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Journal articles on the topic 'Diazonamid'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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1

Roos, Martin. "Diazonamid attackiert Mikrotubuli." Im Focus Onkologie 20, no. 1-2 (2017): 10. http://dx.doi.org/10.1007/s15015-017-3076-6.

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2

Li, Jing, Susan Jeong, Lothar Esser, and Patrick G. Harran. "Total Synthesis of Nominal Diazonamides-Part 1: Convergent Preparation of the Structure Proposed for (−)-Diazonamide A." Angewandte Chemie International Edition 40, no. 24 (2001): 4765–69. http://dx.doi.org/10.1002/1521-3773(20011217)40:24<4765::aid-anie4765>3.0.co;2-1.

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3

Li, Jing, Susan Jeong, Lothar Esser, and Patrick G. Harran. "Total Synthesis of Nominal Diazonamides—Part 1: Convergent Preparation of the Structure Proposed for (−)-Diazonamide A." Angewandte Chemie 113, no. 24 (2001): 4901–6. http://dx.doi.org/10.1002/1521-3757(20011217)113:24<4901::aid-ange4901>3.0.co;2-0.

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4

Li, Jing, Susan Jeong, Lothar Esser, and Patrick G. Harran. "ChemInform Abstract: Total Synthesis of Nominal Diazonamides. Part 1. Convergent Preparation of the Structure Proposed for (-)-Diazonamide A." ChemInform 33, no. 21 (2010): no. http://dx.doi.org/10.1002/chin.200221205.

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5

Nicolaou, K. C., and Jason S. Chen. "Total synthesis of complex heterocyclic natural products." Pure and Applied Chemistry 80, no. 4 (2008): 727–42. http://dx.doi.org/10.1351/pac200880040727.

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Total synthesis campaigns toward complex heterocyclic natural products are a prime source of inspiration for the design and execution of complex cascade sequences, powerful reactions, and efficient synthetic strategies. We highlight selected examples of such innovations in the course of our total syntheses of diazonamide A, azaspiracid-1, thiostrepton, 2,2'-epi-cytoskyrin A and rugulosin, abyssomycin C, platensimycin, and uncialamycin.
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6

Yuen, Alexander K. L., and Craig A. Hutton. "Preparation of Cyclic Peptide Alkaloids Containing Functionalized Tryptophan Residues." Natural Product Communications 1, no. 10 (2006): 1934578X0600101. http://dx.doi.org/10.1177/1934578x0600101010.

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This review covers the synthesis of various cyclic peptide natural products possessing highly functionalized tryptophan residues, focusing on the examples of diazonamide A, the TMC-95 compounds, the celogentin/moroidin family and the complestatin/chloropeptin system. Recent efforts toward the preparation of these modified-tryptophan-containing peptides will be outlined, focusing primarily on the novel methods for the assembly of the highly functionalized indole/tryptophan moieties at the core of these structures.
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7

Knowles, Robert R., Joseph Carpenter, Simon B. Blakey, et al. "Total synthesis of diazonamide A." Chem. Sci. 2, no. 2 (2011): 308–11. http://dx.doi.org/10.1039/c0sc00577k.

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8

Nicolaou, K. C., Marco Bella, David Y. K. Chen, Xianhai Huang, Taotao Ling, and Scott A. Snyder. "Total Synthesis of Diazonamide A." Angewandte Chemie International Edition 41, no. 18 (2002): 3495–99. http://dx.doi.org/10.1002/1521-3773(20020916)41:18<3495::aid-anie3495>3.0.co;2-7.

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9

Li, Jing, Xin Chen, Anthony W. G. Burgett, and Patrick G. Harran. "Synthetic seco Forms of (−)-Diazonamide A." Angewandte Chemie International Edition 40, no. 14 (2001): 2682–85. http://dx.doi.org/10.1002/1521-3773(20010716)40:14<2682::aid-anie2682>3.0.co;2-r.

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10

Li, Jing, Xin Chen, Anthony W. G. Burgett, and Patrick G. Harran. "Synthetic seco Forms of (−)-Diazonamide A." Angewandte Chemie 113, no. 14 (2001): 2754–57. http://dx.doi.org/10.1002/1521-3757(20010716)113:14<2754::aid-ange2754>3.0.co;2-h.

