SmI2/H2O/amine promoted reductive cleavage of benzyl-heteroatom bonds: optimization and mechanism
- 1 December 2009
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 65 (52) , 10856-10862
- https://doi.org/10.1016/j.tet.2009.10.086
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Studies toward the Total Synthesis of NominineThe Journal of Organic Chemistry, 2007
- Stereoselective synthesis of simplactone B via Prins cyclisationTetrahedron, 2007
- Electrophile‐Induced Ether Transfer: Stereoselective Synthesis of 2,4,6‐Trisubstituted TetrahydropyransAngewandte Chemie International Edition in English, 2007
- Synthesis of (±)‐ar‐MacrocarpeneSynthetic Communications, 2007
- Stereoselective 5-exo-trig radical cyclization in the enantioselective synthesis of PregabalinTetrahedron Letters, 2007
- Reductive cleavage of benzyl ethers with lithium naphthalenide. A convenient method for debenzylationTetrahedron Letters, 1997
- Selectivities in ionic reductions of alcohols and ketones with triethylsilane/trifluoroacetic acidTetrahedron Letters, 1997
- A practical synthesis of perdeuterated deoxyribose and deoxyribonucleosidesThe Journal of Organic Chemistry, 1993
- DEALUMINOXYLATION OF ALUMINUM ALLYL OR BENZYL ALKOXIDES AND DEOXYGENATION OF ALLYL ETHERS BY LITHIUM ALUMINUM HYDRIDE IN THE PRESENCE OF TITANIUM CATALYSTChemistry Letters, 1980
- 212. Reduction by dissolving metals. Part IIJournal of the Chemical Society, 1945