Busqueda de Subestructura

CCCC1CCC(=O)CC1

CCc1cc(N[C@H]2CC[C@@H](C(C)(C)CC(C)(C)C)CC2)c(Br)cn1
Reaction #1120
2-Ethyl-4-[cis-4-(1,1,3,3-tetramethylbutyl)cyclohexylamino]-5-bromopyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1nccc(N[C@H]2CC[C@@H](C(C)(C)CC(C)(C)C)CC2)c1OC
Reaction #1121
2,3-Dimethoxy-4-[cis-4-(1,1,3,3-tetramethylbutyl)cyclohexylamino]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[Si]1(c2ccccc2)CCC(C2CCC(C=O)CC2)CC1
Reaction #2754
4-(4-n-pentyl-4-phenyl-4-silacyclohexyl)cyclohexane carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
ON=C1C2CC3CC1CC(O)(C3)C2
Reaction #41094
5-hydroxy-adamantan-2-one oxime
Rendimiento 73.4%DOI: 10.6084/m9.figshare.5104873.v1
NC1C2CC3CC1CC(O)(C3)C2
Reaction #41096
4-amino-adamantan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(N)C2CC3CC1CC(O)(C3)C2
Reaction #66725
4-allyl-4-amino-adamantan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C12CC3CC(C1)C(=O)C(C3)C2
Reaction #66728
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H](SC3CCNC3)CC1/C(=N/O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12.O=C(O)/C=C/C(=O)O
Reaction #70354
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1CC(=O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70386
3β-hydroxyandrostane-7,17-dione
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1CC(=O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70387
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC2CC(=O)CC[C@]2(C)[C@H]2CC[C@]3(C)C(=O)CC[C@H]3[C@H]12
Reaction #70394
title compound
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)C(C1)C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70403
3β-tert-butyldimethylsilyloxyandrostane-6,17-dione
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70404
3β-hydroxyandrostane-6,17-dione
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1C2CC3CC1CC(O)(C3)C2
Reaction #159303
1,4-dihydroxyadamantane
DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccccc1C(=O)OCCCC1CCC(=O)CC1=O
Reaction #164454
6
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cc(NC(=O)OCCCC3CCC(=O)CC3=O)c(=O)oc2c1
Reaction #164455
7
Rendimiento 59.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CCC(=O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172730
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)OC(C)(C)C)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CCC(=O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172945
tert-butyl ((1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-3a-yl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1CCC2C3CCC4CC(O)C(C)CC4(C)C3C(=O)CC12C
Reaction #174790
DOI: 10.1039/C8SC04228D
N#CC1(C2CCOCC2)CCC(=O)CC1
Reaction #175867
DOI: 10.1039/C8SC04228D
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