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11

Ritter, Tobias, and Erick M. Carreira. "Die Diazonamide: immer für Überraschungen gut." Angewandte Chemie 114, no. 14 (2002): 2601–6. http://dx.doi.org/10.1002/1521-3757(20020715)114:14<2601::aid-ange2601>3.0.co;2-b.

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12

Bai, Ruoli, Zobeida Cruz-Monserrate, William Fenical, George R. Pettit, and Ernest Hamel. "Interaction of diazonamide A with tubulin." Archives of Biochemistry and Biophysics 680 (February 2020): 108217. http://dx.doi.org/10.1016/j.abb.2019.108217.

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13

Feldman, Ken S., Kyle J. Eastman, and Guillaume Lessene. "Diazonamide Synthesis Studies: Use of Negishi Coupling to Fashion Diazonamide-Related Biaryls with Defined Axial Chirality." Organic Letters 4, no. 20 (2002): 3525–28. http://dx.doi.org/10.1021/ol026694t.

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14

Wittmann, Valentin. "ChemInform Abstract: Synthesis of Putative Diazonamide A." ChemInform 33, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.200229264.

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15

Nicolaou, K. C., Paraselli Bheema Rao, Junliang Hao, et al. "The Second Total Synthesis of Diazonamide A." Angewandte Chemie International Edition 42, no. 15 (2003): 1753–58. http://dx.doi.org/10.1002/anie.200351112.

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16

Ritter, Tobias, and Erick M. Carreira. "The Diazonamides: The Plot Thickens." Angewandte Chemie International Edition 41, no. 14 (2002): 2489–95. http://dx.doi.org/10.1002/1521-3773(20020715)41:14<2489::aid-anie2489>3.0.co;2-v.

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17

Mutule, Ilga, Beomjun Joo, Zane Medne, Toms Kalnins, Edwin Vedejs, and Edgars Suna. "Stereoselective Synthesis of the Diazonamide A Macrocyclic Core." Journal of Organic Chemistry 80, no. 6 (2015): 3058–66. http://dx.doi.org/10.1021/jo5029419.

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18

Vedejs, Edwin, and Jiabing Wang. "A Tyrosine-Derived Benzofuranone Related to Diazonamide A." Organic Letters 2, no. 8 (2000): 1031–32. http://dx.doi.org/10.1021/ol005547x.

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19

Vitkovska, Viktorija, Rimants Zogota, Toms Kalnins, Diana Zelencova, and Edgars Suna. "Aliphatic chain-containing macrocycles as diazonamide A analogs." Chemistry of Heterocyclic Compounds 56, no. 5 (2020): 586–602. http://dx.doi.org/10.1007/s10593-020-02704-6.

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20

Burgett, Anthony W. G., Qingyi Li, Qi Wei, and Patrick G. Harran. "A Concise and Flexible Total Synthesis of (−)-Diazonamide A." Angewandte Chemie 115, no. 40 (2003): 5111–16. http://dx.doi.org/10.1002/ange.200352577.

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21

Burgett, Anthony W. G., Qingyi Li, Qi Wei, and Patrick G. Harran. "A Concise and Flexible Total Synthesis of (−)-Diazonamide A." Angewandte Chemie International Edition 42, no. 40 (2003): 4961–66. http://dx.doi.org/10.1002/anie.200352577.

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22

Ritter, Tobias, and Erick M. Carreira. "ChemInform Abstract: The Diazonamides: The Plot Thickens." ChemInform 33, no. 42 (2010): no. http://dx.doi.org/10.1002/chin.200242254.

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23

Magnus, Philip, and Cyrille Lescop. "Photo-Fries rearrangement for the synthesis of the diazonamide macrocycle." Tetrahedron Letters 42, no. 41 (2001): 7193–96. http://dx.doi.org/10.1016/s0040-4039(01)01515-5.

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24

Zajac, Matthew A., and Edwin Vedejs. "A Synthesis of the Diazonamide Heteroaromatic Biaryl Macrocycle/Hemiaminal Core." Organic Letters 6, no. 2 (2004): 237–40. http://dx.doi.org/10.1021/ol036179a.

