Tandem Claisen rearrangement and ruthenium catalyzed enyne bond reorganization as a route to the synthesis of tricyclic 1,8-naphthyridinones

Authors :: Majumdar, K.C.
Rahaman, H.
Islam, R.
Roy, B.
Source :: Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Mar2006, Vol. 47 Issue 13, p2111-2113. 3p.
Publication Year :: 2006
Abstract: Abstract: A novel procedure for the synthesis of substituted 1,8-naphthyridinones via tandem Claisen rearrangement and ring-closing enyne metathesis is reported. [Copyright &y& Elsevier]

Subjects :: *ETHERS
*CONDENSATION products (Chemistry)
*REARRANGEMENTS (Chemistry)
*CLAISEN rearrangement

Language :: English
ISSN :: 00404039
Volume :: 47
Issue :: 13
Database :: Academic Search Index
Journal :: Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :: Academic Journal
Accession number :: 19841800
Full Text :: https://doi.org/10.1016/j.tetlet.2006.01.132

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