Recherche de Sous-structure

1328303

OCCCCCCCCI
Reaction #49713
8-iodooctan-1-ol
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Rendement 84.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cnc(Cl)cc2C)C(=O)C2C3CCC(O3)C12
Reaction #69963
4-(6-chloro-4-methyl-pyridin-3-yl)-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Rendement 64.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)C(CCCCCCCCOc1ccc(OC)cc1Cl)C(C)=O
Reaction #178702
DOI: 10.1039/C8SC04228D
CC(=O)OC1CCC2C3CCC4=CC(=O)C=C(C)C4(C)C3CCC12C
Reaction #179421
DOI: 10.1039/C8SC04228D
ICCCC1OCCOC1CC1COCCO1
Reaction #191637
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCCCCCI)(CCCC(F)(F)C(F)(F)F)C(=O)OCC
Reaction #261598
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2C3CC(Br)=C4CC(O)CCC4(C)C3CCC12C
Reaction #294948
DOI: 10.1039/C8SC04228D
COC(=O)CCCC(I)C1C[C@@H]2[C@@H](/C=C/[C@@H](O)C(C)CCCCCl)[C@H](O)C[C@@H]2O1
Reaction #311508
title compound
Rendement 74.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C1/C[C@@H]2[C@@H](/C=C/[C@@H](O)C(C)CCCCCl)[C@H](O)C[C@@H]2O1
Reaction #311509
title compound
Rendement 58.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCCCCI
Reaction #314516
t-butyl-8-iodooctanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)C(I)[C@H](C)[C@]4(C)[C@H]3CC[C@]12C
Reaction #362252
17β-acetoxy-2-iodo-1α-methyl-androst-4-en-3-one
Rendement 93.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)C=C(C)[C@]4(C)[C@H]3CC[C@]12C
Reaction #362253
17β-Acetoxy-1-methyl-androsta-1,4-dien-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)C(I)C[C@]4(C)[C@H]3CC[C@]12C
Reaction #362254
crude product
Rendement 98.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CCC2C3CCC4=CC(=O)C=CC4(C)C3CCC12C
Reaction #396850
DOI: 10.1039/C8SC04228D
C[C@H](C[C@@H]1C=CC(=O)C1)[C@H]1CCC2C(O[Si](C)(C)C)CCC[C@@]21C
Reaction #654587
(4S)-4-{(2R)-2-[(1R,7aR)-octahydro-4-trimethylsilyloxy-7a-methyl-1H-inden-1-yl]-propyl}-2-cyclopenten-1-one
Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](CCCCI)C[C@H](NC(=O)OC(C)(C)C)C(=O)OC
Reaction #713008
crude product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](C[C@@H]1C=CC(=O)C1)[C@H]1CCC2C(O[Si](C)(C)C)CCC[C@@]21C
Reaction #950516
(4S)-4-{(2R)-2-[(1R,7aR)-octahydro-4-trimethylsilyloxy-7a-methyl-1H-inden-1-yl]-propyl}-2-cyclopenten-1-one
Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC[C@@H](C)[C@H]1CCC[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)CCC[C@]12C
Reaction #1162737
(R)-5-[(1R,4aR,5S,8aR)-5-(tert-Butyl-dimethyl-silanyloxy)-8a-methyl-decahydro-naphtalen-1-yl)-hexanoic acid ethyl ester
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCCSCCCCCCCC(=O)OCC
Reaction #1178129
ethyl 9-thia-12-oxatetradecanoate
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
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