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1300741

OCc1ccc2ccccc2c1OCc1ccccc1
Reaction #76229
[1-(benzyloxy)-2-naphthyl]methanol
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1ccc2c(OCc3ccccc3)cccc2c1OCc1ccccc1
Reaction #157188
1,5-Bis-benzyloxy-naphthalene-2-carboxylic Acid Benzyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1ccc2ccc(OCc3ccccc3)cc2c1OCc1ccccc1
Reaction #157189
1,7-Bis-benzyloxy-naphthalene-2-carboxylic Acid Benzyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc2c(OCc3ccccc3)cccc2c1OCc1ccccc1
Reaction #157190
creamy white solid
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1ccc2ccccc2c1OCc1ccccc1
Reaction #157191
yellow-orange viscous product
Ausbeute 38.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc2ccccc2c1OCc1ccccc1
Reaction #157192
1-Benzyloxy-naphthalene-2-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)NC(=O)c1cc(F)c2ccccc2c1OCc1ccc(C(F)(F)F)cc1
Reaction #243648
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(N2C(=O)c3c(c(OCc4ccccc4)c4ccccc4c3OCC)C2=O)c(F)c1
Reaction #260303
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(C(=O)OCC)c(OCc2ccccc2)c2ccccc2c1OCc1ccccc1
Reaction #309604
title compound
Ausbeute 109.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(C(=O)O)c(OCc2ccccc2)c2ccccc2c1OCc1ccccc1
Reaction #309605
title compound
Ausbeute 89.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(N2C(=O)c3c(c(OCc4ccccc4)c4ccccc4c3OCc3ccccc3)C2=O)cc1
Reaction #309608
title compound
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(=O)OCC)c(OCc2ccccc2)c2ccccc2c1OCC
Reaction #309612
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(C(=O)O)c(C(=O)O)c(OCc2ccccc2)c2ccccc12
Reaction #309613
title compound
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(N2C(=O)c3c(c(OCc4ccccc4)c4ccccc4c3OCC)C2=O)cc1
Reaction #309614
title compound
Ausbeute 74.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(=O)OC)c(OCc2ccccc2)c2c(OCc3ccccc3)ccc(OCc3ccccc3)c2c1OCc1ccccc1
Reaction #461166
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)c2c1c(OCc1ccccc1)c1c(OCc3ccccc3)ccc(OCc3ccccc3)c1c2OCc1ccccc1
Reaction #461167
title compound
Ausbeute 76.8%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc2ccccc2c1OCc1ccccc1
Reaction #520331
[1-(benzyloxy)-2-naphthyl]methanol
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2ccc(C(C)(C)O)c(OCc3ccccc3)c12
Reaction #741876
captioned compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1ccc2cccc(C)c2c1OCc1ccccc1
Reaction #741877
captioned compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCC#CC(O)c1ccc2ccccc2c1OCc1ccccc1
Reaction #791051
title compound
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
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