The high pressure mediated intramolecular diels-alder reaction of furans: Factors controlling cycloaddition with monoactivated dienophiles.

Tetrahedron Letters

Volumn 29, Issue 39, 1988, Pages 5017-5020

  Harwood, Laurence M ^a   Leeming, Sarah A ^a   Isaacs, Neil S ^b   Jones, Geraint ^c   Pickard, John ^a   Thomas, Royston M ^a   Watkin, David ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF READING   (United Kingdom)

^c AKZO NOBEL CENTRAL RESEARCH   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0011392609     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)80668-1     Document Type: Article

References (20)

1. The intramolecular Diels–Alder reaction: recent advances and synthetic applications
2. Molecular design by intramolecular Diels-Alder reactions of furans.
3. The Intramolecular Diels-Alder Furan Approach in Synthesis : 11-oxatricyclo|6.2.1.01,6|undec-9-en-5-one