Solvent-Free Carbon–Oxygen Bond Formation Catalysed by CeCl3·7 H2O/NaI: Tetrahydropyranylation of Hydroxy Groups-Reference-Cited by-同舟云学术

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Solvent-Free Carbon–Oxygen Bond Formation Catalysed by CeCl3·7 H2O/NaI: Tetrahydropyranylation of Hydroxy Groups

Published:2006-03 Issue:6 Volume:2006 Page:1476-1482
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Bartoli Giuseppe,Giovannini Riccardo,Giuliani Arianna,Marcantoni Enrico,Massaccesi Massimo,Melchiorre Paolo,Paoletti Melissa,Sambri Letizia

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference73 articles.

1. Protecting groups

2. Fluorous Synthesis: A Fluorous-Phase Strategy for Improving Separation Efficiency in Organic Synthesis

3. Asymmetric Transition Metal-Catalyzed Allylic Alkylations

4. Protecting Groups, 4th ed., Thieme, Stuttgart, 2005 .

5. “Cap-Tag”—Novel Methods for the Rapid Purification of Oligosaccharides Prepared by Automated Solid-Phase Synthesis Financial support from the donors of the Petroleum Research Fund, administered by the ACS (ACS-PRF 34649-G1), Merck (Predoctoral Fellowship for E.R.P.), Boehringer-Ingelheim (Predoctoral Fellowship for E.R.P.), and the NIH (Biotechnology Training Grant for M.C.H.) is gratefully acknowledged. Funding for the MIT-DCIF Inova 501 was provided by the NSF (Award CHE-9808061). Funding for the MIT-DCIF Avance (DPX) 400 was provided by the NIH (Award 1S10RR13886-01). We thank Silicycle (Quebec City, Canada) for the generous gift of fluorous silica gel and isocyanate silica gel scavenger resin. We thank Dr. O. Plante for helpful discussions and help with the automated oligosaccharide synthesizer.

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