子结构搜索

675950

CC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64079
t-butyl (3S)-2-methyl-3-hydroxybutanoate
收率 43.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64085
t-butyl (3S )-2-ethyl-3-hydroxybutanoate
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64086
t-butyl (3S)-2-allyl-3-hydroxybutanoate
收率 45.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](O)C(C)C(=O)OC
Reaction #64087
methyl (3S)-2-methyl-3-hydroxypentanoate
收率 77.8%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H](CBr)c1cccc(Cl)c1
Reaction #444908
(R)-2-bromo-1-(3-chlorophenyl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)OC1=C(c2ccc(C)cc2)C(=O)CC(C)(C)C1
Reaction #457572
desired product
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCCCCCC
Reaction #459548
stearic anhydride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1[C@H]2[C@H]([C@@H]3[C@@H](O)[C@@H]4[C@H]([C@H](C)C=C5OC(=O)[C@@](C)(O)[C@@]54C)[C@@]3(C)[C@H]1OC(C)=O)[C@@H](O)C(=O)[C@H]1C[C@@H]3O[C@@H]3[C@H](OC(C)=O)[C@]21C
Reaction #612472
taccalonolide B
收率 68.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@H]2[C@H]3[C@H]([C@H](OC(C)=O)[C@H](OC(C)=O)[C@]2(C)[C@@H]2[C@@H]1[C@]1(C)C(=C[C@H]2C)OC(=O)[C@@]1(C)O)[C@]1(C)[C@H](C[C@@H]2O[C@@H]2[C@@H]1OC(C)=O)C(=O)[C@@H]3O
Reaction #612473
taccalonolide A
DOI: 10.6084/m9.figshare.5104873.v1
C=COC(=O)CCCCCCCCCCC
Reaction #661231
lauric acid vinyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=COC(=O)CCCCCCCCCCC
Reaction #805743
lauric acid vinyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=COC(=O)CCCCCCCCCCCCCCCCC
Reaction #902301
DOI: 10.1039/C8SC04228D
C=COC(=O)CCCCCCCCCCC
Reaction #1129015
lauric acid vinyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=COC(=O)CCCCCCCCCCC
Reaction #1160666
vinyl laurate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)OC(=O)CCCCCCCCCCCCCCCCC
Reaction #1241465
isopropenyl stearate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@@H]1[C@H]2CC(CCCCC(=O)OC3=C(C)C=CC(=NNC(N)=O)C3)S[C@H]2C[C@H]1O
Reaction #1251342
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)OC1=CC(=O)OC(C)C1
Reaction #1252934
4-dodecanoyloxy-6-methyl-5,6-dihydro-2-pyrone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)c2ccccc21
Reaction #1255308
Phthalic Anhydride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)OC[C@H]1O[C@H](Oc2ccc([N+](=O)[O-])cc2)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #1362712
4-nitrophenyl 6-O-palmitoyl-α-D-glucopyranoside
收率 84.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CN1CCCC1=O.C=COC(=O)CCCCCCCCCCC
Reaction #1526130
N-Vinylpyrrolidone vinyl laurate
DOI: 10.6084/m9.figshare.5104873.v1
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