The β-Methoxyethoxymethyl Protecting Group in Alkaloid Synthesis. Synthesis of Abresoline
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397917808063581
Reference9 articles.
1. Structure of abresoline
2. The acetyl function as a protecting group for phenols
3. Quick, J., Meltz, C. and Ramachandra, R. unpublished results
4. A new general method for protection of the hydroxyl function
5. A New phenylquinolizidol of Heimiasalicifolia
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1. β-Methoxyethoxymethyl chloride (MEMCI);Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15
2. Asymmetric synthesis of (+)-abresoline;Tetrahedron Letters;2005-04
3. Cleavage pattern of alkoxy- or aryloxymethyl ethers induced by mixed hydrides;Tetrahedron Letters;1993-03
4. Prostaglandin F2α photoaffinity probes: 18-phenoxy-19,20-bisnorprostanoids bearing perfluorinated aryl azides;Tetrahedron Letters;1991-03
5. An unexpected difficulty in the use of MEM as a protective group for phenolic hydroxyl;Tetrahedron Letters;1989-01
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