z-logo
Premium
Synthese mittlerer und großer Ringe, XXIX. Oxidation von 3,4‐Hexamethylenfuran zu 2,9‐Dioxodecan‐10‐olid
Author(s) -
Molkentin Joachim,
Goepfert Andreas,
Tochtermann Werner
Publication year - 1991
Publication title -
chemische berichte
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 0009-2940
DOI - 10.1002/cber.19911240828
Subject(s) - chemistry , ozonolysis , butenolide , yield (engineering) , stereochemistry , organic chemistry , materials science , metallurgy
Synthesis of Medium and Large Rings, XXIX. ‐ Oxidation of 3,4‐Hexamethylenefuran to 2,9‐Dioxodecan‐10‐olide 3,4‐Hexamethylenefuran ( 1 a ) is oxidized by various methods to give the butenolide 2. Ozonolysis of 2 affords 2,9‐dioxodecan‐10‐olide ( 3 ) in 80% yield.

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