72453-37-3Relevant academic research and scientific papers
An efficient and economic asymmetric synthesis of (+)-nootkatone, tetrahydronootkatone, and derivatives
Sauer, Anne M.,Crowe, William E.,Henderson, Gregg,Laine, Roger A.
, p. 3530 - 3533 (2009)
Image Persented A facile route to enantiomerically pure (+)-nootkatone and derivatives has been established through conjunctive stereoselective Grignard/anionic oxy-Cope (AOC) reactions.
REACTION SEQUENCE FOR THE SYNTHESIS OF NOOTKATONE, DIHYDRONOOTKATONE, AND TETRAHYDRONOOTKATONE
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Paragraph 00017; 00018, (2017/07/06)
An inexpensive, stereoselective synthesis for nootkatone, tetrahydronootkatone, and their derivatives is disclosed utilizing ozonolysis. The starting materials used in the synthesis are inexpensive and the reactions are commercially feasible and amenable to scaling up. The principal starting material, (?)-β-Pinene, is on the GRAS list (generally recognized as safe).
Efficient and economic asymmetric synthesis of nootkatone, tetrahydronootkatone, their precursors and derivatives
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Page/Page column 3, (2010/11/23)
An inexpensive, stereoselective synthesis for nootkatone, tetrahydronootkatone, and their derivatives is disclosed. The starting materials used in the synthesis are inexpensive. The principal starting material, (?)-β-Pinene, is on the GRAS list (generally recognized as safe).
Synthetic Study of (+)-Nootkatone from (-)-β-Pinene
Yanami, Tetsuji,Miyashita, Masaaki,Yoshikoshi, Akira
, p. 607 - 612 (2007/10/02)
A facile stereoselective synthesis of (+)-nootkatone (1) has been achieved starting with (+)-nopinone (2b).The key step was the conjugate addition of methallyltrimethylsilane (20b) to trans-3-ethylidenenopinone (16), which was obtainable from 2b on the cross condensation with acetaldehyde followed by acid treatment, giving an adduct with the desired stereochemistry, 24a, as the predominant product.Dione 23, obtained from the adduct on methylation followed by ozonization, afforded nootkatone hydrochloride (26) on treatment with hydrogen chloride.Regioselective dehydrochlorination of the hydrochloride yielded 1.An alternative route in which allyltrimethylsilane was used is also described.
