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CCC=CCCCCC

CCCCC[C@@H]1OC(=O)[C@@H]1CCCC
Reaction #41999
3-butyl-4-pentyl-oxetan-2-one
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C1CCCCCC=C1Br
Reaction #74254
17
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)C1C#CCCCCC1
Reaction #74255
cyclooct-1-yn-3-glycolic acid
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@]23c4c5ccc(OCCCONC(=O)c6ccc(N=C=S)cc6)c4OC2C(O)C=C[C@H]3[C@H]1C5
Reaction #81574
N-[3-[(7,8-Didehydro-4,5-epoxy-6-hydroxy-17-methylmorphinan-3-yl)oxy]propoxy]-4-isothiocyanatobenzamide
Выход 40.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCC1=CCCC1=O
Reaction #95250
2-(5-carbethoxypentyl)-2-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)CN3C(=O)OC[C@@H]3c3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172774
title compound
Выход 30.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCS(=O)(=O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O[C@H]7O[C@H](C(=O)OCc8ccccc8)[C@@H](O)[C@H](O)[C@H]7O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172892
desired product
Выход 14.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCS(=O)(=O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O[C@H]7O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]7O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172893
desired product
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCN(C(=O)OC(C)(C)C)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172904
desired product
Выход 52.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCN(C(=O)OC(C)(C)C)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172905
desired product
Выход 40.8%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCNCC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12.Cl
Reaction #172917
desired product
Выход 87.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C(=O)[C@@]2(C)[C@H]([C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)c4ccccc4)c4ccccc4)C(C)=C1C3(C)C)[C@]1(OC(C)=O)CO[C@@H]1C[C@@H]2O
Reaction #218931
paclitaxel
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C1CCCCCC=C1Br
Reaction #266216
DOI: 10.1039/C8SC04228D
CN1CCC23c4c5ccc(OCCCONC(=O)c6ccc(N=C=S)cc6)c4OC2C(O)C=CC3C1C5
Reaction #292297
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2C3CC=C4CC(NCCCNC(=O)CCNC(=O)CCNC(=O)CCCCCNc5ccc([N+](=O)[O-])cc5[N+](=O)[O-])CCC4(C)C3CCC12C
Reaction #296330
DOI: 10.1039/C8SC04228D
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](NCCCNC(=O)CCNC(=O)CCNC(=O)CCCCCNc5ccc([N+](=O)[O-])cc5[N+](=O)[O-])CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #306483
2
Выход 73.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](NCCCNC(=O)CCNC(=O)CCCCCNc5ccc([N+](=O)[O-])cc5[N+](=O)[O-])CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #306484
3
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCC1=C(Br)CCC1=O
Reaction #319107
7-(2-bromo-5-oxo-1-cyclopentenyl) heptanoic acid
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C(=O)[C@@]2(C)[C@H]([C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)c4ccccc4)c4ccccc4)C(C)=C1C3(C)C)[C@]1(OC(C)=O)CO[C@@H]1C[C@@H]2O.CC(C)(NCC(O)COc1cccc2[nH]c3ccccc3c12)c1ccc(N=[N+]=[N-])cc1.CC(C)C[C@H](N)C(=O)O
Reaction #324598
9
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C(=O)[C@@]2(C)[C@H]([C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)c4ccccc4)c4ccccc4)C(C)=C1C3(C)C)[C@]1(OC(C)=O)CO[C@@H]1C[C@@H]2O.CC(C)(NCC(O)COc1cccc2[nH]c3ccccc3c12)c1ccc(N=[N+]=[N-])cc1.CC(C)C[C@H](NC(=O)[C@@H](N)CO)C(=O)O
Reaction #324599
12
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
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