7-(1-adamantyl)-6-hydroxy-2-bromonaphthalene

Brc1ccc2cc(OCc3ccccc3)c(C34CC5CC(CC(C5)C3)C4)cc2c1
Reaction #1228
expected compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Fc1ccc(COc2cc3ccc(Br)cc3cc2C23CC4CC(CC(C4)C2)C3)cc1
Reaction #1238
expected compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)Oc1cc2ccc(Br)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #1239
7-(1-adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Brc1ccc2cc(OCc3ccccc3)c(C34CC5CC(CC(C5)C3)C4)cc2c1
Reaction #705661
7-(1-adamantyl)-6-benzyloxy-2-bromonaphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
Fc1ccc(COc2cc3ccc(Br)cc3cc2C23CC4CC(CC(C4)C2)C3)cc1
Reaction #705670
expected compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
COCCOCOc1cc2ccc(Br)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #705673
7-(1-adamantyl)-6-methoxyethoxymethoxy-2-bromonaphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
CCCCCCCOc1cc2ccc(Br)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #705674
7-(1-adamantyl)-6-heptyloxy-2-bromonaphthalene
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
Brc1ccc2cc(OCc3ccccc3)c(C34CC5CC(CC(C5)C3)C4)cc2c1
Reaction #787302
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Fc1ccc(COc2cc3ccc(Br)cc3cc2C23CC4CC(CC(C4)C2)C3)cc1
Reaction #1033662
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCCCCCCOc1cc2ccc(Br)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #2063345
7-(1-adamantyl)-6-heptyloxy-2-bromonaphthalene
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_05
Brc1ccc2cc(OCc3ccccc3)c(C34CC5CC(CC(C5)C3)C4)cc2c1
Reaction #2218074
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
CCCCCCCOc1cc2ccc(Br)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #2242934
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)