z-logo
open-access-imgOpen Access
Cycloaddition Reaction of Ethyl Thioxoacetate and the Dienamine Derived from Pummerer′s Ketone
Author(s) -
Brahim Kouissa,
Nourreddine Beghidja,
Karim Bouchouit,
Youcef Mechehoud
Publication year - 2012
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.436
H-Index - 50
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2013/813451
Subject(s) - chemistry , ketone , pummerer rearrangement , cycloaddition , organic chemistry , stereochemistry , catalysis , acetic anhydride
The objective of this work is to study the regio- and stereochemistry of the cycloadducts obtained from the treatment of ethyl thioxoacetate and the dienamine derived from Pummerer's ketone

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

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