Regioselectivite de la cycloaddition dipolaire-1,3 de munchnones aux alcenes electrophiles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Darstellung und Eigenschaften mesoionischer Oxazolone
2. 1.3‐Dipolare Cycloaddition, LVII. Δ 2 ‐Pyrroline aus N ‐substituierten Oxazolium‐5‐oxiden und olefinischen Dipolarophilen
3. 1,3-Dipolar cycloaddition reactions. LIII. Question of the 1,3-dipolar nature of .DELTA.2-oxazolin-5-ones
4. 1.3‐Dipolare Cycloadditionen, LVI. Eine bequeme Synthese von N ‐substituierten Pyrrolen aus mesoionischen Oxazolonen und Alkinen
5. Synthesis ofN-Substituted Pyrroles From Azlactones via 1,3-Oxazolium 5-Oxides
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3. Synthesis of (5R*)- and (5S*)-5,7,11-trimethyl-3a-phenyl-4,5-dihydro-3aH-1,4-methano[1,3]oxazolo[3,2-a]quinolin-2-ones;Russian Journal of Organic Chemistry;2014-09
4. Modular Mesoionics: Understanding and Controlling Regioselectivity in 1,3-Dipolar Cycloadditions of Münchnone Derivatives;Journal of the American Chemical Society;2013-11-07
5. Phosphonite mediated 1,3-dipolar cycloaddition: a route to polycyclic 2-pyrrolines from imines, acid chlorides and alkenes;Chem. Commun.;2013
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