Substructure Search

OC(c1ccccc1)c1cccc(C2OCCO2)c1

CCOc1ccc(C(O)c2cc([C@]34OC[C@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87477
desired product
Yield 93.0%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 #87497
desired product
Yield 93.0%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 #87499
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
OC(c1ccccc1)c1cccc(C2OCCO2)c1
Reaction #181952
DOI: 10.1039/C8SC04228D
OC(c1cccc(C2OCCO2)c1)c1cccc(C(F)(F)F)c1
Reaction #217530
(3-(1,3-dioxolan-2-yl)phenyl)[3-(trifluoromethyl)phenyl]-methan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
OC(c1cccc(C2OCCO2)c1)c1cccc(C(F)(F)F)c1
Reaction #370432
DOI: 10.1039/C8SC04228D
O=C(c1ccccc1)c1cccc(C2OCCO2)c1
Reaction #399878
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1c(C(O)c2ccc(F)c(C3OCCO3)c2)ccc2cccnc12
Reaction #600879
title compound
Yield 74.0%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 #713033
desired product
Yield 93.0%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 #713035
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
Nc1ccc(C2(c3ccc(Cl)cc3)OCCO2)cc1C(O)c1cccc(Cl)c1
Reaction #785251
DOI: 10.1039/C8SC04228D
COc1ccc(C2CSc3cc(OC)ccc3C2(O)c2cccc(C3OCCO3)c2)cc1
Reaction #900299
DOI: 10.1039/C8SC04228D
Cc1c(NC(=O)CC(C)(C)C)cc2c(c1C)OC(C)(C)C2(O)c1cccc(C2OCCO2)c1
Reaction #923096
DOI: 10.1039/C8SC04228D
Nc1ccc(C2(c3ccc(Cl)cc3)OCCO2)cc1C(O)c1cccc(Cl)c1
Reaction #947965
2-amino-α-(3-chlorophenyl)-5-[2-(4-chlorophenyl)-1,3-dioxolan-2-yl]-benzenemethanol
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)Nc1ccc(C2(c3ccc(Cl)cc3)OCCO2)cc1C(O)c1cccc(Cl)c1
Reaction #947966
intermediate 10
DOI: 10.6084/m9.figshare.5104873.v1
O=C1COC(c2cccc(Cl)c2)c2cc(C3(c4ccc(Cl)cc4)OCCO3)ccc2N1
Reaction #947967
5-(3-chlorophenyl)-7-[2-(4-chlorophenyl)-1,3-dioxolan-2-yl]-1,5-dihydro-4,1-benzoxazepin-2(3H)-one
Yield 51.8%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)c2ccc(Cl)cc2)cc1C(SCC(=O)O)c1cccc(Cl)c1
Reaction #947974
[[[2-amino-5-(4-chlorobenzoyl)phenyl](3-chlorophenyl)methyl]thio]-acetic acid
Yield 95.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C(O)c2cc([C@]34OC[C@](C(C)O)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #1142803
title compound 29
Yield 20.1%DOI: 10.6084/m9.figshare.5104873.v1
FC(c1ccccc1)c1cccc(C2OCCO2)c1
Reaction #1210185
DOI: 10.1039/C8SC04228D
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