部分構造検索

C=C(C)CCCCCCCCC

CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #6396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CC1OC
Reaction #6400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81464
title compound
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #83380
17-allyl-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-12-[2-(4-methylthiomethoxy-3-methoxycyclohexyl)-1-methylvinyl]-11,28-dioxa-4-azatricyclo[22.2.1.04,9 ]octacosa-14,18-diene-2,3,10,16-tetraone
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)c1ccccc1
Reaction #93000
above-identified compound
収率 89.1%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(OC)C(=O)C(CCCCCCCCCCCO)=C(C)C1=O
Reaction #182352
DOI: 10.1039/C8SC04228D
CC(CCN1CCN(C)CC1)C1CC=C2C3=C(CCC21C)C1(C)CCC(O)C(C)(C)C1CC3
Reaction #183086
DOI: 10.1039/C8SC04228D
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1N=[N+]=[N-]
Reaction #185119
DOI: 10.1039/C8SC04228D
COC(=O)C1(OC(=O)c2ccc(O)o2)C(C)CC2C3CC(F)C4=CC(=O)C=CC4(C)C34OC4CC21C
Reaction #185648
DOI: 10.1039/C8SC04228D
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1NC(=O)C1CC1
Reaction #190231
DOI: 10.1039/C8SC04228D
CC(CC(O[SiH](C)C)C(=O)O)C1CC=C2C3=C(CCC21C)C1(C)CCC(C(C)(C)C)C(C)(C)C1CC3
Reaction #197427
DOI: 10.1039/C8SC04228D
CC1CC2C3CC(F)C4=CC(=O)C=CC4(C)C3C(O)CC2(C)C1C(=O)C(=O)O
Reaction #199931
DOI: 10.1039/C8SC04228D
CCCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1O
Reaction #202925
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(Oc4ccccc4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #203572
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(N=[N+]=[N-])C(OC)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #204864
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2=CC=C3C4CCC(C(C)C5OCC(C)(C)CO5)C4(C)CCC3C2(C)C2OC12
Reaction #208184
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OCC=Cc4ccccc4)C(OC)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #210866
DOI: 10.1039/C8SC04228D
CC(=O)OCC(=O)[C@@]1(OC(C)=O)CC[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)CC[C@]4(C)[C@@]34O[C@H]4C[C@@]21C
Reaction #214352
9β,11β-epoxy-6α-fluoro-17α,21-diacetoxy-4-pregnen-3,20-dione
収率 96.2%DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #223881
DOI: 10.1039/C8SC04228D
COC1=C(OC)C(=O)C(CCCCCCCCCCOC(C)=O)=C(C)C1=O
Reaction #235150
DOI: 10.1039/C8SC04228D
1 ページ次のページ