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1328361

CCCCCC1(CC[C@@H]2[C@H]3CC(=O)O[C@H]3C[C@H]2OC2CCCCO2)OCCO1
Reaction #50198
title compound ( 59 )
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC1(CC[C@@H]2[C@H](CC(=O)OC)[C@@H](O[SiH2]C(C)(C)C)C[C@H]2OC2CCCCO2)OCCO1
Reaction #50199
title compound ( 62 )
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC1(CC[C@@H]2[C@@H](CC(O)C(F)(F)C#CCCO[Si](C)(C)C(C)(C)C)[C@@H](O[SiH2]C(C)(C)C)C[C@H]2OC2CCCCO2)OCCO1
Reaction #50200
title compound ( 65 )
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC[C@H](O)[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](OC3CCCCO3)CC[C@@H]12
Reaction #55610
final product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCC(=O)[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](OC3CCCCO3)CC[C@@H]12
Reaction #55611
17β-tetrahydropyranyloxy-5α-androstan-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](NC)[C@H]2O)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #65120
N-demethylerythromycin A
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](NC)[C@H]2O)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #65121
N-demethylerythromycin A
収率 40.8%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)O)C1OC(C(C)C(O)C(C)C(=O)C(CC)C2OC3(C=CCC4(CCC(C)(C5CCC(O)(CC)C(C)O5)O4)O3)C(C)CC2C)C(C)CC1C
Reaction #74918
20-deoxynarasin
収率 71.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCCCC(C)(C)COC1CCCCO1)(CCCCC(C)(C)COC1CCCCO1)C(=O)OCC
Reaction #76271
2,2-bis-[5,5-dimethyl-6-(tetrahydropyran-2-yloxy)-hexyl]-malonic acid diethyl ester
収率 82.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCCCC(C)(C)CO)(CCCCC(C)(C)CO)C(=O)OCC
Reaction #76272
2,2-bis(6-hydroxy-5,5-dimethyl-hexyl)-malonic acid diethyl ester
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC2(OC1)OC1CC3C4CCC5CC(=O)C6OC6C5(C)C4CCC3(C)C1C2C
Reaction #174290
DOI: 10.1039/C8SC04228D
COC(=O)C(CC1CCCC1O)c1ccc(Cl)c(Cl)c1
Reaction #181618
DOI: 10.1039/C8SC04228D
CC1CCC2(OC1)OC1CC3C4CCC5CC(O)CCC5(C)C4C(O)C(O)C3(C)C1C2C
Reaction #210189
DOI: 10.1039/C8SC04228D
CC(=O)OC1C(O)C2C(CCC3CC(O[Si](C)(C)C(C)(C)C)CCC32C)C2CC3OC4(CCC(C)CO4)C(C)C3C21C
Reaction #213610
DOI: 10.1039/C8SC04228D
CCC(C)OC(=O)CC(C)CCCCCOC1CCCCO1
Reaction #214987
subtitle compound
収率 46.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1C(O[Si](C)(C)C)C2C(CCC3CC(O[Si](C)(C)C(C)(C)C)CCC32C)C2CC3OC4(CCC(C)CO4)C(C)C3C21C
Reaction #221395
DOI: 10.1039/C8SC04228D
OC(CCc1ccccc1)CCC1C(O)CC2OC(O)CC21
Reaction #239510
DOI: 10.1039/C8SC04228D
CCC(C)OC(=O)CC(C)CCCCCOC1CCCCO1
Reaction #256351
DOI: 10.1039/C8SC04228D
CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(N(C)C)C2O)C(C)(O)CC(C)C(=O)C(C)C(O)C1(C)O
Reaction #276742
DOI: 10.1039/C8SC04228D
C=C1C[C@@]23CC[C@H]4[C@@](C)(CCC[C@@]4(C)C(=O)O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@H]2CC[C@]1(O[C@@H]1O[C@H](C)[C@@H](O)[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O)C3
Reaction #310524
rebaudioside C
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
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