2-ethyl-1-hydroxy-4-phenylindane

CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #1354
desired product
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1cccc2c1CC(c1ccccc1)C2=O
Reaction #672359
aimed product
Выход 134.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
CCC1Cc2c(-c3ccccc3)cccc2C1O
Reaction #696700
aimed product
Выход 99.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #696701
aimed product
Выход 72.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #812375
desired product
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #813963
desired product
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
CCC1(c2ccccc2)Cc2ccccc2C1O
Reaction #1361564
aimed product
Выход 133.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_12
CCC1Cc2c(-c3ccccc3)cccc2C1O
Reaction #1576496
aimed product
Выход 99.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_10
CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #1576497
aimed product
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_10
CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #1672363
desired product
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #1847236
aimed product
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_01
CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #1867081
desired product
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_05
CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #2345251
desired product
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_08