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Artykuły w czasopismach na temat „(–)-Callystatin A”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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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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2

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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6

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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9

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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10

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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11

Smith III, Amos B., and Benjamin M. Brandt. "ChemInform Abstract: Total Synthesis of (-)-Callystatin A." ChemInform 32, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.200138205.

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12

Dias, Luiz C., and Paulo R. R. Meira. "Synthesis of C1C11 fragment of callystatin A." Tetrahedron Letters 43, no. 49 (2002): 8883–85. http://dx.doi.org/10.1016/s0040-4039(02)02200-1.

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13

Yadav, J. S., K. Yadagiri, Ch Madhuri, and G. Sabitha. "Studies towards the total synthesis of (−)-callystatin A." Tetrahedron Letters 52, no. 33 (2011): 4269–72. http://dx.doi.org/10.1016/j.tetlet.2011.05.151.

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14

Dias, Luiz C., and Paulo R. R. Meira. "Total Synthesis of the Potent Antitumor Polyketide (−)-Callystatin A†." Journal of Organic Chemistry 70, no. 12 (2005): 4762–73. http://dx.doi.org/10.1021/jo050352u.

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15

Raghavan, Sadagopan, and Sheelamanthula Rajendar. "Stereoselective synthesis of the C1–C12 subunit of (−)-callystatin A." Tetrahedron Letters 56, no. 29 (2015): 4371–73. http://dx.doi.org/10.1016/j.tetlet.2015.05.089.

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16

Candy, Mathieu, Loïc Tomas, Sabrina Parat, et al. "A Convergent Approach to (−)-Callystatin A Based on Local Symmetry." Chemistry - A European Journal 18, no. 45 (2012): 14267–71. http://dx.doi.org/10.1002/chem.201202701.

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17

Dias, Luiz C., and Paulo R. R. Meira. "Synthesis of C13C22 fragment of the marine sponge polyketide callystatin A." Tetrahedron Letters 43, no. 2 (2002): 185–87. http://dx.doi.org/10.1016/s0040-4039(01)02104-9.

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18

Kobayashi, Motomasa, Kouichi Higuchi, Nobutoshi Murakami, Hisashi Tajima, and Shunji Aoki. "Callystatin A, a potent cytotoxic polyketide from the marine sponge, Callyspongia truncata." Tetrahedron Letters 38, no. 16 (1997): 2859–62. http://dx.doi.org/10.1016/s0040-4039(97)00482-6.

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19

Vicario, Jose L., Andreas Job, Michael Wolberg, Michael Müller, and Dieter Enders. "Asymmetric Total Synthesis of (−)-Callystatin A Employing the SAMP/RAMP Hydrazone Alkylation Methodology." Organic Letters 4, no. 6 (2002): 1023–26. http://dx.doi.org/10.1021/ol0256116.

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20

Marshall, James A., Ann M. Mikowski, Matthew P. Bourbeau, Gregory M. Schaaf, and Frederick Valeriote. "Leptostatin: A synthetic hybrid of the cytotoxic polyketides callystatin A and leptomycin B." Bioorganic & Medicinal Chemistry Letters 16, no. 2 (2006): 320–23. http://dx.doi.org/10.1016/j.bmcl.2005.09.084.

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21

Reichard, Holly A, Jude C Rieger, and Glenn C Micalizio. "Total Synthesis of Callystatin A by Titanium-Mediated Reductive Alkyne-Alkyne Cross-Coupling." Angewandte Chemie International Edition 47, no. 41 (2008): 7837–40. http://dx.doi.org/10.1002/anie.200803031.

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22

Reichard, Holly A, Jude C Rieger, and Glenn C Micalizio. "Total Synthesis of Callystatin A by Titanium-Mediated Reductive Alkyne-Alkyne Cross-Coupling." Angewandte Chemie 120, no. 41 (2008): 7955–58. http://dx.doi.org/10.1002/ange.200803031.

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23

Dias, Luiz C., and Paulo R. R. Meira. "Corrigendum to “Synthesis of C13–C22 fragment of the marine sponge polyketide callystatin A”." Tetrahedron Letters 43, no. 8 (2002): 1593. http://dx.doi.org/10.1016/s0040-4039(02)00046-1.

