Relevant bibliographies by topics / Lasonolide A

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Lasonolide A'

Author: Grafiati
Published: 4 June 2021
Last updated: 27 July 2025

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Journal articles on the topic "Lasonolide A"

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Wright, Amy E., Ying Chen, Priscilla L. Winder, Tara P. Pitts, Shirley A. Pomponi, and Ross E. Longley. "Lasonolides C−G, Five New Lasonolide Compounds from the SpongeForcepiasp.†." Journal of Natural Products 67, no. 8 (2004): 1351–55. http://dx.doi.org/10.1021/np040028e.

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Lee, Eun, Ho Young Song, Jung Min Joo, et al. "Synthesis of (+)-Lasonolide A: (−)-Lasonolide A is the biologically active enantiomer." Bioorganic & Medicinal Chemistry Letters 12, no. 24 (2002): 3519–20. http://dx.doi.org/10.1016/s0960-894x(02)00821-1.

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Fariña-Ramos, Marta, Celina García, Víctor S. Martín, and Sergio J. Álvarez-Méndez. "Synthetic efforts on the road to marine natural products bearing 4-O-2,3,4,6-tetrasubstituted THPs: an update." RSC Advances 11, no. 10 (2021): 5832–58. http://dx.doi.org/10.1039/d0ra10755g.

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A review covering the synthetic efforts directed to miyakolide, polycavernoside A, lasonolide A, clavosolide A and madeirolide A. They belong to the unique families of marine macrolides bearing 4-O-2,3,4,6 tetrasubstituted THPs.
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Trost, Barry M., Craig E. Stivala, Daniel R. Fandrick, et al. "Total Synthesis of (−)-Lasonolide A." Journal of the American Chemical Society 138, no. 36 (2016): 11690–701. http://dx.doi.org/10.1021/jacs.6b05127.

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Yoshimura, Tomoyuki, Fumika Yakushiji, Shingo Kondo, Xiaofeng Wu, Mitsuru Shindo, and Kozo Shishido. "Total Synthesis of (+)-Lasonolide A." Organic Letters 8, no. 3 (2006): 475–78. http://dx.doi.org/10.1021/ol0527678.

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Clarke, Paul A., Philip B. Sellars, and Nadiah Mad Nasir. "A Maitland–Japp inspired synthesis of dihydropyran-4-ones and their stereoselective conversion to functionalised tetrahydropyran-4-ones." Organic & Biomolecular Chemistry 13, no. 16 (2015): 4743–50. http://dx.doi.org/10.1039/c5ob00292c.

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New variations of the Maitland–Japp reaction have been developed to enable the synthesis of dihydropyrans and tetrahydropyrans with tertiary and quaternary stereocentres, including the functionalised tetrahydropyrans in Civet and the A-ring of lasonolide A.
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Trost, Barry M., Craig E. Stivala, Kami L. Hull, Audris Huang, and Daniel R. Fandrick. "A Concise Synthesis of (−)-Lasonolide A." Journal of the American Chemical Society 136, no. 1 (2013): 88–91. http://dx.doi.org/10.1021/ja411270d.

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8

Kang, Sung Ho, Suk Youn Kang, Chul Min Kim, et al. "Total Synthesis of Natural (+)-Lasonolide A." Angewandte Chemie International Edition 42, no. 39 (2003): 4779–82. http://dx.doi.org/10.1002/anie.200352016.

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Kang, Sung Ho, Suk Youn Kang, Chul Min Kim, et al. "Total Synthesis of Natural (+)-Lasonolide A." Angewandte Chemie 115, no. 39 (2003): 4927–30. http://dx.doi.org/10.1002/ange.200352016.

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Song, Ho Young, Jung Min Joo, Jung Won Kang, et al. "Lasonolide A: Structural Revision and Total Synthesis." Journal of Organic Chemistry 68, no. 21 (2003): 8080–87. http://dx.doi.org/10.1021/jo034930n.

