A new stereoselective synthesis of (±)nootkatone by means of cyclopentenone annulation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Sesquiterpenes. I. Nootkatone, A New Grapefruit Flavor Constituent
2. The constitution of nootkatone, nootkatene and valencene
3. Flavor Studies of Nootkatone in Grapefruit Juice
4. Conversion of Valencene to Nootkatone
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1. One-Pot Synthesis of (+)-Nootkatone via Dark Singlet Oxygenation of Valencene: The Triple Role of the Amphiphilic Molybdate Catalyst;Catalysts;2016-11-26
2. Synthesis, including asymmetric synthesis, of 1-substituted cyclopentenes from cyclobutanones with one-carbon ring-expansion by 1,2-carbon-carbon insertion of magnesium carbenoids;Tetrahedron;2011-02
3. Carbon Elongation of Carbonyl Compounds Utilizing the Rearrangement of Carbenoids-Recent Developments;Journal of Synthetic Organic Chemistry, Japan;2009
4. One-carbon homologation of unsymmetrical ketones through magnesium β-oxido carbenoid rearrangement and trapping the enolate intermediates with electrophiles;Tetrahedron;2008-07
5. One-carbon ring-expansion of 2-substituted cyclohexanones via lithium- and magnesium β-oxido carbenoid rearrangement: a new synthesis of 2,7-disubstituted and 2,2,7-trisubstituted cycloheptanones;Tetrahedron Letters;2006-09
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