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24

Crimmins, Michael T., and Bryan W. King. "Asymmetric Total Synthesis of Callystatin A: Asymmetric Aldol Additions with Titanium Enolates of Acyloxazolidinethiones." Journal of the American Chemical Society 120, no. 35 (1998): 9084–85. http://dx.doi.org/10.1021/ja9817500.

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25

KOBAYASHI, M., K. HIGUCHI, N. MURAKAMI, H. TAJIMA, and S. AOKI. "ChemInform Abstract: Callystatin A, a Potent Cytotoxic Polyketide from the Marine Sponge, Callyspongia truncata." ChemInform 28, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.199731209.

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26

Marshall, James A., and Russell N. Fitzgerald. "Synthesis of asyn,syn,syn,syn-Stereopentad Precursor of the Marine Sponge Polyketide Callystatin A." Journal of Organic Chemistry 64, no. 12 (1999): 4477–81. http://dx.doi.org/10.1021/jo9902143.

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27

Murakami, Nobutoshi, Masanori Sugimoto, Tatsuo Nakajima, Motoyuki Kawanishi, Yasuhiro Tsutsui, and Motomasa Kobayashi. "Participation of the conjugated diene part for potent cytotoxicity of callystatin A, a spongean polyketide." Bioorganic & Medicinal Chemistry 8, no. 11 (2000): 2651–61. http://dx.doi.org/10.1016/s0968-0896(00)00199-1.

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28

Murakami, Nobutoshi, Masanori Sugimoto та Motomasa Kobayashi. "Participation of the β-hydroxyketone part for potent cytotoxicity of callystatin A, a spongean polyketide". Bioorganic & Medicinal Chemistry 9, № 1 (2001): 57–67. http://dx.doi.org/10.1016/s0968-0896(00)00220-0.

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29

Murakami, Nobutoshi, Weiqi Wang, Masashi Aoki, Yasuhiro Tsutsui, Masanori Sugimoto, and Motomasa Kobayashi. "Total synthesis of callystatin A, a potent cytotoxic polyketide from the marine sponge, Callyspongia truncata." Tetrahedron Letters 39, no. 16 (1998): 2349–52. http://dx.doi.org/10.1016/s0040-4039(98)00151-8.

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30

Saeed, Aamer, Babar Hussain Shah, and Rabia Qamar. "A closer look on various synthetic routes to Callystatin A: a cytotoxic marine sponge polyketide." Tetrahedron: Asymmetry 28, no. 9 (2017): 1095–126. http://dx.doi.org/10.1016/j.tetasy.2017.08.015.

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31

Murakami, Nobutoshi, Weiqi Wang, Masashi Aoki, et al. "Absolute stereostructure of callystatin A, a potent cytotoxic polyketide from the marine sponge, Callyspongia truncata." Tetrahedron Letters 38, no. 31 (1997): 5533–36. http://dx.doi.org/10.1016/s0040-4039(97)01194-5.

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32

Dias, Luiz C., and Paulo R. R. Meira. "ChemInform Abstract: Synthesis of C13-C22 Fragment (I) of the Marine Sponge Polyketide Callystatin A." ChemInform 33, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.200214236.

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33

Vicario, Jose L., Andreas Job, Michael Wolberg, Michael Mueller, and Dieter Enders. "ChemInform Abstract: Asymmetric Total Synthesis of (-)-Callystatin A Employing the SAMP/RAMP Hydrazone Alkylation Methodology." ChemInform 33, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.200236220.

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34

Marshall, James A., and Matthew P. Bourbeau. "Second-Generation Synthesis of the Polypropionate Subunit of Callystatin A Based on Regioselective Internal Alkyne Hydrostannation." Organic Letters 4, no. 22 (2002): 3931–34. http://dx.doi.org/10.1021/ol026791m.

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35

CRIMMINS, M. T., and B. W. KING. "ChemInform Abstract: Asymmetric Total Synthesis of Callystatin A: Asymmetric Aldol Additions with Titanium Enolates of Acyloxazolidinethiones." ChemInform 30, no. 3 (2010): no. http://dx.doi.org/10.1002/chin.199903226.

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36

Pujari, Sandip A., and Krishna P. Kaliappan. "An iterative Shimizu non-aldol approach for the stereoselective synthesis of C13-C22 fragment of callystatin A." Organic & Biomolecular Chemistry 10, no. 9 (2012): 1750. http://dx.doi.org/10.1039/c2ob06838a.

