子结构搜索

41709

CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@@H]2O[C@@H]21
Reaction #65672
5'-O-(t-butyldimethylsilyl)-2',3'-anhydroadenosine
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC[C@@H]1C[C@@H](O)[C@H](n2cnc3c(N)ncnc32)O1
Reaction #65673
title compound
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1COC[C@H]1NCc1ccccc1
Reaction #168346
trans-4-(benzylamino) tetrahydrofuran-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
OC1COCC1OCc1ccccc1
Reaction #209967
DOI: 10.1039/C8SC04228D
OC1COCC1Oc1ccc(Br)cc1
Reaction #254656
DOI: 10.1039/C8SC04228D
OC1COCC1c1ccc(F)cc1
Reaction #282664
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@@H]2O[C@@H]21
Reaction #322152
5'-O-(t-butyldimethylsilyl)-2',3'-anhydroadenosine
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC[C@@H]1C[C@@H](O)[C@H](n2cnc3c(N)ncnc32)O1
Reaction #322153
title compound
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(S[C@@H]2COC[C@H]2O)cc(C(C)(C)C)c1O
Reaction #362580
trans-4-[[3,5-bis(1,1-Dimethylethyl)-4-hydroxyphenyl]thio]tetrahydro-3-furanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NNC1COCC1O
Reaction #378160
DOI: 10.1039/C8SC04228D
C=CCCCC1COCC1O
Reaction #406833
DOI: 10.1039/C8SC04228D
C=CCO[C@@H]1COC[C@H]1O
Reaction #457498
trans-3-allyloxy-4-hydroxytetrahydrofuran
DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1COC[C@H]1OCc1ccccc1
Reaction #457499
trans-3-benzyloxy-4-hydroxytetrahydrofuran
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]1(CC(F)(F)F)OC(=O)C(Oc2ccc(Br)cn2)=C1c1ccc(S(C)(=O)=O)cc1
Reaction #463544
(5R)-3-(5-bromo-2-pyridyloxy)-4-(4-methylsulfonylphenyl)-5-methyl-5-(2,2,2-trifluoroethyl)-5H-furan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)Nc2c(Cl)cncc2Cl)cc1OC1COCC1O
Reaction #467916
title compound
收率 27.1%DOI: 10.6084/m9.figshare.5104873.v1
O[C@H]1COC[C@@H]1c1ccc(F)cc1
Reaction #488977
title compound
收率 39.7%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=N[C@@H]1COC[C@H]1O
Reaction #500410
title compound
收率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1COCC1n1cc(-c2ccc3cnc(Cl)cc3c2)cn1
Reaction #610241
title compound
收率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc(C)c(C2COCC2O)c1Br
Reaction #750065
DOI: 10.1039/C8SC04228D
COC1OC(COCc2ccccc2)C(F)C1O
Reaction #750728
DOI: 10.1039/C8SC04228D
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