子结构搜索

O=C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

OC1(c2cc3c(CCc4ccccc4)cccc3s2)O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #43684
2,3,4,6-tetra-O-benzyl-1-[4-(2-phenylethyl)benzo[b]-thiophene-2-yl]-D-glucopyranose
收率 86.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Cc2cccc3cc(C4(O)O[C@H](COCc5ccccc5)[C@@H](OCc5ccccc5)[C@H](OCc5ccccc5)[C@H]4OCc4ccccc4)sc23)cc1
Reaction #43688
title compound
收率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CC(O)(CC(=O)O)C(=O)O.[Na+]
Reaction #64831
monosodium citrate
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CC(O)(CC(=O)O)C(=O)O.[Na+]
Reaction #64832
monosodium citrate
DOI: 10.6084/m9.figshare.5104873.v1
OCc1cccc2ccccc12
Reaction #74461
1-naphthalenemethanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2(O)O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #74490
title compound
收率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCOC(=O)[C@H](C)N
Reaction #83174
dodecyl alaninate
收率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #83175
D-gluconamide
收率 215.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COCC2(COCc3ccc(OC)cc3)OC(=O)[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)cc1
Reaction #87466
(3R,4S,5S)-3,4,5-tris-benzyloxy-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-one
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(c2ccc(Cl)c(Cc3ccc(O)cc3)c2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #87468
product
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COCC2(COCc3ccc(OC)cc3)OC(=O)[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)cc1
Reaction #87486
(3R,4S,5S)-3,4,5-tris-benzyloxy-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-one
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(c2ccc(Cl)c(Cc3ccc(O)cc3)c2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #87488
product
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(Cc2cc(C3(O)OC(COCc4ccccc4)C(OCc4ccccc4)C(OCc4ccccc4)C3OCc3ccccc3)c(OC)cc2Cl)cc1
Reaction #188786
DOI: 10.1039/C8SC04228D
OC1(c2cc(Cc3cc4ccccc4s3)cc3ccccc23)OC(COCc2ccccc2)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #241533
DOI: 10.1039/C8SC04228D
CO[C@@]1(c2ccc(F)c(Cc3cc4ccccc4s3)c2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #306166
methyl 1-C-[3-(1-benzothien-2-ylmethyl)-4-fluorophenyl]-α-glucopyranoside
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)n1ccc2cc3c(cc21)[C@]1(OC3)O[C@H](COCc2ccccc2)[C@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #309111
titled compound
收率 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](N)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCc1ccccc1.O=C(O)[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #343644
GlcA Ile-Phe-OBzl
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(O)cc1
Reaction #498288
p-nitrophenol
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(O)cc1
Reaction #498289
p-nitrophenol
DOI: 10.6084/m9.figshare.5104873.v1
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