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Journal articles on the topic 'Vinigrol'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Maimone, Thomas J., Jun Shi, Shinji Ashida, and Phil S. Baran. "Total Synthesis of Vinigrol." Journal of the American Chemical Society 131, no. 47 (December 2, 2009): 17066–67. http://dx.doi.org/10.1021/ja908194b.

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2

Yang, Qingliang, Jon T. Njardarson, Cristian Draghici, and Fang Li. "Total Synthesis of Vinigrol." Angewandte Chemie International Edition 52, no. 33 (July 1, 2013): 8648–51. http://dx.doi.org/10.1002/anie.201304624.

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3

Yang, Qingliang, Jon T. Njardarson, Cristian Draghici, and Fang Li. "Total Synthesis of Vinigrol." Angewandte Chemie 125, no. 33 (July 1, 2013): 8810–13. http://dx.doi.org/10.1002/ange.201304624.

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4

Wang, Xian-Lei, Yun-Yu Lu, Jie Wang, Xuan Wang, He-Quan Yao, Guo-Qiang Lin, and Bing-Feng Sun. "A novel synthetic approach to the bicyclo[5.3.1]undecan-11-one framework of vinigrol." Org. Biomol. Chem. 12, no. 22 (2014): 3562–66. http://dx.doi.org/10.1039/c4ob00046c.

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Abstract:

A unique approach to the [5.3.1] bicyclic core of vinigrol is described featuring highly stereoselective C–C bond forming reactions through exploring the inherent conformational bias of the cyclooctane-ring system.

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5

Min, Long, Xiaohong Lin, and Chuang-Chuang Li. "Asymmetric Total Synthesis of (−)-Vinigrol." Journal of the American Chemical Society 141, no. 40 (September 23, 2019): 15773–78. http://dx.doi.org/10.1021/jacs.9b08983.

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6

Maimone, Thomas J, Ana-Florina Voica, and Phil S Baran. "Ein einfacher Zugang zu Vinigrol." Angewandte Chemie 120, no. 16 (April 7, 2008): 3097–99. http://dx.doi.org/10.1002/ange.200800167.

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7

Poulin, Jason, Christiane M. Grisé-Bard, and Louis Barriault. "A Formal Synthesis of Vinigrol." Angewandte Chemie 124, no. 9 (January 19, 2012): 2153–56. http://dx.doi.org/10.1002/ange.201108779.

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8

Huters, Alexander D, and Neil K Garg. "Synthetic Studies Inspired by Vinigrol." Chemistry - A European Journal 16, no. 29 (July 2, 2010): 8586–95. http://dx.doi.org/10.1002/chem.201000916.

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9

Maimone, Thomas J, Ana-Florina Voica, and Phil S Baran. "A Concise Approach to Vinigrol." Angewandte Chemie International Edition 47, no. 16 (April 7, 2008): 3054–56. http://dx.doi.org/10.1002/anie.200800167.

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10

Poulin, Jason, Christiane M. Grisé-Bard, and Louis Barriault. "A Formal Synthesis of Vinigrol." Angewandte Chemie International Edition 51, no. 9 (January 19, 2012): 2111–14. http://dx.doi.org/10.1002/anie.201108779.

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11

Yu, Xuerong, Lianghong Xiao, Zechun Wang, and Tuoping Luo. "Scalable Total Synthesis of (−)-Vinigrol." Journal of the American Chemical Society 141, no. 8 (February 15, 2019): 3440–43. http://dx.doi.org/10.1021/jacs.9b00621.

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12

Lu, Jin-Yong, and Dennis G Hall. "Totalsynthese von Vinigrol: Komplexität durch Fragmentierung." Angewandte Chemie 122, no. 13 (February 24, 2010): 2336–38. http://dx.doi.org/10.1002/ange.200906826.

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13

Betkekar, Vipul V., and Krishna P. Kaliappan. "Strategic innovations for the synthesis of vinigrol." Tetrahedron Letters 59, no. 26 (June 2018): 2485–501. http://dx.doi.org/10.1016/j.tetlet.2018.05.049.