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25

Nicolaou, K. C., Scott A Snyder, Klaus B Simonsen, and Alexandros E Koumbis. "Model Studies towards Diazonamide A: Synthesis of the Heterocyclic Core." Angewandte Chemie 39, no. 19 (2000): 3473–78. http://dx.doi.org/10.1002/1521-3773(20001002)39:19<3473::aid-anie3473>3.0.co;2-e.

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26

Vedejs, Edwin, and Jiabing Wang. "ChemInform Abstract: A Tyrosine-Derived Benzofuranone Related to Diazonamide A." ChemInform 31, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.200031202.

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27

David, Nadège, Raffaele Pasceri, Russell R. A. Kitson, Alexandre Pradal, and Christopher J. Moody. "Formal Total Synthesis of Diazonamide A by Indole Oxidative Rearrangement." Chemistry - A European Journal 22, no. 31 (2016): 10867–76. http://dx.doi.org/10.1002/chem.201601605.

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28

Nicolaou, K. C., Scott A Snyder, Klaus B Simonsen, and Alexandros E Koumbis. "Model Studies towards Diazonamide A: Synthesis of the Heterocyclic Core." Angewandte Chemie 112, no. 19 (2000): 3615–20. http://dx.doi.org/10.1002/1521-3757(20001002)112:19<3615::aid-ange3615>3.0.co;2-k.

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29

Moody, C. J., K. J. Doyle, M. C. Elliott, and T. J. Mowlem. "Synthesis of heterocyclic natural products: Model studies towards diazonamide A." Pure and Applied Chemistry 66, no. 10-11 (1994): 2107–10. http://dx.doi.org/10.1351/pac199466102107.

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30

Wipf, Peter, and Fumiaki Yokokawa. "Synthetic studies toward diazonamide A. Preparation of the benzofuranone-indolyloxazole fragment." Tetrahedron Letters 39, no. 16 (1998): 2223–26. http://dx.doi.org/10.1016/s0040-4039(98)00231-7.

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31

Magnus, Philip, and Jennifer D. Kreisberg. "Synthesis of benzofuranones related to diazonamide via an intramolecular Pummerer reaction." Tetrahedron Letters 40, no. 3 (1999): 451–54. http://dx.doi.org/10.1016/s0040-4039(98)02386-7.

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32

Jeong, Susan, Xin Chen, and Patrick G. Harran. "Macrocyclic Triarylethylenes via Heck Endocyclization: A System Relevant to Diazonamide Synthesis." Journal of Organic Chemistry 63, no. 24 (1998): 8640–41. http://dx.doi.org/10.1021/jo981791e.

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33

Ding, Hui, Patrick L. DeRoy, Christian Perreault, et al. "Electrolytic Macrocyclizations: Scalable Synthesis of a Diazonamide-Based Drug Development Candidate." Angewandte Chemie 127, no. 16 (2015): 4900–4904. http://dx.doi.org/10.1002/ange.201411663.

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34

Ding, Hui, Patrick L. DeRoy, Christian Perreault, et al. "Electrolytic Macrocyclizations: Scalable Synthesis of a Diazonamide-Based Drug Development Candidate." Angewandte Chemie International Edition 54, no. 16 (2015): 4818–22. http://dx.doi.org/10.1002/anie.201411663.

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35

Wipf, Peter, and Joey-Lee Methot. "Synthetic Studies toward Diazonamide A. A Novel Approach for Polyoxazole Synthesis." Organic Letters 3, no. 9 (2001): 1261–64. http://dx.doi.org/10.1021/ol0157196.

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36

Mutule, Ilga, Toms Kalnins, Edwin Vedejs, and Edgars Suna. "Diazonamide synthetic studies. Reactivity of N-unsubstituted benzofuro[2,3-b]indolines." Chemistry of Heterocyclic Compounds 51, no. 7 (2015): 613–20. http://dx.doi.org/10.1007/s10593-015-1749-7.

