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  4. The Diels-Alder Chemoselectivity of 3,4,6,7-Tetramethylidenebicyclo[3.2.1]Octane-2-Exo,8-Syn-Diyl Derivatives
 
research article

The Diels-Alder Chemoselectivity of 3,4,6,7-Tetramethylidenebicyclo[3.2.1]Octane-2-Exo,8-Syn-Diyl Derivatives

Claret, F.
•
Razaname, A.
•
Vogel, P.  
1992
Helvetica Chimica Acta

Strong dienophiles prefer to add onto the diene moiety attached at C(2),C(3) of 2,3,6,7-tetramethylidenebicyclo[3,2,1]octane ((+/-)-1; see Scheme 1), whereas in the case of 3,4,6,7-tetramethylidenebicyclo[3.2.1]octane-2-exo,8-syn-diyl derivatives. the diene moiety at C(6),C(7) reacts faster than that at C(3),C(4), as long the bulk of the 8-syn-substituent is large enough (see Schemes 2 and 3).

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Type
research article
DOI
10.1002/hlca.19920750412
Author(s)
Claret, F.
Razaname, A.
Vogel, P.  
Date Issued

1992

Published in
Helvetica Chimica Acta
Volume

75

Issue

4

Start page

1085

End page

1094

Subjects

Naphthocyclinone series

•

antibiotics

Note

Univ lausanne,chim sect,rue barre 2,ch-1005 lausanne,switzerland.

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LGSA  
Available on Infoscience
November 9, 2005
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/219658
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