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14

Morton, Jason G. M., Laura D. Kwon, John D. Freeman, and Jon T. Njardarson. "An Adler–Becker oxidation approach to vinigrol." Tetrahedron Letters 50, no. 15 (April 2009): 1684–86. http://dx.doi.org/10.1016/j.tetlet.2009.01.134.

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15

Huters, Alexander D., and Neil K. Garg. "ChemInform Abstract: Synthetic Studies Inspired by Vinigrol." ChemInform 41, no. 48 (November 4, 2010): no. http://dx.doi.org/10.1002/chin.201048237.

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16

Gentric, Lionel, Issam Hanna, and Louis Ricard. "Synthesis of the Complete Carbocyclic Skeleton of Vinigrol." Organic Letters 5, no. 7 (April 2003): 1139–42. http://dx.doi.org/10.1021/ol034217k.

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17

Tessier, Guillaume, and Louis Barriault. "THE CONQUEST OF VINIGROL. CREATIVITY, FRUSTRATIONS, AND HOPE." Organic Preparations and Procedures International 39, no. 4 (August 2007): 311–53. http://dx.doi.org/10.1080/00304940709458591.

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18

Min, Long, and Chuang-Chuang Li. "Recent advances in the total synthesis of vinigrol." Chinese Science Bulletin 66, no. 25 (May 13, 2021): 3230–40. http://dx.doi.org/10.1360/tb-2021-0188.

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19

Draghici, Cristian, and Jon T. Njardarson. "Synthetic approaches and total syntheses of vinigrol, a unique diterpenoid." Tetrahedron 71, no. 23 (June 2015): 3775–93. http://dx.doi.org/10.1016/j.tet.2015.04.073.

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20

Lu, Jin-Yong, and Dennis G Hall. "Fragmentation Enables Complexity in the First Total Synthesis of Vinigrol." Angewandte Chemie International Edition 49, no. 13 (February 24, 2010): 2286–88. http://dx.doi.org/10.1002/anie.200906826.

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21

Devaux, Jean Francois, Issam Hanna, Jean Yves Lallemand, and Thierry Prange. "A short synthesis of the tricyclic ring system of vinigrol." Journal of Organic Chemistry 58, no. 9 (April 1993): 2349–50. http://dx.doi.org/10.1021/jo00061a002.

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22

Yang, Qingliang, Cristian Draghici, Jon T. Njardarson, Fang Li, Brandon R. Smith, and Pradipta Das. "Evolution of an oxidative dearomatization enabled total synthesis of vinigrol." Org. Biomol. Chem. 12, no. 2 (2014): 330–44. http://dx.doi.org/10.1039/c3ob42191k.

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23

Betkekar, Vipul V., Ashik A. Sayyad, and Krishna P. Kaliappan. "A Domino Enyne/IMDA Approach to the Core Structure of (−) Vinigrol." Organic Letters 16, no. 21 (October 13, 2014): 5540–43. http://dx.doi.org/10.1021/ol502497n.

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24

Lu, Jin-Yong, and Dennis G. Hall. "ChemInform Abstract: Fragmentation Enables Complexity in the First Total Synthesis of Vinigrol." ChemInform 41, no. 26 (June 8, 2010): no. http://dx.doi.org/10.1002/chin.201026258.

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25

Gentric, Lionel, Xavier Le Goff, Louis Ricard, and Issam Hanna. "Toward the Total Synthesis of Vinigrol: Synthesis of epi-C-8-Dihydrovinigrol." Journal of Organic Chemistry 74, no. 24 (December 18, 2009): 9337–44. http://dx.doi.org/10.1021/jo901971f.

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26

Morency, Louis, and Louis Barriault. "Studies toward the Total Synthesis of Vinigrol. Synthesis of the Octalin Ring." Journal of Organic Chemistry 70, no. 22 (October 2005): 8841–53. http://dx.doi.org/10.1021/jo051318i.

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27

Souweha, Michael Santos, Gary D. Enright, and Alex G. Fallis. "Vinigrol: A Compact, Diene-Transmissive Diels−Alder Strategy to the Tricyclic Core." Organic Letters 9, no. 25 (December 2007): 5163–66. http://dx.doi.org/10.1021/ol702202b.

