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C1C(CO1)O

COc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)cc1O
Reaction #8837
combretastatin A-4
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccccc1C(=O)OC1COC1
Reaction #64294
2-(Oxetan-3-oxycarbonyl)phenylsulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@]12CO[C@@H]1C[C@H](O)[C@@]1(C)C(=O)[C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)c4ccccc4)C[C@@](O)([C@@H](OC(=O)c4ccccc4)[C@H]21)C3(C)C.OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #72406
Docetaxel Mannitol
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@]12CO[C@@H]1C[C@H](O)[C@@]1(C)C(=O)[C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)c4ccccc4)C[C@@](O)([C@@H](OC(=O)c4ccccc4)[C@H]21)C3(C)C.OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #72407
Docetaxel Mannitol
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 #81357
Taxol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1O[C@H](CO)[C@@H]1O
Reaction #83112
desired product
Ausbeute 96.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(OC3COC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #89990
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC2COC2)c(C)c1
Reaction #160130
methyl 3-methyl-4-(oxetan-3-yloxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)O)ccc1OC1COC1
Reaction #160131
3-methyl-4-(oxetan-3-yloxy)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C2(O)COC2)cc1
Reaction #160159
4-(3-Hydroxyoxetan-3-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(-n3ncc(C(=O)c4cc5ccc(OC6COC6)cc5[nH]4)c3N)ccc2[nH]1
Reaction #161634
[5-amino-1-(2-methyl-1H-benzimidazol-5-yl)-1H-pyrazol-4-yl]-[6-(oxetan-3-yloxy)-1H-indol-2-yl]-methanone
Ausbeute 29.0%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
Reaction #218931
paclitaxel
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Br)cc1Cc1ccc(OC2COC2)cc1
Reaction #239118
DOI: 10.1039/C8SC04228D
CC(CO)(CC(Cc1ccc(-c2ccccc2)cc1)NC(=O)c1cnn[nH]1)C(=O)OC1COC1
Reaction #254776
DOI: 10.1039/C8SC04228D
Clc1nccc(OC2COC2)n1
Reaction #262389
DOI: 10.1039/C8SC04228D
O=C1N(c2ccc(C3(O)COC3)cc2)CCC12CCN(S(=O)(=O)c1ccccc1Cl)CC2
Reaction #267268
DOI: 10.1039/C8SC04228D
O=Cc1ccccc1
Reaction #321430
benzaldehyde
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)OCC1c2ccccc2-c2ccccc21)C(=O)O
Reaction #324597
8
Ausbeute 93.0%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
Ausbeute 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
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
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