Substructure Search

360827

CC(=O)[C@@H]1CC[C@@H](C)C[C@@H]1O
Reaction #160378
(1R,2S,4R)-1-(2-Hydroxy-4-methyl-cyclohexyl)-ethanone
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1CC(C)C2CC=C(C)C1C2
Reaction #229201
DOI: 10.1039/C8SC04228D
CC1CCC2C(C)C=COC2C1
Reaction #311727
4a,5,6,7,8,8a-hexahydro-4,7-dimethyl-4H-1-benzopyran
Yield 49219.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CC[C@@H](C2(C)CO2)[C@H](O)C1
Reaction #312596
isopulegol epoxide
Yield 160.4%DOI: 10.6084/m9.figshare.5104873.v1
COC1CC(C)C2CC=C(C)C1C2
Reaction #343278
title compound
Yield 71.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(C)OC
Reaction #343279
title compound
Yield 107.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CC(C)C2CC=C(C)C1C2
Reaction #343280
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CO[C@@H]2O[C@@]3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3
Reaction #358729
9,10-anhydro-10-deoxoartemisinin
Yield 36.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCCC(C)CC=Cc1ccc(C(C)C)cc1
Reaction #367246
desired product
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCCC(C)CC=Cc1ccc(C(C)C)cc1
Reaction #367250
desired product
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CO[C@@H]2O[C@@]3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3
Reaction #567393
9,10-anhydrodehydroartemisinin
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CO[C@@H]2O[C@@]3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3
Reaction #567395
9,10-anhydrodehydroartemisinin
Yield 172.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@@H](C)C[C@H]1O
Reaction #694522
Isopulegol
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@@H](C)C[C@H]1O
Reaction #694523
Isopulegol
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #694524
aluminium siloxide
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C2=C(Cl)C(=O)C=C(C)[C@]2(C)[C@H]2CC[C@]3(C)C(=O)[C@H](F)C[C@H]3[C@@H]2[C@@H]1C
Reaction #708812
16α-fluoro-4-chloro-1,7α-dimethyl-6-methylenandrosta-1,4-diene-3,17-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@@H]1CC[C@@H](C)C[C@H]1O
Reaction #742289
titled compound
Yield 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1CCC(C)CC1O
Reaction #785372
DOI: 10.1039/C8SC04228D
CC(=O)[C@@H]1CC[C@@H](C)C[C@@H]1O
Reaction #836553
(1R, 2S, 4R)-1-(2-Hydroxy-4-methyl-cyclohexyl)-ethanone
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@@H]1CC[C@@H](C)C[C@H]1O
Reaction #1093486
(1R, 2R, 5R)-2-Acetyl-5-methyl cyclohexanol
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1
Page 1Next