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Dissertations / Theses on the topic "Lasonolide A"

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Milner, Erin Elizabeth Barthelme Crimmins Michael T. "Lasonolide A synthetic explorations /." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2007. http://dc.lib.unc.edu/u?/etd,762.

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Thesis (Ph. D.)--University of North Carolina at Chapel Hill, 2007.<br>Title from electronic title page (viewed Dec. 18, 2007). "... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry." Discipline: Chemistry; Department/School: Chemistry.
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Unch, James Paul. "Studies directed toward the synthesis of the b-Ring of lasonolide A /." The Ohio State University, 2002. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486459267522178.

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Figueroa, Ruth. "Application of the prins cyclization to a synthesis of the tetrahydropyran rings of lasonolide A." Connect to this title online, 2004. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1098890473.

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Thesis (Ph. D.)--Ohio State University, 2004.<br>Title from first page of PDF file. Document formatted into pages; contains xix, 227 p.; also includes graphics. Includes bibliographical references (p. 221-227).
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4

O'Connor, Sean M. J. "Application of Tridentate Schiff Base Chromium (III) Complex Catalysts Towards the Total Synthesis of (-)- Lasonolide A and C-Disaccharide Mimics." Thesis, Griffith University, 2012. http://hdl.handle.net/10072/366217.

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This thesis describes the synthetic studies performed utilizing tridentate Schiff base Cr(III) complex catalysts towards the total synthesis of ()-lasonolide A resulting in the completion of synthetic efforts towards the C17-C25 segment. Further summarization is also given on completion of the C7-C16 segment and an overview of future directions toward to the total synthesis of ()-lasonolide A. Both tetrahydropyrans C7-C11 and C19-C23 were to be constructed utilising an asymmetric hetero-Diels–Alder protocol involving Jacobsen’s hetero-Diels–Alder catalyst providing a means to generate a numb
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Beck, Hartmut. "Asymmetrische Synthese des C1-C16-Segments von Lasonolid A." [S.l. : s.n.], 1998. http://deposit.ddb.de/cgi-bin/dokserv?idn=955899354.

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Beck, Hartmut [Verfasser]. "Asymmetrische Synthese des C1-C16-Segments von Lasonolid A / von Hartmut Beck." 1998. http://d-nb.info/955899354/34.

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Book chapters on the topic "Lasonolide A"

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Taber, Douglass F. "The Trost Synthesis of (−)-Lasonolide A." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0093.

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(−)-Lasonolide A 4, isolated from the Caribbean sponge Forcepia sp., showed remarkable anticancer activity in the NIH 60-cell screen. The central step in the syn­thesis of 4 reported (J. Am. Chem. Soc. 2014, 136, 88) by Barry M. Trost of Stanford University was the remarkably selective, convergent Ru-mediated coupling of 1 with 2 to give 3. To prepare 1, the authors took advantage of the underutilized Cu-mediated addi­tion of a Grignard reagent 6 to propargyl alcohol 5, to give 7. Coupling with the ace­tonide 8 followed by deprotection led to the phosphonium salt 9. The other half of 1 was pre
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"Synthesis of (-)-Blepharocalyxin D, (-)-Lasonolide A, and Attenol A." In Organic Synthesis: State of the 2005-2007. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470385975.ch100.

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Yang, Lin, and Ran Hong. "Integration of novel strategy and methods: total synthesis of antitumor lasonolide A." In Strategies and Tactics in Organic Synthesis. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-814805-1.00004-1.

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"A Recent Example of Structure Determination Through Total Synthesis and Convergent Syntheses: Lasonolide A." In Organic Synthesis via Examination of Selected Natural Products. WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814313711_0012.

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Conference papers on the topic "Lasonolide A"

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Zhang, Yong-Wei, Rozenn Josse, Arun Ghosh, Ji Luo, and Yves Pommier. "Abstract 2117: Lasonolide A-induced premature chromosome condensation is mediated by the proto-oncogene c-Raf (Raf1)." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-2117.

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You might also be interested in the extended bibliographies on the topic 'Lasonolide A' for particular source types:
Journal articles
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