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- A stereochemical test for ether-oxygen participation and oxonium ion formation in the acetolysis of 3-tetrahydropyranyl brosylate. Ian R. Dunkin, Alan J. Paul, Colin J. Suckling, Edward Valente, Hamish C. S. Wood
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 1323
- Stereoselective synthesis of tetrahydropyran-3-ones by rearrangement of oxonium ylides generated from metal carbenoids. J. Stephen Clark, Gavin Whitlock, Shende Jiang, Ngozi Onyia
, Chem. Commun.
, 2003
, 2578
- Regiospecific enolates from tetrahydropyran-3-one. Synthetic equivalents of a thermodynamically and kinetically disfavoured enolate isomer. Paul Cox, Simon Lister, Timothy Gallagher
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 3151
- Intramolecular addition of acyl radicals to α-substituted vinylogous carbonates: demonstrating the effect of ring size on acyclic stereocontrol. P. Andrew Evans, Sushil Raina, Khalid Ahsan
, Chem. Commun.
, 2001
, 2504
- Synthesis of the namenamicin A–C disaccharide: towards the total synthesis of namenamicin. David S. Weinstein, K. C. Nicolaou
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 545
- Index pages
, J. Chem. Soc., Perkin Trans. 1
, 1990
, A001
- Stereoselective synthesis of cis- and trans-2,6-disubstituted 5,6-dihydro-2H-pyrans based on 1,5-asymmetric induction in reactions between allylstannanes and aldehydes promoted by tin(IV) chloride. Robert J. Maguire, Eric J. Thomas
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 2487
- Synthesis of stable prostacyclin analogues from 2,3-disubstituted bicyclo[3.2.0]heptan-6-ones. Roger F. Newton, Alan H. Wadsworth
, J. Chem. Soc., Perkin Trans. 1
, 1982
, 823
- Some limitations of an approach to the assembly of bryostatins by ring-closing metathesis. Raphaël Dumeunier, Thomas Gregson, Somhairle MacCormick, Hiroki Omori, Eric J. Thomas
, Org. Biomol. Chem.
, 2017
, 15
, 2768
- Reductive cleavage as a route to carbohydrate enolates. Applications to the synthesis of C-linked disaccharides. Hayley M. Binch, Andrew M. Griffin, Sabine Schwidetzky, Michael V. J. Ramsay, Timothy Gallagher, Frieder W. Lichtenthaler
, J. Chem. Soc., Chem. Commun.
, 1995
, 967