Novel Synthesis of Protected Methyl 4-Hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylate via Cleavage of Functionalized Dihydrooxazoles (Oxazolines)
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1999/JC/A807330I
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1. A comparison of the cardiovascular actions of AQ 110 with those of isoprenaline and salbutamol
2. XXXI.—A synthesis of hydrastine. Part I
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1. ChemInform Abstract: Novel Synthesis of Protected Methyl 4-Hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylate via Cleavage of Functionalized Dihydrooxazoles (Oxazolines).;ChemInform;2010-06-15
2. Microwave-assisted solvent-free heterocyclic synthesis;Journal of Photochemistry and Photobiology C: Photochemistry Reviews;2005-10
3. Microwave Irradiation for Accelerating Organic Reactions. Part I: Three-, Four- and Five-Membered Heterocycles;Advances in Heterocyclic Chemistry;2005
4. Microwave assisted organic synthesis—a review;Tetrahedron;2001-11
5. A practical ‘one-pot’ synthesis of ethyl isoquinoline-3-carboxylate by domino reactions: a potential entry to constrained nonproteogenic amino acid derivatives;Tetrahedron Letters;2001-02
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