Relevant bibliographies by topics / (–)-Callystatin A

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

Academic literature on the topic '(–)-Callystatin A'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "(–)-Callystatin A"

1

Raghavan, Sadagopan, and Sheelamanthula Rajendar. "Stereoselective synthesis of the C13–C22 fragment of callystatin A by a non-aldol approach." Organic & Biomolecular Chemistry 13, no. 17 (2015): 5044–53. http://dx.doi.org/10.1039/c5ob00413f.

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Dias, Luiz C., Luciana G. de Oliveira, and Paulo R. R. Meira. "Recent results toward the stereoselective synthesis of biologically active natural products." Pure and Applied Chemistry 79, no. 2 (2007): 163–72. http://dx.doi.org/10.1351/pac200779020163.

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This paper describes the convergent and stereocontrolled asymmetric total synthesis of (+)-crocacins C and D, potent inhibitors of animal cell cultures and several yeasts and fungi, and (-)-callystatin A, a potent antitumor polyketide.
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3

Langille, Neil F., and James S. Panek. "Total Synthesis of (−)-Callystatin A." Organic Letters 6, no. 18 (2004): 3203–6. http://dx.doi.org/10.1021/ol048664r.

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4

Marshall, James A., and Matthew P. Bourbeau. "Total Synthesis of (−)-Callystatin A." Journal of Organic Chemistry 67, no. 9 (2002): 2751–54. http://dx.doi.org/10.1021/jo016025d.

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5

Smith, Amos B., and Benjamin M. Brandt. "Total Synthesis of (−)-Callystatin A." Organic Letters 3, no. 11 (2001): 1685–88. http://dx.doi.org/10.1021/ol0158922.

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Kalesse, Markus, Monika Quitschalle, Chary P. Khandavalli, and Aamer Saeed. "Total Synthesis of (−)-Callystatin A." Organic Letters 3, no. 20 (2001): 3107–9. http://dx.doi.org/10.1021/ol016365l.

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7

Kalesse, Markus, Khandavalli P. Chary, Monika Quitschalle, Arne Burzlaff, Cornelia Kasper, and Thomas Scheper. "The Total Synthesis of (−)-Callystatin A." Chemistry - A European Journal 9, no. 5 (2003): 1129–36. http://dx.doi.org/10.1002/chem.200390130.

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8

Enders, Dieter, Jose L. Vicario, Andreas Job, Michael Wolberg, and Michael Müller. "Asymmetric Total Synthesis of (−)-Callystatin A and (−)-20-epi-Callystatin A Employing Chemical and Biological Methods." Chemistry - A European Journal 8, no. 18 (2002): 4272–84. http://dx.doi.org/10.1002/1521-3765(20020916)8:18<4272::aid-chem4272>3.0.co;2-k.

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Kalesse, Markus, Monika Quitschalle, Chary P. Khandavalli, and Aamer Saeed. "ChemInform Abstract: Total Synthesis of (-)-Callystatin A." ChemInform 33, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.200205218.

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Marshall, James A., and Matthew P. Bourbeau. "ChemInform Abstract: Total Synthesis of (-)-Callystatin A." ChemInform 33, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.200251212.

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Dissertations / Theses on the topic "(–)-Callystatin A"

1

Wildman, Tanya. "Studies on 1,2 metallate rearrangements : application to Callystatin A." Thesis, University of Leeds, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275804.

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Parat, Sabrina. "Approche synthétique d’une delta-lactone alpha, beta-insaturée naturelle bioactive, la (–)-Callystatine A." Aix-Marseille 3, 2008. http://www.theses.fr/2008AIX30016.

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Abstract:
La (–)-Callystatine A est un produit naturel bioactif d’origine marine. Son activité biologique et sa structure complexe, qui font de cette molécule une cible synthétique de choix, ont suscité notre intérêt. Le mémoire débute par une partie bibliographique consacrée à l’examen des neuf synthèses totales de la Callystatine A, suivie de l’application de la désymétrisation énantiosélective des composés méso en synthèse totale. Notre stratégie repose sur la synthèse originale de trois fragments. La chaîne polypropionate du fragment Ouest est synthétisée via la désymétrisation d’un diol méso et une
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3

Bourbeau, Matthew Paul. "The total synthesis of (-)-callystatin A and related studies /." 2003. http://wwwlib.umi.com/dissertations/fullcit/3097286.

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Books on the topic "(–)-Callystatin A"

1

Stammers, Timothy. Total synthesis of Callystatin A and C-9-epi-Callystatin A. 2002.

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Journal articles
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