Substructure Search

40865

C[C@@H]1OC(=O)[C@H](C)OC1=O.O=C1CCCCCO1
Reaction #2353
ε-CAPROLACTONE L-LACTIDE
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1OC(=O)[C@H](C)OC1=O.O=C1CCCCCO1
Reaction #2354
ε-CAPROLACTONE L-LACTIDE
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1OC(=O)[C@H](C)OC1=O.O=C1CCCCCO1
Reaction #2355
ε-CAPROLACTONE L-LACTIDE
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)Cc1ccc(C(=O)O)s1
Reaction #42387
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1c2cc(C(=O)O)ccc2CCN1C(=O)OC(C)(C)C
Reaction #42547
2-(tert-butoxycarbonyl)-1-butyl-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid
Yield 61.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #55561
methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC[C@H]1C(=O)CC[C@@H]1C=CC(O)C(C)(C)CC=C(C)C
Reaction #55562
residue
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC[C@H]1C(=O)CC[C@@H]1CCC(O)C(C)(C)CC=C(C)C
Reaction #55565
9-Keto-15-hydroxy-16,16,19-trimethyl-prost-18-enoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #70362
solid
Yield 75.0%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(=N/O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70370
title compound
Yield 70.0%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
CO/N=C1\C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12
Reaction #70378
title compound
Yield 70.0%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[C@]12CC[C@H]3[C@@H](C/C(=N\O)[C@@]4(O)CC(=O)CC[C@]34C)[C@@H]1CCC2=O
Reaction #70383
title compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
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