子结构搜索

1087015

O=C1CCCCCO1.O=C1COCCO1
Reaction #2356
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2357
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2358
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2359
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1COC[C@H]1OC(=O)C(C)Cl
Reaction #3176
(±)-(3R,4S)-4-Acetoxy-3-(2-chloropropionyloxy)tetrahydrofuran
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)C(=O)OC)cc1
Reaction #5822
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(O[C@@H]2SC[C@@H](O)[C@H](O)[C@H]2O)cc1
Reaction #6131
expected product
收率 81.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1O[C@@H]1SC[C@@H](O)[C@H](O)[C@H]1O
Reaction #6143
expected product
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCCOC(=O)C1CC1
Reaction #7072
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC(O)CO
Reaction #8282
title compound
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC(O)CO[Si](C)(C)C(C)(C)C
Reaction #8283
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=NO)c1ccc2c(c1O)OC(CO)CO2
Reaction #56745
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccc3c(c2o1)OC(CO)CO3
Reaction #56746
[2-Methyl-7,8-dihydro[1,4]dioxino[2,3-g][1,3]benzoxazol-8-yl]methanol
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc2cccc(C3COC(C)(C)O3)c2c1C
Reaction #57604
4-(2,2-dimethyl-1,3-dioxolan-4-yl)-3-methylbenzofuran-2-carboxylic acid ethyl ester
收率 973.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](O)CO[Si](C)(C)C(C)(C)C
Reaction #59831
title compound
收率 59.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC1CC(O)C(O)C1)c1ccc([N+](=O)[O-])cc1
Reaction #69434
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCC
Reaction #71258
Cetyl Stearate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)O.OCCN(CCO)CCO
Reaction #71259
Triethanolamine Stearate
DOI: 10.6084/m9.figshare.5104873.v1
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #73939
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(C)=C/c1cc(F)c(Oc2ccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])cc2)c(F)c1
Reaction #73969
title compound
收率 47.1%DOI: 10.6084/m9.figshare.5104873.v1
第 1 页下一页