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CC(=O)OCCCCCCCCC=C

CC[C@H](C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(=O)O3)[C@H]21
Reaction #76282
lovastatin
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79374
compounds A
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)OC(C)(C)C)C(=O)OC(O)C(=O)[C@H]1[C@H](C)C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C
Reaction #81346
N-(N-(N-(N-((1,1-dimethyl) ethoxycarbonyl) -L-alanyl) -L-alanyl)-L-prolyl)-L-valine [6α-fluoro-11β,21-dihydroxy-16α-methyl-3,20-dioxo-pregna-1,4-dien-21-yl] ester
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81458
title compound
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1=CC2=CC[C@@H]3[C@H](CC[C@]4(C)C(c5cccnc5)=CC[C@@H]34)[C@@]2(C)CC1
Reaction #81466
title compound
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@@H]3[C@@H]2CC[C@]2(C)C(c4cccnc4)=CC[C@@H]32)C1
Reaction #81468
title compound
収率 84.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@@H]3[C@@H]2CC[C@]2(C)C(n4cnc5c(Cl)ncnc54)=C(C=O)C[C@@H]32)C1
Reaction #87331
21a
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)CO
Reaction #92982
above-identified compound
収率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)C(C)(C)C
Reaction #92998
above-identified compound
収率 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CCCC(=O)O
Reaction #92999
above-identified compound
収率 56.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CC1CCCC1
Reaction #93001
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C)C(=O)OCC(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #93002
above-identified compound
収率 19.8%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CC(C)=O
Reaction #93004
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CC(C)(C)C
Reaction #93011
above-identified compound
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)[C@H](CC(C)C)NC(=O)OC(C)(C)C
Reaction #93016
above-identified compound
収率 80.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)C1C(C)CC2C3CC(Cl)C4=CC(=O)C=CC4(C)C34OC4CC21C
Reaction #174878
DOI: 10.1039/C8SC04228D
CCC1CC2C3CCC4=CC(=O)CCC4C3CCC2(C)C1OC(=O)COC(=O)CC(C)(C)C
Reaction #181613
DOI: 10.1039/C8SC04228D
CC(=O)OC1CCC2(C)C(CCC3C2CC(OC(C)=O)C2(C)C(C(C)=O)CCC32)C1
Reaction #200002
DOI: 10.1039/C8SC04228D
CCC(C)(C)C(=O)OC1CC(C)C=C2C=CC(C)C(CCC3CC(O)CC(=O)O3)C21
Reaction #203193
DOI: 10.1039/C8SC04228D
CC1CC2C3CC(F)C4=CC(=O)CCC4(C)C3=CCC2(C)C1(O)C(=O)CO
Reaction #209760
DOI: 10.1039/C8SC04228D
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