Relevant bibliographies by topics / Alpha -cuparenone

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Alpha -cuparenone'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Alpha -cuparenone"

1

Taber, Douglass F., Eric H. Petty, and Krishna Raman. "Enantioselective ring construction: synthesis of (+)-.alpha.-cuparenone." Journal of the American Chemical Society 107, no. 1 (1985): 196–99. http://dx.doi.org/10.1021/ja00287a035.

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2

Greene, Andrew E., Florence Charbonnier, Marie Jacqueline Luche, and Albert Moyano. "Enantioselective ring construction through asymmetric olefin-ketene cycloaddition. A highly enantiocontrolled approach to (-)-.alpha.-cuparenone and (+)-.beta.-cuparenone." Journal of the American Chemical Society 109, no. 15 (1987): 4752–53. http://dx.doi.org/10.1021/ja00249a066.

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3

Meyers, A. I., and Bruce A. Lefker. "Chiral bicyclic lactams for asymmetric synthesis of quaternary carbons. The total synthesis of (-)-.alpha.-cuparenone." Journal of Organic Chemistry 51, no. 9 (1986): 1541–44. http://dx.doi.org/10.1021/jo00359a030.

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4

OKANO, KOUJI, HIROSHI SUEMUNE, and KIYOSHI SAKAI. "Formal syntheses of (-)-.ALPHA.- and (+)-.BETA.-cuparenones, cuparene, and laurene." CHEMICAL & PHARMACEUTICAL BULLETIN 36, no. 4 (1988): 1379–85. http://dx.doi.org/10.1248/cpb.36.1379.

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5

Nemoto, Hideo, Hiroki Ishibashi, Masatoshi Nagamochi, and Keiichiro Fukumoto. "A concise and enantioselective approach to cyclobutanones by tandem asymmetric epoxidation and enantiospecific ring expansion of cyclopropylidene alcohols. An enantiocontrolled synthesis of (+)- and (-)-.alpha.-cuparenones." Journal of Organic Chemistry 57, no. 6 (1992): 1707–12. http://dx.doi.org/10.1021/jo00032a021.

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6

Canet, Jean Louis, Antoine Fadel, and Jacques Salaun. "Asymmetric construction of quaternary carbons from chiral malonates: selective and versatile total syntheses of the enantiomers of .alpha.- and .beta.-cuparenones from a common optically active precursor." Journal of Organic Chemistry 57, no. 12 (1992): 3463–73. http://dx.doi.org/10.1021/jo00038a041.

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Dissertations / Theses on the topic "Alpha -cuparenone"

1

Charbonnier, Florence. "Cycloaddition du dichlorocétène avec des éthers d'énols chiraux : application à la synthèse énantiosélective des (-)-[alpha]- et (+)-[bêta]- cuparénones." Grenoble 1, 1987. http://www.theses.fr/1987GRE10069.

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La cycloaddition du dichlorocetene et des ethers d'enols chiraux conduit a des cyclobutanones fonctionnalises avec une diastereoselectivite elevee. Des intermediaires de purete enantiomerique elevee (alpha-chlorocyclopentenones et derives) sont obtenus apres liberation de l'auxiliaire chiral. Dans ce contexte, de nouvelles methodes stereoselectives de preparation d'ethers d'enols chiraux ont ete mises au point. La reduction d'alpha-alcoxy phosphates d'enols issus de l'enolisation stereoselective d'esters a ete appliquee a l'obtention d'ethers d'enols de configuration z. La reduction d'ethers a
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2

CANET, JEAN-LOUIS. "Construction asymetrique de carbones quaternaires a partir de malonates prochiraux : applicatio a la synthese selective des enantiomeres des alpha- et beta-cuparenones et de l'epilaurene. determination des exces enantiomeriques a l'aide de la rmn#2h en milieu cristal liquide cholesterique." Paris 11, 1992. http://www.theses.fr/1992PA112192.

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Le travail rapporte dans ce memoire de these concerne la preparation d'un synthon quaternaire chiral de haute purete enantiomerique et son application a la synthese totale de produits naturels cyclopentaniques. Dans la premiere partie est tout d'abord exposee, par hydrolyse enzymatique enantioselective d'un malonate prochiral, la preparation d'un synthon chiral que nous avons choisi pour conduite selectivement aux enantiomeres des alpha- et beta-cuparenones. Les reductions chimioselectives anormales des fonctions acide et ester de ce chiron, l'acide (r)-(+)-2-methoxycarbonyl-2-(4-methylphenyl)
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