Synthetic Applications (I) of the Tandem [2,3]-Wittig-Anionic Oxy-Cope Rearrangement: Stereoselective Disubstituted Tetrahydropyran Synthesis by Electrophile Initiated Cyclisation

Author:

Greeves Nicholas,Lee Wai-Man

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Preceeding paper in this issue, Greeves, N.; Lee, W.M. Tetrahedron Lett., 1997, 38, 6445.

2. Greeves, N.; Vines, K.J. J. Chem. Soc., Chem. Commun., 1994, 1469–1470.

3. a) Bedford, S.B.; Bell, K.E.; Fenton, G.; Hayes, C.J.; Knight, D.W.; Shaw, D. Tetrahedron Lett., 1992, 33, 6511–6514. b) Grote, J.; Harigaye, Y.; Williams, D.R. Tetrahedron Lett., 1984, 25, 5231–5234.

4. Iodoetherification of 4-penten-1,3-diols: stereoselective synthesis of cis 2-iodomethyl-3-hydroxytetrahydrofurans

5. Iodine monobromide (IBr) at low temperature: enhanced diastereoselectivity in electrophilic cyclizations of homoallylic carbonates

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