子结构搜索

1130728

CC1(C)O[C@@H]2O[C@H](CO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)C[C@@H]2O1
Reaction #88998
[(3aS,5S,6aS)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methoxy-tert-butyl-diphenyl-silane
收率 88.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CC2(CCNC2)c2cc(Cl)ccc21
Reaction #171166
1-methanesulfonyl-5-chloro-spiro[indoline-3,3′-pyrrolidine]
收率 85.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cc3c(ccc4c5ccccc5cnc34)c(CCCO)c2c1OCc1ccccc1
Reaction #189904
DOI: 10.1039/C8SC04228D
COc1ccc(Cc2cc(C3(O)OC(C)C(O)C(O)C3O)ccc2Cl)cc1
Reaction #202900
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(C1)OCCC2(C)C
Reaction #265128
DOI: 10.1039/C8SC04228D
COc1ccc2c(c(CCCO)nc3c4ccccc4ccc23)c1OCc1ccccc1
Reaction #269579
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(c2nc(C(F)(F)F)c(Cl)cc2N)CC1
Reaction #304454
3-amino-5-chloro-6-trifluoromethyl-3′,4′,5′,6′-tetrahydro-2′H-[2,4′]bipyridinyl-1′-carboxylic acid tert-butyl ester
收率 96.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)CC[Si]([Si](C)(C)C)([Si](C)(C)C)[Si](C)(C)C
Reaction #364836
title compound
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OC(C)(C)CC[Si]([Si](C)(C)C)([Si](C)(C)C)[Si](C)(C)C
Reaction #364837
title compound
收率 67.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CC[Si]([Si](C)(C)C)([Si](C)(C)C)[Si](C)(C)C)OC(=O)C1CC2C=CC1C2
Reaction #364838
title compound
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2nc(C(F)(F)F)c(Cl)cc2N)CC1
Reaction #376697
DOI: 10.1039/C8SC04228D
Nc1ncnc2c1ncn2[C@@H]1C[C@H](OC(=O)c2ccccc2)[C@H](COC(=O)c2ccccc2)O1
Reaction #500283
4
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1ncn2[C@@H]1C[C@H](OC(=O)c2ccccc2)[C@H](COC(=O)c2ccccc2)O1
Reaction #500848
4
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1ncn2[C@@H]1C[C@H](OC(=O)c2ccccc2)[C@H](COC(=O)c2ccccc2)O1
Reaction #583746
4
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC2C=CC1C(=O)C(C(=O)c1ccc(C(F)F)nc1C)C2=O
Reaction #590106
3-(2-Methyl-6-difluoromethyl-pyridine-3-carbonyl)-2,4-dioxo-bicyclo[3.2.2]non-8-ene-6-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(C1)OCCC2(C)C
Reaction #591618
tert-butyl 4,4-dimethyl-1-oxa-7-azaspiro[4.4]nonane-7-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CC[C@@H]2C[C@H]1C(=O)O2
Reaction #617885
compound 3
收率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(C1)OCCC2(C)C
Reaction #645158
tert-butyl 4,4-dimethyl-1-oxa-7-azaspiro[4.4]nonane-7-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #722702
crude product
收率 21.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c(CCCO)nc3c4cc5c(cc4ccc23)OCO5)c1OCc1ccccc1
Reaction #722703
2,3-(methylenedioxy)-6-(3-hydroxypropyl)-7-benzyloxy-8-methoxy-benzo[c]phenanthridine
收率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
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