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C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CC1OC
Reaction #6393
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #6394
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O[Si](C)(C)C(C)(C)C)C2C)C(OC)CC3C)CC1OC
Reaction #6399
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CC1OC
Reaction #6400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC2(O1)C(C)(C)CCCC2(C)O
Reaction #74885
2,6,10,10-tetramethyl-1-oxa-spiro[4.5]dec-3-ene-6-ol
収率 174.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OC1C2CC3C1OC(=O)C3C2C(=O)OC(C)(C)C
Reaction #162264
intended product
収率 70.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OC1C2CC3C1OC(=O)C3C2C(=O)O
Reaction #162265
intended product
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OC1C2CC3C1OC(=O)C3C2C(=O)Cl
Reaction #162266
7-Chlorocarbonyl-2-oxohexahydro-3,5-methano-2H-cyclopenta[b]furane-6-yl Methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC2(O1)C(C)(C)CCCC2(C)O
Reaction #184137
DOI: 10.1039/C8SC04228D
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1N=[N+]=[N-]
Reaction #185119
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OCC=Cc4ccccc4)C(OC)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #210866
DOI: 10.1039/C8SC04228D
C=CCOC1CCCCC1Oc1ccc(C#N)c(C(F)(F)F)c1
Reaction #230934
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OCC=Cc4ccccc4)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #235417
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OCCCc4ccccc4)C(OC)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #274560
DOI: 10.1039/C8SC04228D
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O[Si](C)(C)C(C)(C)C)C2C)C(OC)CC3C)CCC1O[Si](C)(C)C(C)(C)C
Reaction #280762
DOI: 10.1039/C8SC04228D
COC1C(OC(=O)C=CC=O)CCC2(CO2)C1C1(C)OC1CC=C(C)C
Reaction #287571
DOI: 10.1039/C8SC04228D
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #335444
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #335447
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1O[Si](C)(C)C(C)(C)C
Reaction #335462
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1O
Reaction #335463
title compound
収率 94.3%DOI: 10.6084/m9.figshare.5104873.v1
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