Toward the synthesis of xestocyclamine A: investigation of double Michael reaction and direct aza Diels-Alder reaction Journal Article


Authors: Yun, H.; Gagnon, A.; Danishefsky, S. J.
Article Title: Toward the synthesis of xestocyclamine A: investigation of double Michael reaction and direct aza Diels-Alder reaction
Abstract: An efficient synthesis of the isoquinuclidone core of xestocyclamine A is described. The key step is a direct aza Diels-Alder reaction of enone 14 and p-anisidine to assemble the isoquinuclidone core of xestocyclamine A. © 2006.
Keywords: unclassified drug; drug structure; enzyme inhibitor; drug synthesis; thermodynamics; diels alder reaction; reaction analysis; chemical reaction; stereochemistry; proton nuclear magnetic resonance; cycloaddition; diastereoisomer; annulation reaction; michael addition; anisic acid; quinuclidine derivative; xestocyclamine a; suzuki reaction; betulaceae
Journal Title: Tetrahedron Letters
Volume: 47
Issue: 30
ISSN: 0040-4039
Publisher: Pergamon-Elsevier Science Ltd  
Date Published: 2006-07-24
Start Page: 5311
End Page: 5315
Language: English
DOI: 10.1016/j.tetlet.2006.05.126
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 8" - "Export Date: 4 June 2012" - "CODEN: TELEA" - "Source: Scopus"
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