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
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom