Substructure Search

COC(C)(C)CCO

COc1ccc(C(OC[C@@]2(COS(=O)(=O)c3ccc(C)cc3)O[C@@H](n3cc(C)c(=O)[nH]c3=O)[C@H](O)[C@H]2OCc2ccccc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #6875
nucleoside
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccccc1C1(OCCCOC2(c3ccccc3C#C)C=CN3C(=O)c4cc(OC)ccc4N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]32)C=CN2C(=O)c3cc(OC)ccc3N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]21
Reaction #47142
17
Yield 92.7%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccccc1C1(OCCCOC2(c3ccccc3C#C)C=CN3C(=O)c4cc(OC)ccc4N=C[C@H]32)C=CN2C(=O)c3cc(OC)ccc3N=C[C@H]21
Reaction #47143
glass
Yield 38.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1OCc1ccccc1)CCC(C)(CCO)O2.Cc1ccc(S(=O)(=O)O)cc1
Reaction #55063
rac.-6-Benzyloxy-2,5,7,8-tetramethylchroman-2-ethanol p-toluenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(C#N)c2cc3nonc3cc2O1
Reaction #64364
8-cyano-6,6-dimethyl-6H-pyrano[2,3-f]benzo-2,1,3-oxadiazole
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
CCOc1ccc(Cc2cc([C@]34OC[C@](COC(C)=O)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87470
product
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCOc1ccc(Cc2cc([C@]34OC[C@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87472
Acetic acid 2-{4-[2-chloro-5-((1S,2S,3S,4R,5S)-2,3,4-trihydroxy-1-hydroxymethyl-6,8-dioxa-bicyclo[3.2.1]oct-5-yl)-benzyl]-phenoxy}-ethyl ester
Yield 22.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCOc1ccc(Cc2cc([C@]34OC[C@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87473
desired compound
Yield 26.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCOc1ccc(Cc2cc([C@]34OC[C@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87474
desired product
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc([C@]34OC[C@](CF)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87476
title compound
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc([C@]34OC[C@](CCl)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87478
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C(O)c2cc([C@]34OC[C@](COC(C)=O)(O3)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]4OC(C)=O)ccc2Cl)cc1
Reaction #87479
acetic acid (1R,2S,3S,4R,5S)-3,4-diacetoxy-1-acetoxymethyl-5-{4-chloro-3-[(4-ethoxy-phenyl)-hydroxy-methyl]-phenyl}6,8-dioxa-bicyclo[3.2.1]oct-2-yl ester
Yield 89.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C(=O)c2cc([C@]34OC[C@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87480
desired product
Yield 98.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc([C@]34OC[C@](COC(C)=O)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87490
product
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCOc1ccc(Cc2cc([C@]34OC[C@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87492
Acetic acid 2-{4-[2-chloro-5-((1S,2S,3S,4R,5S)-2,3,4-trihydroxy-1-hydroxymethyl-6,8-dioxa-bicyclo[3.2.1]oct-5-yl)-benzyl]-phenoxy}-ethyl ester
Yield 22.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCOc1ccc(Cc2cc([C@]34OC[C@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87493
desired compound
Yield 26.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCOc1ccc(Cc2cc([C@]34OC[C@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87494
desired product
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc([C@]34OC[C@](CF)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87496
title compound
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc([C@]34OC[C@](CCl)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87498
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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