Busqueda de Subestructura

730313

CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCC(=O)Cl)[C@@]4(C)CC[C@@H]32)C1
Reaction #3185
3β-acetoxy-5-cholenic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](O)C(=O)[C@@H]2[C@@]3(C)C[C@@H](c4ccoc4)OC(=O)[C@H]3CC[C@]21C
Reaction #40591
8a
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)C(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40592
10
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40598
34
Rendimiento 81.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)C(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40604
10
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](OC(=O)C(F)(F)F)C[C@@]21C
Reaction #48895
1-4
Rendimiento 94.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@H](CC[C@]4(C)C(=O)[C@@H](N5CCCCC5)C[C@@H]34)[C@@]2(C)C[C@@H]1N1CCCCC1
Reaction #65119
(2β,3α,5α,16β)-3-acetyloxy-2,16-di-(1-piperidinyl)androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)C(O)CO
Reaction #70102
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2,3-dihydroxypropanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OC(=O)CCC(=O)[O-])C1.[Na+]
Reaction #72433
sodium monomenthyl succinate
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OC(=O)CCC(=O)[O-])C1.[Na+]
Reaction #72434
sodium monomenthyl succinate
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OC(C)=O)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #83376
12-[2-(4-acetoxy-3-methoxycyclohexyl)-1-methylvinyl]-17-allyl-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@H]4[C@@H]3C[C@@H](NCCc3c[nH]cn3)[C@@]2(O)C1
Reaction #92671
5α-Hydroxy-6β-[2-(1H-imidazol-4-yl)-ethylamino]-cholestan-3β-yl butyrate
Rendimiento 60.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3[C@H](Cl)[C@H]3O[C@]32C1
Reaction #93689
7α-chloro-5,6β-epoxy-15β,16β-methylene-3β-pivaloyloxy-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3C=C[C@]2(O)C1
Reaction #93690
5-hydroxy-15β,16β-methylene-3β-pivaloyloxy-5β-androst-6-en-17-one
Rendimiento 74.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1C(C)CC(c2ccncc2N)CC1NC(=O)OC(C)(C)C
Reaction #160768
(+/−)-4-(3-aminopyridin-4-yl)-2-(tert-butoxycarbonylamino)-6-methylcyclohexyl acetate
Rendimiento 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCCO)c(F)c(C(Nc2ccc(C(N)=NC(=O)OCC(C)(C)C)cc2)c2nc(OCOC(=O)C(C)(C)C(=O)OC3CCCCC3)n(-c3ncccn3)n2)c1
Reaction #180183
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2(C#N)C3C=CC4C(C)(C)C(OC(=O)c5ccccc5)CCC4(C)C3CCC12C
Reaction #183662
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #187241
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2=CC=C3C4CCC(C(C)C5OCC(C)(C)CO5)C4(C)CCC3C2(C)C2OC12
Reaction #201225
DOI: 10.1039/C8SC04228D
CC(C)(C)C1CCC(OC(=O)C(=O)Cl)CC1
Reaction #202241
DOI: 10.1039/C8SC04228D
Página 1Siguiente