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C1CC(OC1)CCO

CC(=O)O[C@H]1[C@H](n2cc(C)c(=O)[nH]c2=O)OC(COC(=O)c2ccccc2)(COC(=O)c2ccccc2)[C@@H]1OCc1ccccc1
Reaction #6873
nucleoside
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6882
material
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6883
material
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(/C=C/[C@@H]1[C@H]2CC(=O)O[C@H]2C[C@H]1OC1CCCCO1)O[Si](C)(C)C(C)(C)C
Reaction #50191
title compound ( 46 )
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1O[C@H]2[C@H](OC(=O)[C@H]2O)[C@H]1O
Reaction #64339
methyl β-D-glucofuranosidurono-6, 3-lactone
Выход 19.3%DOI: 10.6084/m9.figshare.5104873.v1
COC1=CC(=O)C2C3CCC(O3)C12
Reaction #69961
5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Выход 84.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cnc(Cl)cc2C)C(=O)C2C3CCC(O3)C12
Reaction #69963
4-(6-chloro-4-methyl-pyridin-3-yl)-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Выход 64.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)ncc1C1C(=O)C2C3CCC(O3)C2C1=O
Reaction #69964
4-(6-chloro-4-methyl-pyridin-3-yl)-10-oxa-tricyclo[5.2.1.0*2,6*]decane-3,5-dione
Выход 91.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)C2C3CCC(O3)C2C(=O)Cl)CC1
Reaction #73456
3-(4-Methylpiperazine-1-carbonyl)-7-oxa-bicyclo[2,2,1]heptane-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(=O)O[C@H]1CO[C@H]2[C@@H]1OC[C@H]2OC(=O)CCCCCCC
Reaction #90211
Isosorbide Dicaprylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2C3CCC(O3)C12
Reaction #155664
product
Выход 50.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(=O)c2[nH]c(C3(O)CC4OC(C3)C(C(=O)OC)C4C(=O)OC)nc2n(CCC)c1=O
Reaction #198757
DOI: 10.1039/C8SC04228D
CCCCCCCC(C=CC1C(O)CC2OC(O)CC21)OC1CCCCO1
Reaction #207394
DOI: 10.1039/C8SC04228D
CCCCC(F)(F)C(=O)C=CC1C(OC(=O)c2ccccc2)CC2OC(=O)CC21
Reaction #208965
DOI: 10.1039/C8SC04228D
CN1CCN(C(=O)C2C3CCC(O3)C2C(=O)Cl)CC1
Reaction #212138
DOI: 10.1039/C8SC04228D
O=c1nc[nH]c2c1ncn2[C@@H]1O[C@H](COP(=O)([O-])[O-])[C@@H](O)[C@H]1O.[Na+].[Na+]
Reaction #214229
ribotide
DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC(C(COCc2ccccc2)OS(C)(=O)=O)OC1=O
Reaction #221425
DOI: 10.1039/C8SC04228D
O=C1CC2C(CC(O)C2CCC(F)(F)COc2ccccc2)O1
Reaction #233665
DOI: 10.1039/C8SC04228D
CCCCCC(O)C=CC1C(O)CC2OC(=CCCCC(=O)OCCN(CC)CC)CC21
Reaction #235004
DOI: 10.1039/C8SC04228D
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