L
L. Novak
Researcher at Hungarian Academy of Sciences
Publications - 34
Citations - 81
L. Novak is an academic researcher from Hungarian Academy of Sciences. The author has contributed to research in topics: Sex pheromone & Aryl. The author has an hindex of 5, co-authored 34 publications receiving 81 citations.
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Synthesis and rearrangement of 13-thiaprostanoids
TL;DR: In this article, conjugate addition of mercaptane 6 to cyclopentenones 12 and 20 was interpreted as enolate induced [1,5]-sigmatropic shift on the corresponding dehydration products.
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Baker's yeast mediated synthesis of (5SR, 9S)-5,9-dimethyl-heptadecane and (5SR, 9S)-5,9-dimethyl pentadecane; the main sex-pheromone components of Leucoptera scitella and Perileucoptera coffeella enriched in 9S-isomers
TL;DR: A mixture of (5S, 9S)-5,9-dimethyl heptadecane (1a), the main sex-pheromone component of Leucoptera scitella, and its (5R, 9 S)-isomer (2a) was synthetized conveniently from (R)-citronellal (4, obtained from racemic citronella by enantiomer selective baker's yeast reduction) in four steps as mentioned in this paper.
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Sex pheromone of the cabbage armyworm, mamestra brassicae: isolation, identification and stereocontrolled synthesis
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Novel molecular rearrangements of 4 hydroxy 2 cyclopentenones
TL;DR: In this article, the stereochemistry of the rearrangement is interpreted as the result of synchronous enolate induced [1.5]-sigmatropic rearrangements and stepwise addition-elimination process.
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Rearrangement of Allyl Aryl Ethers I. Reaction of hydroquinone with conjugated Dien-ols and Trien-ol
TL;DR: In this article, a thermal rearrangement of ethers generated in situ from hydroquinone 1 and conjugated polyen-ols 2 afforded 2,3-dihydrobenzofuranols 5, 8 and 10 with 1,3 and/or 3,5 shifts followed by acid catalyzed intramolecular cyclization.