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28

Draghici, Cristian, and Jon T. Njardarson. "ChemInform Abstract: Synthetic Approaches and Total Syntheses of Vinigrol, a Unique Diterpenoid." ChemInform 46, no. 29 (July 2015): no. http://dx.doi.org/10.1002/chin.201529278.

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29

Grisé,, Christiane M., Guillaume Tessier, and Louis Barriault. "Synthesis of the Tricyclic Core of Vinigrol via an Intramolecular Diels−Alder Reaction." Organic Letters 9, no. 8 (April 2007): 1545–48. http://dx.doi.org/10.1021/ol0702977.

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30

Devaux, Jean-François, Issam Hanna, and Jean-Yves Lallemand. "Studies toward the Synthesis of Vinigrol. First Construction of the Tricyclic Ring System." Journal of Organic Chemistry 62, no. 15 (July 1997): 5062–68. http://dx.doi.org/10.1021/jo970343o.

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31

Yang, Qingliang, Cristian Draghici, Jon T. Njardarson, Fang Li, Brandon R. Smith, and Pradipta Das. "ChemInform Abstract: Evolution of an Oxidative Dearomatization Enabled Total Synthesis of Vinigrol (I)." ChemInform 45, no. 25 (June 5, 2014): no. http://dx.doi.org/10.1002/chin.201425205.

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32

Kito, M., T. Sakai, H. Shirahama, M. Miyashita, and F. Matsuda. "Construction of 8-Membered Ring Skeleton of Vinigrol via SmI2-Promoted Barbier Coupling." Synlett 1997, no. 2 (February 1997): 219–20. http://dx.doi.org/10.1055/s-1997-748.

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33

Uchida, Itsuo, Takeshi Ando, Naoki Fukami, Keizo Yoshida, Masashi Hashimoto, Toshiji Tada, Shigetaka Koda, and Yukiyoshi Morimoto. "The structure of vinigrol, a novel diterpenoid with antihypertensive and platelet aggregation-inhibitory activities." Journal of Organic Chemistry 52, no. 23 (November 1987): 5292–93. http://dx.doi.org/10.1021/jo00232a048.

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34

Matsuda, Fuyuhiko, Makoto Kito, Toshinari Sakai, Naoko Okada, Masaaki Miyashita, and Haruhisa Shirahama. "Efficient construction of 8-membered ring framework of vinigrol through SmI2-induced coupling cyclization." Tetrahedron 55, no. 50 (December 1999): 14369–80. http://dx.doi.org/10.1016/s0040-4020(99)00885-6.

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35

Njardarson, Jon, Jason Morton, Laura Kwon, and John Freeman. "Thieme Chemistry Journal Awardees - Where are They Now? Efforts towards the Total Synthesis of Vinigrol." Synlett 2009, no. 01 (December 12, 2008): 23–27. http://dx.doi.org/10.1055/s-0028-1087378.

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36

Morency, Louis, and Louis Barriault. "Stereoselective synthesis of the cis-decalin subunit of vinigrol via three pericyclic reactions in cascade." Tetrahedron Letters 45, no. 32 (August 2004): 6105–7. http://dx.doi.org/10.1016/j.tetlet.2004.06.071.

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37

DEVAUX, J. F., I. HANNA, and J. Y. LALLEMAND. "ChemInform Abstract: Studies Toward the Synthesis of Vinigrol. First Construction of the Tricyclic Ring System." ChemInform 28, no. 52 (August 2, 2010): no. http://dx.doi.org/10.1002/chin.199752198.

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38

KITO, M., T. SAKAI, H. SHIRAHAMA, M. MIYASHITA, and F. MATSUDA. "ChemInform Abstract: Construction of 8-Membered Ring Skeleton of Vinigrol via SmI2-Promoted Barbier Coupling." ChemInform 28, no. 27 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199727194.

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39

Lu, Yan-Bin, Day-Shin Hsu, and Chun-Chen Liao. "Rapid construction of polycyclic ring systems from aromatics: stereoselective synthesis of the carbon framework of vinigrol." Tetrahedron Letters 55, no. 38 (September 2014): 5315–18. http://dx.doi.org/10.1016/j.tetlet.2014.07.064.

