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Journal articles on the topic 'Marinomycin A'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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1

Bailey, Christopher S., Joseph S. Zarins-Tutt, Matthias Agbo, et al. "A natural solution to photoprotection and isolation of the potent polyene antibiotic, marinomycin A." Chemical Science 10, no. 32 (2019): 7549–53. http://dx.doi.org/10.1039/c9sc01375j.

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Perfect partners for photoprotection: orally ingestible sporopollenin confers striking photoprotection to the powerful, polyene antibiotic, marinomycin A, as well as enabling its selective extraction.
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2

Amans, Dominique, Laurianne Bareille, Véronique Bellosta, and Janine Cossy. "Synthesis of the Monomeric Counterpart of Marinomycin A." Journal of Organic Chemistry 74, no. 20 (2009): 7665–74. http://dx.doi.org/10.1021/jo900945x.

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3

Rajesh, Akkapalli, Gangavaram Sharma, and Krishna Damera. "Stereoselective Synthesis of C13–C28 Fragment of Marinomycin A." Synthesis 47, no. 06 (2014): 845–53. http://dx.doi.org/10.1055/s-0034-1379697.

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4

Nishimaru, Tatsuya, Masashi Kondo, Kimito Takeshita, Keisuke Takahashi, Jun Ishihara, and Susumi Hatakeyama. "Total Synthesis of Marinomycin A Based on a Direct Dimerization Strategy." Angewandte Chemie 126, no. 32 (2014): 8599–602. http://dx.doi.org/10.1002/ange.201404408.

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5

Nishimaru, Tatsuya, Masashi Kondo, Kimito Takeshita, Keisuke Takahashi, Jun Ishihara, and Susumi Hatakeyama. "Total Synthesis of Marinomycin A Based on a Direct Dimerization Strategy." Angewandte Chemie International Edition 53, no. 32 (2014): 8459–62. http://dx.doi.org/10.1002/anie.201404408.

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6

Rajesh, Akkapalli, Gangavaram V. M. Sharma, and Krishna Damera. "ChemInform Abstract: Stereoselective Synthesis of C13-C28 Fragment of Marinomycin A." ChemInform 46, no. 30 (2015): no. http://dx.doi.org/10.1002/chin.201530256.

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7

Amans, Dominique, Véronique Bellosta, and Janine Cossy. "An Efficient and Stereoselective Synthesis of the Monomeric Counterpart of Marinomycin A." Organic Letters 9, no. 8 (2007): 1453–56. http://dx.doi.org/10.1021/ol070240k.

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8

Nishimaru, Tatsuya, Masashi Kondo, Kimito Takeshita, Keisuke Takahashi, Jun Ishihara, and Susumi Hatakeyama. "ChemInform Abstract: Total Synthesis of Marinomycin A Based on a Direct Dimerization Strategy." ChemInform 46, no. 6 (2015): no. http://dx.doi.org/10.1002/chin.201506257.

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9

Evans, P. Andrew, Mu-Hua Huang, Michael J. Lawler, and Sergio Maroto. "Total synthesis of marinomycin A using salicylate as a molecular switch to mediate dimerization." Nature Chemistry 4, no. 8 (2012): 680–84. http://dx.doi.org/10.1038/nchem.1330.

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10

Nicolaou, K. C., Andrea L. Nold, Robert R. Milburn, and Corinna S. Schindler. "Total Synthesis of Marinomycins A–C." Angewandte Chemie International Edition 45, no. 39 (2006): 6527–32. http://dx.doi.org/10.1002/anie.200601867.

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11

Nicolaou, K. C., Andrea L. Nold, Robert R. Milburn, and Corinna S. Schindler. "Total Synthesis of Marinomycins A–C." Angewandte Chemie 118, no. 39 (2006): 6677–82. http://dx.doi.org/10.1002/ange.200601867.

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12

Martis, E. A., G. M. Doshi, G. V. Aggarwal, and P. P. Shanbhag. "Novel Antibiotics from Marine Sources." International Journal of Pharmaceutical Sciences and Nanotechnology 4, no. 3 (2011): 1446–61. http://dx.doi.org/10.37285/ijpsn.2011.4.3.2.

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With the emergence of newer diseases, resistant forms of infectious diseases and multi-drug resistant bacteria, it has become essential to develop novel and more effective antibiotics. Current antibiotics are obtained from terrestrial life or made synthetically from intermediates. The ocean represents virtually untapped resource from which novel antibiotic compounds can be discovered. It is the marine world that will provide the pharmaceutical industry with the next generation of antibiotics. Marine antibiotics are antibiotics obtained from marine organisms. Scientists have reported the discov
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13

Nicolaou, K. C., Andrea L. Nold, Robert R. Milburn, Corinna S. Schindler, Kevin P. Cole, and Junichiro Yamaguchi. "Total Synthesis of Marinomycins A−C and of Their Monomeric Counterparts Monomarinomycin A andiso-Monomarinomycin A." Journal of the American Chemical Society 129, no. 6 (2007): 1760–68. http://dx.doi.org/10.1021/ja068053p.

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14

Kwon, Hak Cheol, Christopher A. Kauffman, Paul R. Jensen, and William Fenical. "Marinomycins A−D, Antitumor-Antibiotics of a New Structure Class from a Marine Actinomycete of the Recently Discovered Genus “Marinispora”." Journal of the American Chemical Society 128, no. 5 (2006): 1622–32. http://dx.doi.org/10.1021/ja0558948.

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15

Kwon, Hak Cheol, Christopher A. Kauffman, Paul R. Jensen, and William Fenical. "Marinomycins A−D, Antitumor-Antibiotics of a New Structure Class from a Marine Actinomycete of the Recently Discovered Genus “Marinispora” [J. Am. Chem. Soc.2006,128, 1622−1632]." Journal of the American Chemical Society 128, no. 50 (2006): 16410. http://dx.doi.org/10.1021/ja0666497.

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16

"Synthesis of Marinomycin A." Synfacts 2007, no. 06 (2007): 0564. http://dx.doi.org/10.1055/s-2007-968513.

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17

"Total Synthesis of (+)-Marinomycin A." Synfacts 8, no. 11 (2012): 1173. http://dx.doi.org/10.1055/s-0032-1317409.

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18

Nicolaou, K. C., Andrea L. Nold, Robert R. Milburn, and Corinna S. Schindler. "Total Synthesis of Marinomycins A—C." ChemInform 38, no. 6 (2007). http://dx.doi.org/10.1002/chin.200706198.

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19

Nicolaou, K. C., Andrea L. Nold, Robert R. Milburn, Corinna S. Schindler, Kevin P. Cole, and Junichiro Yamaguchi. "Total Synthesis of Marinomycins A-C and of Their Monomeric Counterparts Monomarinomycin A and iso-Monomarinomycin A." ChemInform 38, no. 20 (2007). http://dx.doi.org/10.1002/chin.200720195.

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20

Kwon, Hak Cheol, Christopher A. Kauffman, Paul R. Jensen, and William Fenical. "Marinomycins A—D, Antitumor-Antibiotics of a New Structure Class from a Marine Actinomycete of the Recently Discovered Genus “Marinispora”." ChemInform 37, no. 24 (2006). http://dx.doi.org/10.1002/chin.200624214.

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