Chlorotrimethylsilane as a Mild and Effective Source of Acid Catalyst in Reductive Benzylation

This publication has 9 references indexed in Scilit:

• TMSCl as a Mild and Effective Source of Acidic Catalysis in Fischer Glycosidation and Use of Propargyl Glycoside for Anomeric Protection
  Bioscience, Biotechnology, and Biochemistry, 2002
• Divergent synthesis and biological activities of lipid A analogues of shorter acyl chains
  Tetrahedron, 1998
• Studies on the Asymmetric Synthesis of Stemona Alkaloids: Total Synthesis of (−)‐Stenine
  Angewandte Chemie International Edition in English, 1996
• Efficient reductive etherification of carbonyl compounds with alkoxytrimethylsilanes
  Tetrahedron Letters, 1994
• Synthetic Study of Lipoteichoic Acid of Gram Positive Bacteria. II. Synthesis of the Proposed Fundamental Structure of Enterococcus hirae Lipoteichoic Acid
  Bulletin of the Chemical Society of Japan, 1994
• Synthetic Study on Lipoteichoic Acid of Gram Positive Bacteria. I. Synthesis of Proposed Fundamental Structure of Streptococcus pyogenes Lipoteichoic Acid
  Bulletin of the Chemical Society of Japan, 1992
• 4-Pivaloylaminobenzyl ether, a new temporary protection for hydroxyl functions
  Tetrahedron Letters, 1991
• 4-Nitrobenzyl group for protection of hydroxyl functions
  Tetrahedron Letters, 1990
• General ether synthesis under mild acid-free conditions. Trimethylsilyl iodide catalyzed reductive coupling of carbonyl compounds with trialkylsilanes to symmetrical ethers and reductive condensation with alkoxysilanes to unsymmetrical ethers
  The Journal of Organic Chemistry, 1987