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Relevant bibliographies by topics / Hamigeran

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Journal articles

Academic literature on the topic 'Hamigeran'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 September 2023

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Journal articles on the topic "Hamigeran"

1

Taber, Douglass F., and Weiwei Tian. "Synthesis of (−)-Hamigeran B." Journal of Organic Chemistry 73, no. 19 (2008): 7560–64. http://dx.doi.org/10.1021/jo8010683.

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2

Clive, Derrick L. J., and Jian Wang. "Synthesis of natural (−)-hamigeran B." Tetrahedron Letters 44, no. 42 (2003): 7731–33. http://dx.doi.org/10.1016/j.tetlet.2003.08.089.

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3

Clive, Derrick L. J., and Jian Wang. "Synthesis of (±)-Hamigeran B, (−)-Hamigeran B, and (±)-1-epi-Hamigeran B: Use of Bulky Silyl Groups to Protect a Benzylic Carbon−Oxygen Bond from Hydrogenolysis." Journal of Organic Chemistry 69, no. 8 (2004): 2773–84. http://dx.doi.org/10.1021/jo030347v.

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4

Jiang, Biao, Ming-ming Li, Ping Xing, and Zuo-gang Huang. "A Concise Formal Synthesis of (−)-Hamigeran B." Organic Letters 15, no. 4 (2013): 871–73. http://dx.doi.org/10.1021/ol400030a.

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5

Mukherjee, Herschel, Nolan T. McDougal, Scott C. Virgil, and Brian M. Stoltz. "A Catalytic, Asymmetric Formal Synthesis of (+)-Hamigeran B." Organic Letters 13, no. 5 (2011): 825–27. http://dx.doi.org/10.1021/ol102669z.

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6

Trost, Barry M., Carole Pissot-Soldermann, and Irwin Chen. "A Short and Concise Asymmetric Synthesis of Hamigeran B." Chemistry - A European Journal 11, no. 3 (2005): 951–59. http://dx.doi.org/10.1002/chem.200400558.

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7

Li, Ruo-Xin, Rui Han, Guo-Jie Wu, Fu-She Han, and Jin-Ming Gao. "Synthesis and Biological Evaluation of Diversified Hamigeran B Analogs as Neuroinflammatory Inhibitors and Neurite Outgrowth Stimulators." Marine Drugs 18, no. 6 (2020): 306. http://dx.doi.org/10.3390/md18060306.

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Abstract:

We describe the efficient synthesis of a series of new simplified hamigeran B and 1-hydroxy-9-epi-hamigeran B norditerpenoid analogs (23 new members in all), structurally related to cyathane diterpenoid scaffold, and their anti-neuroinflammatory and neurite outgrowth-stimulating (neurotrophic) activity. Compounds 9a, 9h, 9o, and 9q exhibited moderate nerve growth factor (NGF)-mediated neurite-outgrowth promoting effects in PC-12 cells at the concentration of 20 μm. Compounds 9b, 9c, 9o, 9q, and 9t showed significant nitric oxide (NO) production inhibition in lipopolysaccharide (LPS)-activated

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8

Cao, Bao-Chen, Guo-Jie Wu, Fang Yu, Yu-Peng He, and Fu-She Han. "A Total Synthesis of (−)-Hamigeran B and (−)-4-Bromohamigeran B." Organic Letters 20, no. 12 (2018): 3687–90. http://dx.doi.org/10.1021/acs.orglett.8b01490.

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9

Jiang, Biao, Ming-ming Li, Ping Xing, and Zuo-gang Huang. "ChemInform Abstract: A Concise Formal Synthesis of (-)-Hamigeran B (XIV)." ChemInform 44, no. 28 (2013): no. http://dx.doi.org/10.1002/chin.201328176.

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10

Sperry, Jeffrey B., and Dennis L. Wright. "Synthesis of the hamigeran skeleton through an electro-oxidative coupling reaction." Tetrahedron Letters 46, no. 3 (2005): 411–14. http://dx.doi.org/10.1016/j.tetlet.2004.11.108.

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