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  4. The simultaneous double Diels-Alder addition of 1,1-bis(3,5-dimethylfur-2-yl)ethane; Toward a new, asymmetric synthesis of long-chain polypropionate fragments and analogues
 
research article

The simultaneous double Diels-Alder addition of 1,1-bis(3,5-dimethylfur-2-yl)ethane; Toward a new, asymmetric synthesis of long-chain polypropionate fragments and analogues

Marchionni, C.
•
Vogel, P.  
•
Roversi, P.
1996
Tetrahedron Letters

The double cycloaddition of 1,1-bis(3,5-dimethylfur-2-yl)ethane to diethyl (E,E)-4-oxohepta-2,5-diene-1,7-dioate gave a single bis-adduct, the hydroboration of which with IpcBH(2) allows the creation of optically active polycyclic systems that are potential precursors of long-chain polypropionate fragments. (C) 1996 Published by Elsevier Science Ltd

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Type
research article
DOI
10.1016/0040-4039(96)00771-X
Author(s)
Marchionni, C.
Vogel, P.  
Roversi, P.
Date Issued

1996

Publisher

Elsevier

Published in
Tetrahedron Letters
Volume

37

Issue

24

Start page

4149

End page

4152

Subjects

Products

•

esters

Note

Univ lausanne,bch,sect chem,ch-1015 lausanne,switzerland. univ milan,dipartimento chim fis & elettrochim,i-20133 milan,italy.

Editorial or Peer reviewed

REVIEWED

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EPFL units
LGSA  
Available on Infoscience
November 9, 2005
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/219716
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