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40

DEVAUX, J. F., I. HANNA, J. Y. LALLEMAND, and T. PRANGE. "ChemInform Abstract: An Unexpected Acid-Catalyzed Rearrangement of the Tricyclic System of Vinigrol to the Fusoxysporone Skeleton." ChemInform 27, no. 28 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199628229.

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41

Kito, M., T. Sakai, N. Haruta, H. Shirahama, and F. Matsuda. "Stereoselective Cyclization of cis-Decalin Skeleton of Vinigrol via Ketyl-Olefin Coupling Promoted by Samarium(II) Iodide." Synlett 1996, no. 11 (December 31, 2000): 1057–60. http://dx.doi.org/10.1055/s-1996-5697.

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42

Paquette, Leo A., and Ivan Efremov. "Exploratory Studies Aimed at a Synthesis of Vinigrol. 3. Evaluation of a Lactone Bridge as a Conformational Lock." Journal of Organic Chemistry 70, no. 2 (January 2005): 510–13. http://dx.doi.org/10.1021/jo0484575.

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43

Wang, Xian-Lei, Yun-Yu Lu, Jie Wang, Xuan Wang, He-Quan Yao, Guo-Qiang Lin, and Bing-Feng Sun. "ChemInform Abstract: A Novel Synthetic Approach to the Bicyclo[5.3.1]undecan-11-one Framework (I) of Vinigrol (II)." ChemInform 45, no. 44 (October 16, 2014): no. http://dx.doi.org/10.1002/chin.201444210.

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44

ANDO, TAKESHI, KEIZO YOSHIDA, and MASAKUNI OKUHARA. "Vinigrol, a novel antihypertensive and platelet aggregation inhibitory agent produced by a fungus, Virgaria nigra. II. Pharmacological characteristics." Journal of Antibiotics 41, no. 1 (1988): 31–35. http://dx.doi.org/10.7164/antibiotics.41.31.

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45

Mehta, Goverdhan, and K. Subba Reddy. "A Facile Oxy-Cope Rearrangement Route to Functionalized Bicyclo[5.3.1]undecane Ring System Present in Taxol and Vinigrol Diterpenoids." Synlett 1996, no. 07 (July 1996): 625–27. http://dx.doi.org/10.1055/s-1996-5557.

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46

Ma, Jialin, and Mengtao Sun. "Photo-physical properties of vinigrol revealed by two-photon absorption, electronic circular dichroism, Raman spectroscopy and Raman optical activity." Chemical Physics Letters 755 (September 2020): 137798. http://dx.doi.org/10.1016/j.cplett.2020.137798.

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47

KITO, M., T. SAKAI, N. HARUTA, H. SHIRAHAMA, and F. MATSUDA. "ChemInform Abstract: Stereoselective Cyclization of the cis-Decalin Skeleton of Vinigrol via Ketyl-Olefin Coupling Promoted by Samarium(II) Iodide." ChemInform 28, no. 15 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199715189.

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48

MEHTA, G., and K. S. REDDY. "ChemInform Abstract: A Facile Oxy-Cope Rearrangement Route to Functionalized Bicyclo(5.3.1) undecane Ring System Present in Taxol and Vinigrol Diterpenoids." ChemInform 27, no. 49 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199649209.

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49

Paquette, Leo A., Ivan Efremov, and Zuosheng Liu. "Exploratory Studies Aimed at a Synthesis of Vinigrol. 2. Attempts to Exploit Ring-Closing Metathesis for Construction of the Central Cyclooctane Belt." Journal of Organic Chemistry 70, no. 2 (January 2005): 505–9. http://dx.doi.org/10.1021/jo048458x.

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50

ANDO, TAKESHI, YASUHISA TSURUMI, NOBUTAKA OHATA, ITSUO UCHIDA, KEIZO YOSHIDA, and MASAKUNI OKUHARA. "Vinigrol, a novel antihypertensive and platelet aggregation inhibitory agent produced by a fungus, Virgaria nigra. I. Taxonomy, fermentation, isolation, physico-chemical and biological properties." Journal of Antibiotics 41, no. 1 (1988): 25–30. http://dx.doi.org/10.7164/antibiotics.41.25.

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