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946084

COC1CCCC(OCc2ccccc2)C1O[Si](C)(C)C(C)(C)C
Reaction #162168
racemic [1-benzyloxy-3-methoxy-2-cyclohexanoxy]tert-butyl-dimethylsilane
DOI: 10.6084/m9.figshare.5104873.v1
COC1CCCC(O)C1O[Si](C)(C)C(C)(C)C
Reaction #162169
racemic [1-Hydroxy-3-methoxy-2-cyclohexanoxy]tert-butyl-dimethylsilane
DOI: 10.6084/m9.figshare.5104873.v1
OC(c1ccc(C2CC2)cc1)c1ccncc1OC1CC(COCc2ccccc2)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #205659
DOI: 10.1039/C8SC04228D
CCc1ccc(Cn2cc(C3CC(COCc4ccccc4)C(OCc4ccccc4)C(OCc4ccccc4)C3OCc3ccccc3)c3ccccc32)cc1
Reaction #227992
DOI: 10.1039/C8SC04228D
CCCC1(O)C(O)C(OCc2ccccc2)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #359283
21
収率 79.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC12OC(C)(C)OC1C(OCc1ccccc1)C(OCc1ccccc1)C(OCc1ccccc1)C2OCc1ccccc1
Reaction #359284
22
収率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCOC1C(OCc2ccccc2)C(OCc2ccccc2)C(OCc2ccccc2)C(OCc2ccccc2)C1(CCC)OC(=O)CCC
Reaction #359285
26
収率 123.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(Cc2cc(C3CC(COCc4ccccc4)C(OCc4ccccc4)C(OCc4ccccc4)C3OCc3ccccc3)ccc2OC)cc1
Reaction #403453
DOI: 10.1039/C8SC04228D
CCN1C[C@@]2(COC)C3[C@@H](OC)C4C1[C@@]3(C1C[C@@]3(O)[C@H](OC(=O)c5ccc(OC)cc5)C1[C@]4(O)[C@@H](O)[C@@H]3OC)[C@@H](OC)C[C@H]2O
Reaction #526751
14-anisoylaconine
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@]12CN(C)[C@@H]3[C@@H]4[C@H](OC)[C@H]1[C@@]3([C@@H](OC)C[C@H]2O)[C@@H]1C[C@@]2(O)[C@H](O)[C@@H]1[C@]4(O)[C@@H](O)[C@@H]2OC
Reaction #526752
mesaconine
収率 55.8%DOI: 10.6084/m9.figshare.5104873.v1
COC1CCCC(OCc2ccccc2)C1O[Si](C)(C)C(C)(C)C
Reaction #614196
racemic [1-benzyloxy-3-methoxy-2-cyclohexanoxy]tert-butyl-dimethylsilane
DOI: 10.6084/m9.figshare.5104873.v1
COC1CCCC(O)C1O[Si](C)(C)C(C)(C)C
Reaction #614197
racemic [1-Hydroxy-3-methoxy-2-cyclohexanoxy]tert-butyl-dimethylsilane
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cc2cccc(C3(O)C[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)c2)cc1
Reaction #641667
title compound
収率 29.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cc2cccc(C3(OC(C)=O)C[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)c2)cc1
Reaction #641668
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cc2cccc([C@@H]3C[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c2)cc1
Reaction #641669
title compound
収率 87.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(C2CC2)cc1)c1ccncc1O[C@@H]1C[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #641735
title product
収率 71.1%DOI: 10.6084/m9.figshare.5104873.v1
OC(c1ccc(C2CC2)cc1)c1ccncc1O[C@@H]1C[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #641736
title product
収率 101.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(COC[C@H]2C[C@@H](Oc3cnccc3Cc3ccc(C4CC4)cc3)[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)cc1
Reaction #641737
title product
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(O[C@@H]2C[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)c(Cc2ccc(C3CC3)cc2)s1
Reaction #641742
title compound
収率 58.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(Cc2cc([C@@H]3C[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2OC)cc1
Reaction #641750
title compound
収率 8.4%DOI: 10.6084/m9.figshare.5104873.v1
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