ChemInform Abstract: Dichlorination of (Hexadehydro-Diels-Alder Generated) Benzynes and a Protocol for Interrogating the Kinetic Order of Bimolecular Aryne Trapping Reactions.

ChemInform ◽  
2014 ◽  
Vol 45 (23) ◽  
pp. no-no
Author(s):  
Dawen Niu ◽  
Tao Wang ◽  
Brian P. Woods ◽  
Thomas R. Hoye
1985 ◽  
Vol 40 (11) ◽  
pp. 1575-1579 ◽  
Author(s):  
Hans Hofmann ◽  
Gerhard Löw ◽  
Armin Haag

4-Cyano- and 4-Carbomethoxy-3,4-dihydro-2H-l,5-benzodioxepin-3-one (1a and 1b) have been converted to the corresponding enol-toluenesulfonates 2a and 2b, respectively. Reaction of 2a and 2b with base led to the heterocyclic allenes 3a resp. 3b, which could be trapped by Diels-Alder-reaction with furane, yielding the cycloadducts 4a and 4b.


Synlett ◽  
1989 ◽  
Vol 1989 (01) ◽  
pp. 30-32
Author(s):  
Thomas V. Lee ◽  
Alistair J. Leigh ◽  
Christopher B. Chapleo

2009 ◽  
Author(s):  
Pedro Mancini ◽  
Maria Kneeteman ◽  
Claudia Della Rosa
Keyword(s):  

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