1CCCCC1
Reaction #1338796
amine
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C#CCC(O)C(O)C(N)CC1CCCCC1
Reaction #1676046
(tert-butyloxycarbonyl]-6-(amino)-4,5-dihydroxy-7-cyclohexyl-1-heptyne
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C#CCC(O)C(O)C(N)CC1CCCCC1
Reaction #1816244
(tert-butyloxylcarbonyl]-6-(amino)-4,5-dihydroxy-7-cyclohexyl-1-heptyne
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC[C@H](O)[C@H](O)[C@@H](N)CC1CCCCC1
Reaction #1816245
amine
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C)OCCC#CC(=O)OCc1ccccc1
Reaction #1924263
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C#CCCO)OCc1ccccc1
Reaction #1924264
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(OCc2ccccc2)CCO1
Reaction #1924265
title compound
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C#CCCO)OCc1ccccc1
Reaction #1949617
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1