Relevant bibliographies by topics / Cuparenes

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Cuparenes'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Cuparenes"

1

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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Abad, Antonio, Consuelo Agulló, Manuel Arnó, Ana C. Cuñat, M. Teresa García та Ramón J. Zaragozá. "Enantioselective Synthesis of Cuparane Sesquiterpenes. Synthesis of (−)-Cuparene and (−)-δ-Cuparenol". Journal of Organic Chemistry 61, № 17 (1996): 5916–19. http://dx.doi.org/10.1021/jo960463g.

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3

ABAD, A., C. AGULLO, M. ARNO, A. C. CUNAT, M. T. GARCIA та R. J. ZARAGOZA. "ChemInform Abstract: Enantioselective Synthesis of Cuparane Sesquiterpenes. Synthesis of (-) -Cuparene and (-)-δ-Cuparenol." ChemInform 28, № 6 (2010): no. http://dx.doi.org/10.1002/chin.199706175.

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4

Fuganti, Claudio, and Stefano Serra. "Cuparene Sesquiterpenes: Synthesis of (+)-3-Hydroxycuparene and (+)-Cuparene." Journal of Organic Chemistry 64, no. 23 (1999): 8728–30. http://dx.doi.org/10.1021/jo9909148.

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Fuganti, Claudio, and Stefano Serra. "ChemInform Abstract: Cuparene Sesquiterpenes: Synthesis of (+)-3-Hydroxycuparene and (+)-Cuparene." ChemInform 31, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.200012195.

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6

Ollivier, Jean, Pier Piras, Francesco Secci, and Angelo Frongia. "Convenient Formal Synthesis of (±)-Cuparene, (±)-Enokipodins A and B, and (±)-Cuparene-1,4-Quinone." Synthesis 2007, no. 7 (2007): 999–1002. http://dx.doi.org/10.1055/s-2007-965951.

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7

Srikrishna, A., G. Satyanarayana, and K. R. Prasad. "RCM‐Based Approach to (±)‐Cuparene." Synthetic Communications 37, no. 9 (2007): 1511–16. http://dx.doi.org/10.1080/00397910701229214.

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Ishibashi, Hiroyuki, Taru Su So, Hiroshi Nakatani, Kenjiro Minami, and Masazumi Ikeda. "A short synthesis of (±)-cuparene." J. Chem. Soc., Chem. Commun., no. 12 (1988): 827–28. http://dx.doi.org/10.1039/c39880000827.

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9

Zhao, Xue Zhi, Yan Xing Jia, and Yong Qiang Tu. "An Efficient Synthetic Approach to the Aromatic Sesquiterpenoids via a Smi2-Promoted Construction of Quaternary Centre." Journal of Chemical Research 2003, no. 2 (2003): 54–55. http://dx.doi.org/10.3184/030823403103173101.

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The total synthesis of the natural (±)-cuparene (1) and (±)-herbertene (2) has been carried out in eight steps from 2-cyclohexen-1-one (3) via a key quaternary carbon centre construction using a SmI2-promoted rearrangement of 2,3-epoxy alcohol.
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10

Kladi, Maria, Constantinos Vagias, Giovanni Furnari, Dimitri Moreau, Christos Roussakis, and Vassilios Roussis. "Cytotoxic cuparene sesquiterpenes from Laurencia microcladia." Tetrahedron Letters 46, no. 34 (2005): 5723–26. http://dx.doi.org/10.1016/j.tetlet.2005.06.076.

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Dissertations / Theses on the topic "Cuparenes"

1

Araújo, Ana Lucia Santos de Matos. "Estudos sobre a síntese de microbiotol." Universidade de São Paulo, 1999. http://www.teses.usp.br/teses/disponiveis/59/59132/tde-15102002-163623/.

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Neste trabalho descrevemos vários estudos sintéticos realizados com o objetivo de desenvolver um método para a preparação de Microbiotol (1). A estratégia planejada consistiu em preparar o anel ciclopentano que constitui a metade esquerda da fórmula de (1) acima por contração de anel de isoforona (58), e depois juntar uma cadeia aberta que seria posteriormente ciclizada para formar o segundo anel. A contração do anel da isoforona (58) foi realizada de acordo com as reações a seguir: Os compostos de fórmula geral (85) apresenta considerável congestionamento estérico e resistem fortemente à a
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2

Patel, Aslam. "A photomediated asymmetric synthesis of (-) - cuparene." Thesis, King's College London (University of London), 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.490141.

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3

Patel, Aslam. "Synthetic studies towards a tandem Pummer-Thianazarov cyclisation and a photomediated asymmetric synthesis of cuparene." Thesis, King's College London (University of London), 2005. https://kclpure.kcl.ac.uk/portal/en/theses/synthetic-studies-towards-a-tandem-pummerthianazarov-cyclisation-and-a-photomediated-asymmetric-synthesis-of-cuparene(c06b626f-5e47-46bd-982a-bfbca7b7af5e).html.

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4

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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5

Rao, M. Srinivasa. "Synthesis Of Sesquiterpenes Containing Two Vicinal Quaternary Carbon Atoms." Thesis, 2004. http://hdl.handle.net/2005/333.

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Among nature's creation, terpenoids are more versatile and exciting natural products. In a remarkable display of synthetic ingenuity and creativity, nature has endowed terpenes, more so sesquiterpenes, with a bewildering array of carbocyclic frameworks with unusual assemblage of rings and functionality. This phenomenal structural diversity of this class of natural products makes them ideal targets for developing and testing new synthetic strategies for efficient articulation of carbocyclic frameworks. The present thesis entitled "Synthesis of sesquiterpenes containing two vicinal quaternary ca
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