137517-52-3Relevant academic research and scientific papers
Synthesis of trans-4a-aryl-6-oxodecahydroiso-quinolines
Kawamura, Kuniaki,Kawai, Koji,Miyamoto, Toru,Ooshima, Koji,Nagase, Hiroshi
, p. 267 - 283 (2007/10/03)
General and short synthesis of trans-4a-aryl-6-oxodecahydroiso-quinolines was described. In particular, the synthesis of 2-cyclopropylmethyl-4a-(3-hydroxyphenyl)-trans-6-oxodecahydroisoquinoline (12), one of the remarkably useful molecule as an opioid message structural part, was attained in only seven steps. The key step in this synthetic approach was 1,4-conjugate addition of aryl moiety to sterically hindered enones (2).
Synthesis, Antinociceptive Activity, and Opioid Receptor Profiles of Substituted trans-3-(Decahydro- and Octahydro-4a-isoquinolinyl)phenols
Judd, Duncan B.,Brown, Dearg S.,Lloyd, Jane E.,McElroy, Andrew B.,Scopes, David I. C.,et al.
, p. 48 - 56 (2007/10/02)
A series of trans-3-(6- and 7-substituted-decahydro-4a-isoquinolinyl)phenols and trans-3-(octahydro-4a-isoquinolinyl)phenols have been synthesized as potential opioid analgesics.Using a combination of in vitro and in vivo test systems, the receptor profil