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37

Magnus, Philip, and Rachel Turnbull. "Methodology for the synthesis of the core EFGH rings of diazonamide A." Tetrahedron Letters 47, no. 36 (2006): 6461–64. http://dx.doi.org/10.1016/j.tetlet.2006.06.123.

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38

Palmer, Francine N., Franck Lach, Cyril Poriel, et al. "The diazo route to diazonamide A: studies on the tyrosine-derived fragment." Organic & Biomolecular Chemistry 3, no. 20 (2005): 3805. http://dx.doi.org/10.1039/b510653b.

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39

Magnus, Philip, Jennifer D. Venable (nee Kreisberg), Lan Shen, and Vince Lynch. "Some reactions of persistent benzofuranone radicals related to the ‘old’ diazonamide structure." Tetrahedron Letters 46, no. 4 (2005): 707–10. http://dx.doi.org/10.1016/j.tetlet.2004.11.103.

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40

Nicolaou, K. C., Junliang Hao, Mali V. Reddy, et al. "Chemistry and Biology of Diazonamide A: Second Total Synthesis and Biological Investigations." Journal of the American Chemical Society 126, no. 40 (2004): 12897–906. http://dx.doi.org/10.1021/ja040093a.

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41

Chen, Xin, Lothar Esser, and Patrick G. Harran. "Stereocontrol in Pinacol Ring-Contraction of Cyclopeptidyl Glycols: The Diazonamide C10 Problem." Angewandte Chemie International Edition 39, no. 5 (2000): 937–40. http://dx.doi.org/10.1002/(sici)1521-3773(20000303)39:5<937::aid-anie937>3.0.co;2-a.

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42

MOODY, C. J., K. J. DOYLE, M. C. ELLIOTT, and T. J. MOWLEM. "ChemInform Abstract: Synthesis of Heterocyclic Natural Products: Model Studies Towards Diazonamide A." ChemInform 26, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199507302.

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43

Chen, Xin, Lothar Esser, and Patrick G. Harran. "Stereocontrol in Pinacol Ring-Contraction of Cyclopeptidyl Glycols: The Diazonamide C10 Problem." Angewandte Chemie 112, no. 5 (2000): 967–70. http://dx.doi.org/10.1002/(sici)1521-3757(20000303)112:5<967::aid-ange967>3.0.co;2-m.

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44

Magnus, Philip, and Cyrille Lescop. "ChemInform Abstract: Photo-Fries Rearrangement for the Synthesis of the Diazonamide Macrocycle." ChemInform 33, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.200202233.

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45

Vedejs, Edwin, and Matthew A. Zajac. "Synthesis of the Diazonamide A Macrocyclic Core via a Dieckmann-Type Cyclization." Organic Letters 3, no. 16 (2001): 2451–54. http://dx.doi.org/10.1021/ol016097r.

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46

Zhang, Jianmin, and Marco A. Ciufolini. "An Approach to the Bis-oxazole Macrocycle of Diazonamides." Organic Letters 13, no. 3 (2011): 390–93. http://dx.doi.org/10.1021/ol102678j.

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47

Lach, Franck, and Christopher J. Moody. "Studies towards the synthesis of diazonamide A. Synthesis of a tyrosine-derived benzofuranone." Tetrahedron Letters 41, no. 35 (2000): 6893–96. http://dx.doi.org/10.1016/s0040-4039(00)01118-7.

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48

Nicolaou, K. C., Scott A. Snyder, Xianhai Huang, Klaus B. Simonsen, Alexandros E. Koumbis, and Antony Bigot. "Studies toward Diazonamide A: Initial Synthetic Forays Directed toward the Originally Proposed Structure." Journal of the American Chemical Society 126, no. 32 (2004): 10162–73. http://dx.doi.org/10.1021/ja040090y.

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49

Magnus, Philip, and Jennifer D. Kreisberg. "ChemInform Abstract: Synthesis of Benzofuranones Related to Diazonamide via an Intramolecular Pummerer Reaction." ChemInform 30, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.199917119.

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50

WIPF, P., and F. YOKOKAWA. "ChemInform Abstract: Synthetic Studies Toward Diazonamide A. Preparation of the Benzofuranone-Indolyloxazole Fragment." ChemInform 29, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199829294.

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