部分構造検索

14625

CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10230
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10232
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10234
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10236
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10238
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10240
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10242
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10244
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10246
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1C[C@](C)(O)Cc2cc3c(c(O)c21)C(=O)c1c(O)cc2c(c1C3=O)OC1OC2(C)[C@H](O)[C@@H](N(C)C)[C@@H]1O
Reaction #64004
7-0-methylnogarol
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)OC[C@@]12CO[C@@](c3ccc(Cl)c(Cc4ccc(OCC)cc4)c3)(O1)[C@H](O)[C@@H](O)[C@@H]2O
Reaction #87471
desired product
収率 40.0%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 #87477
desired product
収率 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
収率 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
収率 98.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)OC[C@@]12CO[C@@](c3ccc(Cl)c(Cc4ccc(OCC)cc4)c3)(O1)[C@H](O)[C@@H](O)[C@@H]2O
Reaction #87491
desired product
収率 40.0%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 #87497
desired product
収率 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
収率 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 #87500
desired product
収率 98.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H](C(OC(=O)c3ccccc3)C3CCCC3)C[C@H]2O1
Reaction #88982
[[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-cyclopentyl-methyl] benzoate
収率 80.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1O[C@H](C(OC(=O)c2ccccc2)C2CCCC2)C[C@H]1OC(C)=O
Reaction #88983
[cyclopentyl-[(2S,4R)-4,5-diacetoxytetrahydrofuran-2-yl]methyl] benzoate
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