Substructure Search

CCCCCCCCCCCCCCCCC(O)CO

CCCCCCCCCCCCCCCCC(O)COC1CCCCO1
Reaction #1219
1-(2-tetrahydropyranyloxy)-2-octadecanol
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[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 #70365
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](C=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70366
6α-Formylandrostane-3,17-dione
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](NC=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70372
title compound
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C(=C(F)F)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70373
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@H]1C[C@@H]2[C@H](CC[C@@]3(C)[C@H]2CC24OCCOC23OCCO4)[C@@]2(C)CCCCC12
Reaction #70375
17,17-Bis(ethylendioxy)-6α-vinylandrostane
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1[C@@H](CCO)C[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #70376
17,17-Bis(ethylendioxy)-6α-(2-hydroxyethyl)androstane
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](CCO)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70377
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C/C(=N\O)[C@@]4(O)CCCC[C@]34C)[C@@H]1CC13OCCOC12OCCO3
Reaction #70382
17,17-Bis(ethylendioxy)-5α-hydroxy-6-(E)-hydroxyimino-androstane
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC2CCCC[C@]2(C)[C@H]2CC[C@@]3(C)[C@@H](CC45OCCOC43OCCO5)[C@H]12
Reaction #70393
17,17-Bis(ethylendioxy)-7-methyleneandrostane
Yield 85.0%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
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1C[C@H](CO)[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #70395
17,17-bis(ethylendioxy)-7β-hydroxymethylandrostane
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C[C@@H](CO)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70396
7α-Hydroxymethylandrostane-3,17-dione
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C[C@H](CO)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70397
7β-Hydroxymethylandrostane-3,17-dione
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70398
title compound
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1C[C@@H](NC=O)[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #70399
17,17-Bis(ethylendioxy)-7α-formamidoandrostane
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C[C@@H](C=O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70400
7α-Formylandrostane-3,17-dione
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CC[C@@H](O)C(C)(C)O)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](OC5CCCOC5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #95326
(24R)-5,7-cholestadiene-3β,24,25-triol 3-tetrahydropyranyl ether
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CC[C@@H](O)C(C)(C)O)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #95327
(24R)-5,7-cholestadiene-3β,24,25-triol
Yield 67.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCOC1CC2(C)C(CCC3C4CCC(C(C)=O)C4(C)CC(=O)C32)CC1O
Reaction #198323
DOI: 10.1039/C8SC04228D
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