Relevant bibliographies by topics / Diospongin

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books

Academic literature on the topic 'Diospongin'

Author: Grafiati
Published: 4 June 2021
Last updated: 17 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Diospongin.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Diospongin"

1

Bates, Roderick W., and Ping Song. "Synthesis of diospongin A." Tetrahedron 63, no. 21 (2007): 4497–99. http://dx.doi.org/10.1016/j.tet.2007.03.058.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Zúñiga, Andrea, Manuel Pérez, Zoila Gándara, Alioune Fall, Generosa Gómez, and Yagamare Fall. "Synthesis of diospongin A, ent-diospongin A and C-5 epimer of diospongin B from tri-O-acetyl-D-glucal." Arkivoc 2015, no. 7 (2015): 195–215. http://dx.doi.org/10.3998/ark.5550190.p009.191.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Vaithegi, Kannan, and Kavirayani R. Prasad. "Total synthesis of (+)-diospongin A." Tetrahedron 76, no. 47 (2020): 131625. http://dx.doi.org/10.1016/j.tet.2020.131625.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Bharath, Yada, Utkal Mani Choudhury, N. Sadhana, and Debendra K. Mohapatra. "The Mukaiyama type aldol reaction for the synthesis of trans-2,6-disubstituted tetrahydropyrans: synthesis of diospongin A and B." Organic & Biomolecular Chemistry 17, no. 41 (2019): 9169–81. http://dx.doi.org/10.1039/c9ob01549c.

Full text
Abstract:
The synthesis of 2,6-trans-disubstituted tetrahydropyrans following the Mukaiyama type aldol reaction through C–C bond formation demonstrates the practicality of this protocol in the total synthesis of diospongin A and B.
APA, Harvard, Vancouver, ISO, and other styles
5

Chandrasekhar, S., T. Shyamsunder, S. Jaya Prakash, A. Prabhakar, and B. Jagadeesh. "First total synthesis of (−)-diospongin B." Tetrahedron Letters 47, no. 1 (2006): 47–49. http://dx.doi.org/10.1016/j.tetlet.2005.10.129.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Meruva, Suresh Babu, Ramamohan Mekala, Akula Raghunadh, et al. "Synthesis of tetrahedral diarylheptanoid ent-diospongin A and epimer-diospongin B by employing Julia–Kocienski olefination." Tetrahedron Letters 55, no. 34 (2014): 4739–41. http://dx.doi.org/10.1016/j.tetlet.2014.06.112.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Hiebel, Marie-Aude, Béatrice Pelotier, and Olivier Piva. "Total synthesis of (+/−)-diospongin A via Prins reaction." Tetrahedron 63, no. 33 (2007): 7874–78. http://dx.doi.org/10.1016/j.tet.2007.05.089.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Cossy, Janine, Cyril Bressy, and Florent Allais. "A Short and Efficient Synthesis of (-)-Diospongin A." Synlett 2006, no. 20 (2006): 3455–56. http://dx.doi.org/10.1055/s-2006-956485.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Ho, Tse-Lok, Bin Tang, Guohua Ma, and Pengfei Xu. "Concise Synthesis of Yashabushidiol A and (±)-Diospongin A." Journal of the Chinese Chemical Society 59, no. 3 (2012): 455–58. http://dx.doi.org/10.1002/jccs.201100664.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Meruva, Suresh Babu, Ramamohan Mekala, Akula Raghunadh, et al. "ChemInform Abstract: Synthesis of Tetrahedral Diarylheptanoid ent-Diospongin A (I) and epimer-Diospongin B (II) by Employing Julia-Kocienski Olefination." ChemInform 46, no. 5 (2015): no. http://dx.doi.org/10.1002/chin.201505215.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Diospongin"

1

Raffier, Ludovic. "Application de la réaction de métathèse d'oléfines à l'obtention de molécules d'intérêt biologique." Phd thesis, Université Claude Bernard - Lyon I, 2012. http://tel.archives-ouvertes.fr/tel-00986492.

