Highly diastereoselective dielsalder reaction mediated by a chiral auxiliary derived from amino indanol: The role of conformation on diastereoselectivity

DOI: 10.1016/0040-4039(95)01584-5

Source and publish data:

Tetrahedron Letters p. 7619 - 7622 (1995)

Update date:2022-08-04

Topics:

Authors:

Davies, Ian W.

Senanayake, Chris H.

Castonguayi, Laurie

Larsen, Robert D.

Verhoeven, Thomas R.

Reider, Paul J.

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Article abstract of DOI:10.1016/0040-4039(95)01584-5

The oxazolidinone 2 derived from amino indanol 1 functions as a very efficient chiral auxiliary for the Diels-Alder reaction. The effect of conformation has been explored using a range of constrained phenyl glycinol analogues.

Full text of DOI:10.1016/0040-4039(95)01584-5

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