Relevant bibliographies by topics / Auripyrone / Journal articles

Journal articles on the topic 'Auripyrone'

To see the other types of publications on this topic, follow the link: Auripyrone.
Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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

Select a source type:

Consult the top 18 journal articles for your research on the topic 'Auripyrone.'

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.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Lister, Troy, and Michael V. Perkins. "Total Synthesis of Auripyrone A." Angewandte Chemie International Edition 45, no. 16 (April 10, 2006): 2560–64. http://dx.doi.org/10.1002/anie.200504573.

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

Lister, Troy, and Michael V. Perkins. "Total Synthesis of Auripyrone A." Angewandte Chemie 118, no. 16 (April 10, 2006): 2622–26. http://dx.doi.org/10.1002/ange.200504573.

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

Hayakawa, Ichiro, Takuma Takemura, Emi Fukasawa, Yuta Ebihara, Natsuki Sato, Takayasu Nakamura, Kiyotake Suenaga, and Hideo Kigoshi. "Total Synthesis of Auripyrones A and B and Determination of the Absolute Configuration of Auripyrone B." Angewandte Chemie International Edition 49, no. 13 (February 23, 2010): 2401–5. http://dx.doi.org/10.1002/anie.200906662.

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

Hayakawa, Ichiro, Takuma Takemura, Emi Fukasawa, Yuta Ebihara, Natsuki Sato, Takayasu Nakamura, Kiyotake Suenaga, and Hideo Kigoshi. "Total Synthesis of Auripyrones A and B and Determination of the Absolute Configuration of Auripyrone B." Angewandte Chemie 122, no. 13 (February 23, 2010): 2451–55. http://dx.doi.org/10.1002/ange.200906662.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Perkins, Michael V., Saba Jahangiri, and Max R. Taylor. "Stereoselective synthesis of a novel spiroacetal-dihydropyrone related to auripyrone." Tetrahedron Letters 47, no. 12 (March 2006): 2025–28. http://dx.doi.org/10.1016/j.tetlet.2006.01.045.

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

Jung, Michael E., and Ramin Salehi-Rad. "Dipyrone approach toward the synthesis of the cytotoxic natural product auripyrone A." Tetrahedron Letters 51, no. 38 (September 2010): 4931–33. http://dx.doi.org/10.1016/j.tetlet.2010.07.034.

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

Perkins, Michael V., Rebecca A. Sampson, John Joannou, and Max R. Taylor. "Stereoselective synthesis and cyclisation of the acyclic precursor to auripyrone A and B." Tetrahedron Letters 47, no. 22 (May 2006): 3791–95. http://dx.doi.org/10.1016/j.tetlet.2006.03.096.

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

Jung, Michael E., Manon Chaumontet, and Ramin Salehi-Rad. "Total Synthesis of Auripyrone B Using a Non-Aldol Aldol−Cuprate Opening Process." Organic Letters 12, no. 12 (June 18, 2010): 2872–75. http://dx.doi.org/10.1021/ol100985n.

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

Jung, Michael E., Manon Chaumontet, and Ramin Salehi-Rad. "ChemInform Abstract: Total Synthesis of Auripyrone B Using a Non-Aldol Aldol-Cuprate Opening Process." ChemInform 41, no. 44 (October 7, 2010): no. http://dx.doi.org/10.1002/chin.201044210.

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

Jung, Michael E, and Ramin Salehi-Rad. "Total Synthesis of Auripyrone A Using a Tandem Non-Aldol Aldol/Paterson Aldol Process as a Key Step." Angewandte Chemie International Edition 48, no. 46 (November 2, 2009): 8766–69. http://dx.doi.org/10.1002/anie.200904607.

Full text
APA, Harvard, Vancouver, ISO, and other styles
11

Jung, Michael E, and Ramin Salehi-Rad. "Total Synthesis of Auripyrone A Using a Tandem Non-Aldol Aldol/Paterson Aldol Process as a Key Step." Angewandte Chemie 121, no. 46 (November 2, 2009): 8922–25. http://dx.doi.org/10.1002/ange.200904607.

Full text
APA, Harvard, Vancouver, ISO, and other styles
12

Hayakawa, Ichiro, Takuma Takemura, Emi Fukasawa, Yuta Ebihara, Natsuki Sato, Takayasu Nakamura, Kiyotake Suenaga, and Hideo Kigoshi. "Total Synthesis and Biological Evaluation of Auripyrones A and B." Bulletin of the Chemical Society of Japan 85, no. 10 (October 15, 2012): 1077–92. http://dx.doi.org/10.1246/bcsj.20120162.