Full text
Abstract:
La formation de liaisons C-C constitue un sujet de recherche primordial en chimie organique. Parmitoutes les techniques existantes, la métathèse d'oléfines a constitué une véritable révolution, notamment grâceau développement de catalyseurs efficaces et tolérants vis-à-vis de bon nombre de groupements fonctionnels.Cette réaction a été envisagée ici sur trois cibles d'intérêt biologique : la diospongine A, la nhatrangine A et leberkeleyamide A.De nombreuses molécules naturelles bioactives appartiennent aux familles des 1,7-diarylheptanoïdes et1,9-diarylnonanoïdes. Issue de la première, la diosp
APA, Harvard, Vancouver, ISO, and other styles
2

Hiebel, Marie-Aude. "Accès stéréocontrôlé aux tétrahydropyranes 2,6-disubstitués – Application à la synthèse totale de la diospongine A et du bistramide A." Lyon 1, 2008. http://www.theses.fr/2008LYO10169.

Full text
Abstract:
L’objectif principal de ce travail est de développer plusieurs voies d’accès à des fragments tétrahydropyranes afin de créer une bibliothèque d’analogues du fragment C1-C13 du bistramide A (partie Nord). L’efficacité et la simplicité de mise en oeuvre des équences réactionnelles sont privilégiées via l’utilisation de procédés tandem séquentiels impliquant la réaction de métathèse croisée. Plusieurs méthodes de formation de cycles tétrahydropyranes se basant respectivement sur les réactions de Prins, d’oxa-Michael, de SN2’ et d’iodoéthérification ont été effectuées. Ces méthodes ont été dans un
APA, Harvard, Vancouver, ISO, and other styles
3

Brito, Júnior Gilmar Araújo. "Estudo metodológico da reação de Prins em ausência de solventes orgânicos e sua aplicação na síntese de substâncias bioativas." Universidade Federal de São Carlos, 2009. https://repositorio.ufscar.br/handle/ufscar/6457.

Full text
Abstract:
Made available in DSpace on 2016-06-02T20:36:24Z (GMT). No. of bitstreams: 1 2736.pdf: 21047421 bytes, checksum: 55df4acf61a3aff2bb08b8ffec4f2fa2 (MD5) Previous issue date: 2009-07-31<br>Financiadora de Estudos e Projetos<br>In this work it was done a methodological study on Prins cyclization reaction in the absence of organic solvents. The synthesis of target compounds was possible by using or the catalytic system pTSA.SiO2(gel) initially developed in this project, as shown in Figure I. As a initial proposal of this work, another catalytics systems were developed, this time using non-proton
APA, Harvard, Vancouver, ISO, and other styles
4

Lee, Kiyoun. "Stereoselective Syntheses of Tetrahydropyrans: Applications to the Synthesis of (+)-Leucascandrolide A, (+)-Dactylolide and (±)-Diospongin A." Diss., 2012. http://hdl.handle.net/10161/6164.

Full text
Abstract:
<p>Substituted tetrahydropyrans are prevalent in natural products that show interesting biological and pharmacological activities. Therefore, demand for new synthetic approaches for the construction of substituted tetrahydropyrans has recently increased. Specifically, quick and facile access to substrates, excellent stereoselectivity and yield, versatility in substrate scope, and mild reaction conditions compatible with various functional groups are highly desirable characteristics in tetrahydropyran synthesis.</p><p>The first part of the dissertation details studies of the tandem and organoca
APA, Harvard, Vancouver, ISO, and other styles

Books on the topic "Diospongin"

1

Lee, Kiyoun. Stereoselective Syntheses of Tetrahydropyrans: Applications to the Synthesis of -Leucascandrolide A, -Dactylolide and -Diospongin A. Springer, 2014.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Diospongin' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography