Log in

Relevant bibliographies by topics / Neopeltolide / Journal articles

To see the other types of publications on this topic, follow the link: Neopeltolide.

Journal articles on the topic 'Neopeltolide'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Neopeltolide.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Scheidt, K., D. Custar, and T. Zabawa. "Synthesis of Neopeltolide." Synfacts 2008, no. 7 (July 2008): 0677. http://dx.doi.org/10.1055/s-2008-1077862.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Fuwa, Haruhiko, Shinya Naito, Tomomi Goto, and Makoto Sasaki. "Total Synthesis of (+)-Neopeltolide." Angewandte Chemie 120, no. 25 (June 9, 2008): 4815–17. http://dx.doi.org/10.1002/ange.200801399.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Fuwa, Haruhiko, Shinya Naito, Tomomi Goto, and Makoto Sasaki. "Total Synthesis of (+)-Neopeltolide." Angewandte Chemie International Edition 47, no. 25 (June 9, 2008): 4737–39. http://dx.doi.org/10.1002/anie.200801399.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Yanagi, Shota, Tomoya Sugai, Takuma Noguchi, Masato Kawakami, Makoto Sasaki, Shinsuke Niwa, Asako Sugimoto, and Haruhiko Fuwa. "Fluorescence-labeled neopeltolide derivatives for subcellular localization imaging." Organic & Biomolecular Chemistry 17, no. 28 (2019): 6771–76. http://dx.doi.org/10.1039/c9ob01276a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Larsen, Erik M., Chia-Fu Chang, Tomoyo Sakata-Kato, Joseph W. Arico, Vince M. Lombardo, Dyann F. Wirth, and Richard E. Taylor. "Conformation-guided analogue design identifies potential antimalarial compounds through inhibition of mitochondrial respiration." Organic & Biomolecular Chemistry 16, no. 30 (2018): 5403–6. http://dx.doi.org/10.1039/c8ob01257a.

Full text

Abstract:

The design, synthesis, conformational analysis, and biological evaluation of 2-methyl neopeltolide has been accomplished and shown to possess mitochondrial respiration inhibitory activity in malarial parasites.

APA, Harvard, Vancouver, ISO, and other styles

6

Athe, Sudhakar, Balla Chandrasekhar, Saumya Roy, Tapan Kumar Pradhan, and Subhash Ghosh. "Formal Total Synthesis of (+)-Neopeltolide." Journal of Organic Chemistry 77, no. 21 (October 15, 2012): 9840–45. http://dx.doi.org/10.1021/jo301425c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Vintonyak, Viktor V., and Martin E. Maier. "Formal Total Synthesis of Neopeltolide." Organic Letters 10, no. 6 (March 2008): 1239–42. http://dx.doi.org/10.1021/ol8001255.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Yang, Zhen, Bingbin Zhang, Gaoyuan Zhao, Juan Yang, Xingang Xie, and Xuegong She. "Concise Formal Synthesis of (+)-Neopeltolide." Organic Letters 13, no. 21 (November 4, 2011): 5916–19. http://dx.doi.org/10.1021/ol2025718.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Masiuk, Uladzimir S., Iryna V. Mineyeva, and Dzmitry G. Kananovich. "Highly Diastereoselective Chelation-Controlled 1,3-anti-Allylation of (S)-3-(Methoxymethyl)hexanal Enabled by Hydrate of Scandium Triflate." Symmetry 13, no. 3 (March 13, 2021): 470. http://dx.doi.org/10.3390/sym13030470.

Full text

Abstract:

En route to the total synthesis of (+)-Neopeltolide, we explored Lewis acid-assisted diastereoselective allylation of MOM-protected 3-hydroxylhexanal with β-(2,2-diethoxyethyl)-substituted (allyl)tributylstannane. The hydrated form of scandium triflate was found to be essential for attaining high 1,3-anti-diastereoselectivity (d.r. 94:6), while the use of anhydrous catalyst resulted in a modest diastereocontrol (d.r. 76:24). The preferred 1,3-anti-selectivity in this transformation can be rationalized in the framework of the Reetz chelate model of asymmetric induction. The 1,3-anti-configuration of the product was confirmed by its conversion into the known C7-C16 building block of (+)-Neopeltolide. We also report an improved protocol for the synthesis of β-(2,2-diethoxyethyl)-substituted (allyl)tributylstannane, which can be utilized as a cost-efficient bipolar isoprenoid-type C5-building block in the synthesis of natural compounds.

APA, Harvard, Vancouver, ISO, and other styles

10

Cui, Yubo, Wangyang Tu, and Paul E. Floreancig. "Total synthesis of neopeltolide and analogs." Tetrahedron 66, no. 26 (June 2010): 4867–73. http://dx.doi.org/10.1016/j.tet.2010.03.066.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Fuwa, Haruhiko, Asami Saito, and Makoto Sasaki. "A Concise Total Synthesis of (+)-Neopeltolide." Angewandte Chemie 122, no. 17 (March 22, 2010): 3105–8. http://dx.doi.org/10.1002/ange.201000624.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Fuwa, Haruhiko, Asami Saito, and Makoto Sasaki. "A Concise Total Synthesis of (+)-Neopeltolide." Angewandte Chemie International Edition 49, no. 17 (March 22, 2010): 3041–44. http://dx.doi.org/10.1002/anie.201000624.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Ghosh, Arun K., Khriesto A. Shurrush, and Zachary L. Dawson. "Enantioselective total synthesis of macrolide (+)-neopeltolide." Organic & Biomolecular Chemistry 11, no. 44 (2013): 7768. http://dx.doi.org/10.1039/c3ob41541d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Gallon, Julien, Sébastien Reymond, and Janine Cossy. "Neopeltolide, a new promising antitumoral agent." Comptes Rendus Chimie 11, no. 11-12 (November 2008): 1463–76. http://dx.doi.org/10.1016/j.crci.2008.08.006.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Guinchard, Xavier, and Emmanuel Roulland. "Total Synthesis of the Antiproliferative Macrolide (+)-Neopeltolide." Organic Letters 11, no. 20 (October 15, 2009): 4700–4703. http://dx.doi.org/10.1021/ol902047z.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Youngsaye, Willmen, Jason T Lowe, Frauke Pohlki, Paul Ralifo, and James S Panek. "Total Synthesis and Stereochemical Reassignment of (+)-Neopeltolide." Angewandte Chemie 119, no. 48 (December 10, 2007): 9371–74. http://dx.doi.org/10.1002/ange.200704122.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Youngsaye, Willmen, Jason T Lowe, Frauke Pohlki, Paul Ralifo, and James S Panek. "Total Synthesis and Stereochemical Reassignment of (+)-Neopeltolide." Angewandte Chemie International Edition 46, no. 48 (December 10, 2007): 9211–14. http://dx.doi.org/10.1002/anie.200704122.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Paterson, Ian, and Natalie A. Miller. "Total synthesis of the marine macrolide (+)-neopeltolide." Chemical Communications, no. 39 (2008): 4708. http://dx.doi.org/10.1039/b812914b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Meissner, Andreas, Nobuhiro Tanaka, Hiroyoshi Takamura, and Isao Kadota. "Stereocontrolled synthesis of the macrolactone core of neopeltolide." Tetrahedron Letters 60, no. 5 (January 2019): 432–34. http://dx.doi.org/10.1016/j.tetlet.2018.12.066.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Cui, Yubo, Raghavan Balachandran, Billy W. Day, and Paul E. Floreancig. "Synthesis and Biological Evaluation of Neopeltolide and Analogs." Journal of Organic Chemistry 77, no. 5 (February 22, 2012): 2225–35. http://dx.doi.org/10.1021/jo2023685.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Fuwa, Haruhiko, Asami Saito, and Makoto Sasaki. "ChemInform Abstract: A Concise Total Synthesis of (+)-Neopeltolide." ChemInform 41, no. 33 (July 24, 2010): no. http://dx.doi.org/10.1002/chin.201033211.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Woo, Sang Kook, Min Sang Kwon, and Eun Lee. "Total Synthesis of (+)-Neopeltolide by a Prins Macrocyclization." Angewandte Chemie 120, no. 17 (April 14, 2008): 3286–88. http://dx.doi.org/10.1002/ange.200800386.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Woo, Sang Kook, Min Sang Kwon, and Eun Lee. "Total Synthesis of (+)-Neopeltolide by a Prins Macrocyclization." Angewandte Chemie International Edition 47, no. 17 (April 14, 2008): 3242–44. http://dx.doi.org/10.1002/anie.200800386.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Raghavan, Sadagopan, and Pradip Kumar Samanta. "Stereoselective Synthesis of the Macrolactone Core of (+)-Neopeltolide." Organic Letters 14, no. 9 (April 19, 2012): 2346–49. http://dx.doi.org/10.1021/ol3007698.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Fuwa, Haruhiko, Kenkichi Noto, Masato Kawakami, and Makoto Sasaki. "Synthesis and Biological Evaluation of Aspergillide A/Neopeltolide Chimeras." Chemistry Letters 42, no. 9 (September 5, 2013): 1020–22. http://dx.doi.org/10.1246/cl.130322.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Vintonyak, Viktor V, Brigitte Kunze, Florenz Sasse, and Martin E Maier. "Total Synthesis and Biological Activity of Neopeltolide and Analogues." Chemistry - A European Journal 14, no. 35 (December 8, 2008): 11132–40. http://dx.doi.org/10.1002/chem.200801398.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Ghosh, Arun K., Khriesto A. Shurrush, and Zachary L. Dawson. "ChemInform Abstract: Enantioselective Total Synthesis of Macrolide (+)-Neopeltolide (I)." ChemInform 45, no. 13 (March 14, 2014): no. http://dx.doi.org/10.1002/chin.201413237.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Custar, Daniel W., Thomas P. Zabawa, and Karl A. Scheidt. "Total Synthesis and Structural Revision of the Marine Macrolide Neopeltolide." Journal of the American Chemical Society 130, no. 3 (January 2008): 804–5. http://dx.doi.org/10.1021/ja710080q.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Tu, Wangyang, and Paul E Floreancig. "Oxidative Carbocation Formation in Macrocycles: Synthesis of the Neopeltolide Macrocycle." Angewandte Chemie International Edition 48, no. 25 (June 8, 2009): 4567–71. http://dx.doi.org/10.1002/anie.200901489.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Fuwa, Haruhiko, Asami Saito, Shinya Naito, Keiichi Konoki, Mari Yotsu-Yamashita, and Makoto Sasaki. "Total Synthesis and Biological Evaluation of (+)-Neopeltolide and Its Analogues." Chemistry - A European Journal 15, no. 46 (November 23, 2009): 12807–18. http://dx.doi.org/10.1002/chem.200901675.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Tu, Wangyang, and Paul E Floreancig. "Oxidative Carbocation Formation in Macrocycles: Synthesis of the Neopeltolide Macrocycle." Angewandte Chemie 121, no. 25 (June 8, 2009): 4637–41. http://dx.doi.org/10.1002/ange.200901489.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Sharma, Gangavaram V. M., Sheri Venkat Reddy, and Kallaganti V. S. Ramakrishna. "Synthesis of the macrolactone core of (+)-neopeltolide by transannular cyclization." Organic & Biomolecular Chemistry 10, no. 18 (2012): 3689. http://dx.doi.org/10.1039/c2ob25151e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Wright, Amy E., Julianne Cook Botelho, Esther Guzmán, Dedra Harmody, Patricia Linley, Peter J. McCarthy, Tara P. Pitts, Shirley A. Pomponi, and John K. Reed. "Neopeltolide, a Macrolide from a Lithistid Sponge of the Family Neopeltidae⊥." Journal of Natural Products 70, no. 3 (March 2007): 412–16. http://dx.doi.org/10.1021/np060597h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Kartika, Rendy, Thomas R. Gruffi, and Richard E. Taylor. "Concise Enantioselective Total Synthesis of Neopeltolide Macrolactone Highlighted by Ether Transfer." Organic Letters 10, no. 21 (November 6, 2008): 5047–50. http://dx.doi.org/10.1021/ol802254z.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Ulanovskaya, Olesya A., Jelena Janjic, Masato Suzuki, Simran S. Sabharwal, Paul T. Schumacker, Stephen J. Kron, and Sergey A. Kozmin. "Synthesis enables identification of the cellular target of leucascandrolide A and neopeltolide." Nature Chemical Biology 4, no. 7 (May 30, 2008): 418–24. http://dx.doi.org/10.1038/nchembio.94.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Custar, Daniel W., Thomas P. Zabawa, John Hines, Craig M. Crews, and Karl A. Scheidt. "Total Synthesis and Structure−Activity Investigation of the Marine Natural Product Neopeltolide." Journal of the American Chemical Society 131, no. 34 (September 2, 2009): 12406–14. http://dx.doi.org/10.1021/ja904604x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Martinez-Solorio, Dionicio, and Michael P. Jennings. "Formal Synthesis of (−)-Neopeltolide Featuring a Highly Stereoselective Oxocarbenium Formation/Reduction Sequence." Journal of Organic Chemistry 75, no. 12 (June 18, 2010): 4095–104. http://dx.doi.org/10.1021/jo100443h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Hari, Taylor P. A., Burkardt I. Wilke, James A. Davey, and Christopher N. Boddy. "Diastereoseletive Transannular Oxa-Conjugate Addition Generates the 2,6-cis-Disubstituted Tetrahydropyran of Neopeltolide." Journal of Organic Chemistry 81, no. 2 (December 29, 2015): 415–23. http://dx.doi.org/10.1021/acs.joc.5b02014.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Bai, Yu, and Mingji Dai. "Strategies and Methods for the Synthesis of Anticancer Natural Product Neopeltolide and its Analogs." Current Organic Chemistry 19, no. 10 (May 27, 2015): 871–85. http://dx.doi.org/10.2174/1385272819666150119225149.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Yadav, Jhillu Singh, Gunda Gopala Krishana, and Satya Narayana Kumar. "A concise stereoselective formal total synthesis of the cytotoxic macrolide (+)-Neopeltolide via Prins cyclization." Tetrahedron 66, no. 2 (January 2010): 480–87. http://dx.doi.org/10.1016/j.tet.2009.11.054.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Florence, Gordon J., and Romain F. Cadou. "Studies towards the synthesis of neopeltolide: synthesis of a ring-closing metathesis macrocyclization precursor." Tetrahedron Letters 51, no. 44 (November 2010): 5761–63. http://dx.doi.org/10.1016/j.tetlet.2010.08.118.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Davyt, Danilo, and Gloria Serra. "ChemInform Abstract: Synthesis and Biological Activity of Promising Azole Marine Products. Largazole and Neopeltolide." ChemInform 44, no. 31 (July 11, 2013): no. http://dx.doi.org/10.1002/chin.201331255.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Fuwa, Haruhiko, Takuma Noguchi, Masato Kawakami, and Makoto Sasaki. "Synthesis and biological evaluation of (+)-neopeltolide analogues: Importance of the oxazole-containing side chain." Bioorganic & Medicinal Chemistry Letters 24, no. 11 (June 2014): 2415–19. http://dx.doi.org/10.1016/j.bmcl.2014.04.031.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Xiong, Mao-Qian, Tao Chen, Yu-Xia Wang, Xiao-Lei Zhu, and Guang-Fu Yang. "Design and synthesis of potent inhibitors of bc1 complex based on natural product neopeltolide." Bioorganic & Medicinal Chemistry Letters 30, no. 16 (August 2020): 127324. http://dx.doi.org/10.1016/j.bmcl.2020.127324.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Zhu, Xiao-Lei, Rui Zhang, Qiong-You Wu, Yong-Jun Song, Yu-Xia Wang, Jing-Fang Yang, and Guang-Fu Yang. "Natural Product Neopeltolide as a Cytochrome bc1 Complex Inhibitor: Mechanism of Action and Structural Modification." Journal of Agricultural and Food Chemistry 67, no. 10 (February 22, 2019): 2774–81. http://dx.doi.org/10.1021/acs.jafc.8b06195.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Hartmann, Eduard, and Martin Oestreich. "Asymmetric Conjugate Silyl Transfer in Iterative Catalytic Sequences: Synthesis of the C7-C16 Fragment of (+)-Neopeltolide." Angewandte Chemie International Edition 49, no. 35 (July 20, 2010): 6195–98. http://dx.doi.org/10.1002/anie.201002916.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Fuwa, Haruhiko, and Mizuho Sato. "A Synthetic Analogue of Neopeltolide, 8,9-Dehydroneopeltolide, Is a Potent Anti-Austerity Agent against Starved Tumor Cells." Marine Drugs 15, no. 10 (October 20, 2017): 320. http://dx.doi.org/10.3390/md15100320.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Yu, Miao, Richard R. Schrock, and Amir H. Hoveyda. "Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multistep Synthesis Design: A Concise Route to (+)-Neopeltolide." Angewandte Chemie 127, no. 1 (November 6, 2014): 217–22. http://dx.doi.org/10.1002/ange.201409120.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Yu, Miao, Richard R. Schrock, and Amir H. Hoveyda. "Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multistep Synthesis Design: A Concise Route to (+)-Neopeltolide." Angewandte Chemie International Edition 54, no. 1 (November 6, 2014): 215–20. http://dx.doi.org/10.1002/anie.201409120.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Fuwa, Haruhiko. "Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural Product." Marine Drugs 14, no. 4 (March 25, 2016): 65. http://dx.doi.org/10.3390/md14040065.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!