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37

MURAKAMI, N., W. WANG, M. AOKI, Y. TSUTSUI, M. SUGIMOTO, and M. KOBAYASHI. "ChemInform Abstract: Total Synthesis of Callystatin A, a Potent Cytotoxic Polyketide from the Marine Sponge, Callyspongia truncata." ChemInform 29, no. 27 (2010): no. http://dx.doi.org/10.1002/chin.199827307.

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38

MURAKAMI, N., W. WANG, M. AOKI, et al. "ChemInform Abstract: Absolute Stereostructure of Callystatin A, a Potent Cytotoxic Polyketide from the Marine Sponge, Callyspongia truncata." ChemInform 28, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199744279.

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39

Marshall, James A., and Russell N. Fitzgerald. "ChemInform Abstract: Synthesis of a syn,syn,syn,syn-Stereopentad Precursor (I) of the Marine Sponge Polyketide Callystatin A." ChemInform 30, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.199938213.

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40

Marshall, James A., and Gregory M. Schaaf. "Synthesis of Stereopentad Analogues of the C14−C22 Segment of Callystatin A through Additions of Chiral Allenylzinc Reagents to Stereotriads." Journal of Organic Chemistry 66, no. 23 (2001): 7825–31. http://dx.doi.org/10.1021/jo015936k.

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41

Marshall, James A., and Gregory M. Schaaf. "ChemInform Abstract: Synthesis of Stereopentad Analogues of the C14-C22 Segment of Callystatin A Through Additions of Chiral Allenylzinc Reagents to Stereotriads." ChemInform 33, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.200218036.

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42

"Synthesis of Callystatin A." Synfacts 2009, no. 04 (2009): 0355. http://dx.doi.org/10.1055/s-0028-1088082.

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43

Langille, Neil F., and James S. Panek. "Total Synthesis of (-)-Callystatin A." ChemInform 35, no. 52 (2004). http://dx.doi.org/10.1002/chin.200452201.

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44

Kurra, Y., G. Sabitha, and Yadav J.S. "Stereoselective Synthesis of C1 -C6 and C7 -C22 Fragments of (-) Callystatin A." October 21, 2015. https://doi.org/10.19070/2332-2756-150001.

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The stereoselective synthesis of the two major fragments (C1 -C6 and C7 -C22) of cytotoxic polyketide marine natural product (-) callystatin A, has been achieved with Sharpless epoxidation, desymmetrization strategy, Horner-Wadsworth-Emmons reaction and witting olefination.

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45

Kalesse, Markus, Khandavalli P. Chary, Monika Quitschalle, Arne Burzlaff, Cornelia Kasper, and Thomas Scheper. "The Total Synthesis of (-)-Callystatin A." ChemInform 34, no. 24 (2003). http://dx.doi.org/10.1002/chin.200324200.

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46

Enders, Dieter, Jose L. Vicario, Andreas Job, Michael Wolberg, and Michael Mueller. "Asymmetric Total Synthesis of (-)-Callystatin A and (-)-20-epi-Callystatin A Employing Chemical and Biological Methods." ChemInform 34, no. 3 (2003). http://dx.doi.org/10.1002/chin.200303212.

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47

Dias, Luiz C., and Paulo R. R. Meira. "Total Synthesis of the Potent Antitumor Polyketide (-)-Callystatin A." ChemInform 36, no. 45 (2005). http://dx.doi.org/10.1002/chin.200545210.

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48

Lautens, Mark, and Timothy Stammers. "Oxabicyclo[3.2.1]oct-6-enes as Templates for the Stereoselective Synthesis of Polypropionates: Total Synthesis of Callystatin A and C19-epi-Callystatin A." Synthesis 2002, no. 14 Special Issue (2002). http://dx.doi.org/10.1055/s-2002-34386.

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49

Lautens, Mark, and Timothy A. Stammers. "Oxabicyclo[3.2.1]oct-6-enes as Templates for the Stereoselective Synthesis of Polypropionates: Total Synthesis of Callystatin A (Ia) and C19-epi-Callystatin A (Ib)." ChemInform 34, no. 7 (2003). http://dx.doi.org/10.1002/chin.200307180.

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50

Y, Kurra, Sabitha G, and Yadav JS. "Stereoselective Synthesis of C1-C6 and C7-C22 Fragments of (-) Callystatin A." International Journal of Bioorganic Chemistry & Molecular Biology, November 21, 2015, 1–11. http://dx.doi.org/10.19070/2332-2756-150001.

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