Full text
APA, Harvard, Vancouver, ISO, and other styles
13

Hayakawa, Ichiro, Takuma Takemura, Emi Fukasawa, Yuta Ebihara, Natsuki Sato, Takayasu Nakamura, Kiyotake Suenaga, and Hideo Kigoshi. "ChemInform Abstract: Total Synthesis and Biological Evaluation of Auripyrones A and B." ChemInform 44, no. 8 (February 19, 2013): no. http://dx.doi.org/10.1002/chin.201308178.

Full text
APA, Harvard, Vancouver, ISO, and other styles
14

Suenaga, Kiyotake, Hideo Kigoshi, and Kiyoyuki Yamada. "Auripyrones A and B, cytotoxic polypropionates from the sea hare Dolabella auricularia: Isolation and structures." Tetrahedron Letters 37, no. 29 (July 1996): 5151–54. http://dx.doi.org/10.1016/0040-4039(96)01041-6.

Full text
APA, Harvard, Vancouver, ISO, and other styles
15

SUENAGA, K., H. KIGOSHI, and K. YAMADA. "ChemInform Abstract: Auripyrones A and B, Cytotoxic Polypropionates from the Sea Hare Dolabella auricularia: Isolation and Structures." ChemInform 27, no. 43 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199643226.

Full text
APA, Harvard, Vancouver, ISO, and other styles
16

Singh, Keisham S. "Pyrone-derived Marine Natural Products: A Review on Isolation, Bio-activities and Synthesis." Current Organic Chemistry 24, no. 4 (May 9, 2020): 354–401. http://dx.doi.org/10.2174/1385272824666200217101400.

Full text
Abstract:
Marine natural products (MNPs) containing pyrone rings have been isolated from numerous marine organisms, and also produced by marine fungi and bacteria, particularly, actinomycetes. They constitute a versatile structure unit of bioactive natural products that exhibit various biological activities such as antibiotic, antifungal, cytotoxic, neurotoxic, phytotoxic and anti-tyrosinase. The two structure isomers of pyrone ring are γ- pyrone and α-pyrone. In terms of chemical motif, γ-pyrone is the vinologous form of α- pyrone which possesses a lactone ring. Actinomycete bacteria are responsible for the production of several α-pyrone compounds such as elijopyrones A-D, salinipyrones and violapyrones etc. to name a few. A class of pyrone metabolites, polypropionates which have fascinating carbon skeleton, is primarily produced by marine molluscs. Interestingly, some of the pyrone polytketides which are found in cone snails are actually synthesized by actinomycete bacteria. Several pyrone derivatives have been obtained from marine fungi such as Aspergillums flavus, Altenaria sp., etc. The γ-pyrone derivative namely, kojic acid obtained from Aspergillus fungus has high commercial demand and finds various applications. Kojic acid and its derivative displayed inhibition of tyrosinase activity and, it is also extensively used as a ligand in coordination chemistry. Owing to their commercial and biological significance, the synthesis of pyrone containing compounds has been given attention over the past years. Few reviews on the total synthesis of pyrone containing natural products namely, polypropionate metabolites have been reported. However, these reviews skipped other marine pyrone metabolites and also omitted discussion on isolation and detailed biological activities. This review presents a brief account of the isolation of marine metabolites containing a pyrone ring and their reported bio-activities. Further, the review covers the synthesis of marine pyrone metabolites such as cyercene-A, placidenes, onchitriol-I, onchitriol-II, crispatene, photodeoxytrichidione, (-) membrenone-C, lihualide-B, macrocyclic enol ethers and auripyrones-A & B.
APA, Harvard, Vancouver, ISO, and other styles
17

Lister, Troy, and Michael V. Perkins. "Total Synthesis of Auripyrone A." ChemInform 37, no. 33 (August 15, 2006). http://dx.doi.org/10.1002/chin.200633240.

Full text
APA, Harvard, Vancouver, ISO, and other styles
18

"Synthesis of Auripyrones A and B." Synfacts 2010, no. 07 (June 22, 2010): 0738. http://dx.doi.org/10.1055/s-0029-1220107.

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