z-logo
Premium
Regioselektive Synthesen von 3,3′‐Bijuglon, Mamegakinon, Dianellinon, cyclo ‐Trijuglon, Xylospyrin und Trianellinon durch Phenol/Chinon‐Addition
Author(s) -
Brockmann Hans,
Laatsch Hartmut
Publication year - 1983
Publication title -
liebigs annalen der chemie
Language(s) - German
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 0170-2041
DOI - 10.1002/jlac.198319830310
Subject(s) - chemistry , phenol , medicinal chemistry , stereochemistry , organic chemistry
Durch regioselektive Phenol/Chinon‐Addition werden aus Juglon ( 1a ), 7‐Methyljuglon ( 1b ) und Stypandron ( 1c ) in Pyridin die Dimeren 3,3′‐Bijuglon ( 5a ), Mamegakinon ( 5c ), Dianellinon ( 5e ) und in Eisessig die cyclo‐Trimeren cyclo‐Trijuglon ( 12a ), Xylospyrin ( 12d ) und Trianellinon ( 12g ) synthetisiert.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom