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Journal articles on the topic 'Total synthesis of GA18'

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Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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1

Jain, Rakesh K., Rakesh Vig, Rajit Rampal, E. V. Chandrasekaran, and Khushi L. Matta. "Total Synthesis of 3'-O-Sialyl, 6'-O-Sulfo Lewisx, NeuAc.alpha.2.fwdarw.3(6-O-SO3Na)Ga1.beta.1.fwdarw.4(Fuc.alpha.1.fwdarw.3)GlcNAc.beta.-OMe: A Major Capping Group of GLYCAM-I." Journal of the American Chemical Society 116, no. 26 (December 1994): 12123–24. http://dx.doi.org/10.1021/ja00105a091.

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2

Zeelen, F. J. "Steroid total synthesis." Natural Product Reports 11, no. 6 (1994): 607. http://dx.doi.org/10.1039/np9941100607.

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3

WILSON, ELIZABETH. "TOTAL SYNTHESIS SURPRISE." Chemical & Engineering News 79, no. 51 (December 17, 2001): 11. http://dx.doi.org/10.1021/cen-v079n051.p011.

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4

Groen, M. B., and F. J. Zeelen. "Steroid total synthesis." Recueil des Travaux Chimiques des Pays-Bas 105, no. 11 (1986): 465–87. http://dx.doi.org/10.1002/recl.19861051102.

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5

Mori, Tomonori, Shuhei Higashibayashi, Taiji Goto, Mitsunori Kohno, Yukiko Satouchi, Kazuyuki Shinko, Kengo Suzuki, et al. "Total Synthesis of Siomycin A: Completion of the Total Synthesis." Chemistry – An Asian Journal 3, no. 6 (June 2, 2008): 1013–25. http://dx.doi.org/10.1002/asia.200800033.

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6

Wang, Bo, T. Matthew Hansen, Lynn Weyer, Dimao Wu, Ting Wang, Mathias Christmann, Yingtao Lu, et al. "Total Synthesis of Phorboxazole A viade NovoOxazole Formation: Convergent Total Synthesis." Journal of the American Chemical Society 133, no. 5 (February 9, 2011): 1506–16. http://dx.doi.org/10.1021/ja1089099.

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7

Nakata, Tadashi, Shigeto Nagao, and Takeshi Oishi. "Total synthesis of (+)-pederin. 2. Stereocontrolled synthesis of (+)-benzoylselenopederic acid and total synthesis of (+)-pederin." Tetrahedron Letters 26, no. 52 (January 1985): 6465–68. http://dx.doi.org/10.1016/s0040-4039(00)99028-2.

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8

Thomas, Eric J., and John W. F. Whitehead. "Cytochalasan synthesis: total synthesis of cytochalasin H." Journal of the Chemical Society, Perkin Transactions 1, no. 3 (1989): 507. http://dx.doi.org/10.1039/p19890000507.

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9

Dyke, Hazel, Patrick G. Steel, and Eric J. Thomas. "Cytochalasan synthesis: total synthesis of cytochalasin G." Journal of the Chemical Society, Perkin Transactions 1, no. 3 (1989): 525. http://dx.doi.org/10.1039/p19890000525.

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10

Thomas, Eric J., and John W. F. Whitehead. "Cytochalasan synthesis: total synthesis of cytochalasin H." Journal of the Chemical Society, Chemical Communications, no. 9 (1986): 727. http://dx.doi.org/10.1039/c39860000727.

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11

Dyke, Hazel, Robert Sauter, Patrick Steel, and Eric J. Thomas. "Cytochalasan synthesis: total synthesis of cytochalasin G." Journal of the Chemical Society, Chemical Communications, no. 18 (1986): 1447. http://dx.doi.org/10.1039/c39860001447.

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12

Merifield, Eric, and Eric J. Thomas. "Cytochalasan synthesis: total synthesis of cytochalasin D." Journal of the Chemical Society, Chemical Communications, no. 6 (1990): 464. http://dx.doi.org/10.1039/c39900000464.

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13

Warmuth, Lucas, Aaron Weiß, Marco Reinhardt, Anna Meschkov, Ute Schepers, and Joachim Podlech. "Total synthesis of decarboxyaltenusin." Beilstein Journal of Organic Chemistry 17 (January 22, 2021): 224–28. http://dx.doi.org/10.3762/bjoc.17.22.

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The total synthesis of decarboxyaltenusin (5’-methoxy-6-methyl-[1,1’-biphenyl]-3,3’,4-triol), a toxin produced by various mold fungi, has been achieved in seven steps in a yield of 31% starting from 4-methylcatechol and 1-bromo-3,5-dimethoxybenzene, where the longest linear sequence consists of five steps. The key reaction was a palladium-catalyzed Suzuki coupling of an aromatic boronate with a brominated resorcin derivative.

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14

Nagasawa, Kazuo. "Total Synthesis of Saxitoxins." Journal of Synthetic Organic Chemistry, Japan 79, no. 1 (January 1, 2021): 43–53. http://dx.doi.org/10.5059/yukigoseikyokaishi.79.43.

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15

Ndoile, Monica M., and Fanie R. van Heerden. "Total synthesis of ochnaflavone." Beilstein Journal of Organic Chemistry 9 (July 8, 2013): 1346–51. http://dx.doi.org/10.3762/bjoc.9.152.

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The first total syntheses of ochnaflavone, an asymmetric biflavone consisting of apigenin and luteolin moieties, and the permethyl ether of 2,3,2'',3''-tetrahydroochnaflavone have been achieved. The key steps in the synthesis of ochnaflavone were the formation of a diaryl ether and ring cyclization of an ether-linked dimeric chalcone to assemble the two flavone nuclei. Optimal experimental conditions for the oxidative cyclization to form ochnaflavone were established.

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16

Hess, Stephan N., Xiaobin Mo, Conny Wirtz, and Alois Fürstner. "Total Synthesis of Limaol." Journal of the American Chemical Society 143, no. 6 (February 3, 2021): 2464–69. http://dx.doi.org/10.1021/jacs.0c12948.

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17

Singh, Vipin Kumar, and Tushar Kanti Chakraborty. "Total Synthesis of Panaginsene." Chemistry – An Asian Journal 16, no. 7 (March 8, 2021): 753–56. http://dx.doi.org/10.1002/asia.202100144.

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18

Namba, Kosuke, Kohei Takeuchi, Yukari Kaihara, and Keiji Tanino. "Total Synthesis of Palau’amine." Journal of Synthetic Organic Chemistry, Japan 75, no. 11 (2017): 1094–101. http://dx.doi.org/10.5059/yukigoseikyokaishi.75.1094.

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19

Nagasawa, Kazuo. "Total Synthesis of Saxitoxins." Journal of Synthetic Organic Chemistry, Japan 79, no. 1 (January 1, 2021): 43–53. http://dx.doi.org/10.5059/yukigoseikyokaishi.79.43.

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20

Wang, Feng‐Yuan, and Lei Jiao. "Total Synthesis of (−)‐Arborisidine." Angewandte Chemie 133, no. 23 (April 28, 2021): 12842–46. http://dx.doi.org/10.1002/ange.202101161.

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21

Wang, Feng‐Yuan, and Lei Jiao. "Total Synthesis of (−)‐Arborisidine." Angewandte Chemie International Edition 60, no. 23 (April 28, 2021): 12732–36. http://dx.doi.org/10.1002/anie.202101161.

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22

Nakagawa, Masako, Manabu Ito, Yuko Hasegawa, Satoko Akashi, Mikio Taniguchi, and Tohru Hino. "Total Synthesis of Triptoquivalines." HETEROCYCLES 23, no. 1 (1985): 224. http://dx.doi.org/10.3987/r-1985-01-0224.

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23

Suzuki, Toshio, Etsuko Sato, Katsuo Unno, and Tetsuji Kametani. "Total Synthesis of (-)-Antirhine." HETEROCYCLES 23, no. 4 (1985): 839. http://dx.doi.org/10.3987/r-1985-04-0839.

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24

J. de Souza, Noel, Bipin D. Alreja, Samba L. Kattige, and Bansi Lal. "Total Synthesis of Caerulomycin." HETEROCYCLES 24, no. 6 (1986): 1637. http://dx.doi.org/10.3987/r-1986-06-1637.

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25

Mori, Miwako. "Total Synthesis of Strychnine." HETEROCYCLES 81, no. 2 (2010): 259. http://dx.doi.org/10.3987/rev-09-661.

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26

Mori, Yuji. "Total Synthesis of Gambierol." HETEROCYCLES 81, no. 10 (2010): 2203. http://dx.doi.org/10.3987/rev-10-676.

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27

Nagasawa, Kazuo, Minami Odagi, Kota Furukori, and Yoshiharu Yamamoto. "Total Synthesis of (+)-Linoxepin." HETEROCYCLES 95, no. 1 (2017): 116. http://dx.doi.org/10.3987/rev-16-sr(s)3.

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28

Ishikura, Minoru, Katsuaki Imaizumi, and Nobuya Katagiri. "Total Synthesis of Yuehchukene." HETEROCYCLES 53, no. 3 (2000): 553. http://dx.doi.org/10.3987/com-99-8822.

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29

MATSUDA, Fuyuhiko, and Shiro TERASHIMA. "Total synthesis of sesbanimides." Journal of Synthetic Organic Chemistry, Japan 45, no. 10 (1987): 983–91. http://dx.doi.org/10.5059/yukigoseikyokaishi.45.983.

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30

KAWAMURA, Kuniaki, R. J. DeVita, and A. S. Kende. "Total Synthesis of Neooxazolomycin." Journal of Synthetic Organic Chemistry, Japan 50, no. 1 (1992): 61–70. http://dx.doi.org/10.5059/yukigoseikyokaishi.50.61.

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31

KATOH, Tadashi, and Shiro TERASHIMA. "Total Synthesis of Quinocarcin." Journal of Synthetic Organic Chemistry, Japan 52, no. 7 (1994): 556–71. http://dx.doi.org/10.5059/yukigoseikyokaishi.52.556.

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32

Fukuyama, Tohru, and Yutaka Kanda. "Total Synthesis of (+)-Leinamycin." Journal of Synthetic Organic Chemistry, Japan 52, no. 11 (1994): 888–99. http://dx.doi.org/10.5059/yukigoseikyokaishi.52.888.

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33

OIKAWA, Masato, Tohru UENO, Hideaki OIKAWA, and Akitami ICHIHARA. "Total Synthesis of Tautomycin." Journal of Synthetic Organic Chemistry, Japan 53, no. 12 (1995): 1123–32. http://dx.doi.org/10.5059/yukigoseikyokaishi.53.1123.

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34

Takayanagi, Masaru. "Total Synthesis of Vancomycin." Journal of Synthetic Organic Chemistry, Japan 60, no. 3 (2002): 240–49. http://dx.doi.org/10.5059/yukigoseikyokaishi.60.240.

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35

Kobayashi, Yuichi. "Total Synthesis of Macrosphelides." Journal of Synthetic Organic Chemistry, Japan 63, no. 3 (2005): 190–99. http://dx.doi.org/10.5059/yukigoseikyokaishi.63.190.

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36

Shishido, Kozo, Takeshi Takata, Koji Umimoto, and Masayuki Shibuya. "Total Synthesis of (+)-Menthofuran." HETEROCYCLES 33, no. 1 (1992): 73. http://dx.doi.org/10.3987/com-91-s19.

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37

Kubo, Akinori, Shinsuke Nakahara, and Yoshihiro Tanaka. "Total Synthesis of Eilatin." HETEROCYCLES 36, no. 5 (1993): 1139. http://dx.doi.org/10.3987/com-92-6322.

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38

Murai, Akio, and Lian-xun Gao. "Total Synthesis of (-)-Dactylynes." HETEROCYCLES 42, no. 2 (1996): 745. http://dx.doi.org/10.3987/com-95-s84.

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39

Kubo, Akinori, Shinsuke Nakahara, and Yoshihiro Tanaka. "Total Synthesis of Amphimedine." HETEROCYCLES 43, no. 10 (1996): 2113. http://dx.doi.org/10.3987/com-96-7476.

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40

Yadav, J. S., R. Satheesh Babu, and G. Sabitha. "Total synthesis of (+) artemisinin." Arkivoc 2003, no. 3 (March 19, 2003): 125–39. http://dx.doi.org/10.3998/ark.5550190.0004.313.

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41

Nakamura, Tenma, Dinda B. Pitna, Kogaku Kimura, Yukiko Yoshimoto, Tomoya Uchiyama, Takaya Mori, Ryosuke Kondo, et al. "Total synthesis of cynaropicrin." Organic & Biomolecular Chemistry 19, no. 27 (2021): 6038–44. http://dx.doi.org/10.1039/d1ob00657f.

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The first total synthesis of the sesquiterpene lactone cynaropicrin, isolated from artichoke, was achieved starting from (S)-α-pinene. The synthesis involved a stereoselective Favorskii rearrangement and a diastereoselective Barbier reaction.

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42

Iiyama, Shota, Keisuke Fukaya, Yu Yamaguchi, Ami Watanabe, Hiroaki Yamamoto, Shota Mochizuki, Ryosuke Saio, et al. "Total Synthesis of Paclitaxel." Organic Letters 24, no. 1 (December 14, 2021): 202–6. http://dx.doi.org/10.1021/acs.orglett.1c03851.

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43

D’Angelo, Kyan A., Carly K. Schissel, Bradley L. Pentelute, and Mohammad Movassaghi. "Total synthesis of himastatin." Science 375, no. 6583 (February 25, 2022): 894–99. http://dx.doi.org/10.1126/science.abm6509.

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The natural product himastatin has an unusual homodimeric structure that presents a substantial synthetic challenge. We report the concise total synthesis of himastatin from readily accessible precursors, incorporating a final-stage dimerization strategy that was inspired by a detailed consideration of the compound’s biogenesis. Combining this approach with a modular synthesis enabled expedient access to more than a dozen designed derivatives of himastatin, including synthetic probes that provide insight into its antibiotic activity.

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44

Lee, Sanghyeon, Byung-Gyu Kim, Sujeong Geum, Jiheon Kim, and Hee-Yoon Lee. "Total Synthesis of (±)-Jujuyane." Organic Letters 23, no. 12 (June 3, 2021): 4651–56. http://dx.doi.org/10.1021/acs.orglett.1c01391.

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45

Zhang, Zhi, Yunfeng Li, Rentao Zhang, and Xiaoming Yu. "Total Synthesis of Geldanamycin." Journal of Organic Chemistry 86, no. 21 (October 16, 2021): 15063–75. http://dx.doi.org/10.1021/acs.joc.1c01582.

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46

Kumar Palli, Kishore, Palash Ghosh, Shiva Krishna Avula, B. Sridhara Shanmukha Rao, Amol D. Patil, Subhash Ghosh, Gangarajula Sudhakar, Chada Raji Reddy, Prathama S. Mainkar, and Srivari Chandrasekhar. "Total synthesis of remdesivir." Tetrahedron Letters 88 (January 2022): 153590. http://dx.doi.org/10.1016/j.tetlet.2021.153590.

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47

Zeng, Xianhuang, and Dale L. Boger. "Total Synthesis of (−)-Strempeliopine." Journal of the American Chemical Society 143, no. 31 (July 29, 2021): 12412–17. http://dx.doi.org/10.1021/jacs.1c06913.

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48

Park, Jinjae, and Cheol-Hong Cheon. "Total Synthesis of Rucaparib." Journal of Organic Chemistry 87, no. 7 (March 23, 2022): 4813–17. http://dx.doi.org/10.1021/acs.joc.2c00083.

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49

Wang, Xu-Kun, Yue-Mei Jia, Yi-Xian Li, and Chu-Yi Yu. "Total Synthesis of Pseudouridimycin." Organic Letters 24, no. 2 (January 10, 2022): 511–15. http://dx.doi.org/10.1021/acs.orglett.1c03914.

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50

NAGAMITSU, Tohru, Yoshihiro HARIGAYA, and Satoshi OMURA. "Total synthesis of borrelidin." Proceedings of the Japan Academy, Series B 81, no. 7 (2005): 244–56. http://dx.doi.org/10.2183/pjab.81.244.

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