Substructure Search

1333189

CC(C)(C)[SiH2]OC(C)(C)C(CO[Si](C)(C)C(C)(C)C)COS(C)(=O)=O
Reaction #10767
methanesulfonic acid 3-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-propyl ester
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(CO)CO)c(-c2cccs2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10769
title compound
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(CO[Si](C)(C)C(C)(C)C)C(C)(C)O[SiH2]C(C)(C)C)c(C=O)cc1-c1cccs1
Reaction #10781
2-[3-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-propoxy]-4-methoxy-5-thiophen-2-yl-benzaldehyde
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(CO)CO)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10782
title compound
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)[O-]
Reaction #40270
acrylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)(C(=O)c1ccccc1)c1ccccc1
Reaction #50169
2,2-dimethyloxy-2-phenyl acetophenone
Yield 472.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2COC3(CCCC3)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59905
title compound
Yield 8.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2COC3(CCC3)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59906
title compound
Yield 6.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(C)(COC(C)=O)C(=O)O
Reaction #62796
2,2-bis-acetoxymethyl propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(COCCOCc2ccccc2)COC(C)(C)OC1
Reaction #65105
2,2-dimethyl-5-benzyloxyethoxymethyl-5-methyl-1,3-dioxane
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)CCOCC(C)(COCCS(=O)(=O)c2ccc(C)cc2)COCCS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #65107
1,1,1-tris(tosylethoxymethyl)ethane
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2OCC(C)(C(=O)O)CO2)cc1
Reaction #67492
title compound
Yield 74.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #71508
liquid
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CNC(=N)NCCCC1OCC2(CO1)COC(CCCNC(=N)NC#N)OC2
Reaction #81779
3,9-bis(3-cyanoguanidinopropyl)-2,4,8,10-tetraoxaspiro[5.5]undecane
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@@]12CO[C@@](c3ccc(Cl)c(Cc4ccc(O)cc4)c3)(O1)[C@H](O)[C@@H](O)[C@@H]2O
Reaction #87469
(1 S,2S,3S,4R,5S)-5-[4-chloro-3-(4-hydroxy-benzyl)-phenyl]-1-hydroxymethyl-6,8-dioxa-bicyclo[3.2.1]octane-2,3,4-triol
Yield 69.7%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 #87470
product
Yield 87.0%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
Yield 40.0%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
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