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.

doi:10.1016/0040-4039(96)00771-X

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

Type

research article

DOI

10.1016/0040-4039(96)00771-X

Authors

Marchionni, C.

•

Vogel, P.

•

Roversi, P.

Publication date

1996

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.

Peer reviewed

REVIEWED

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