Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 2002, 67, 55-74
https://doi.org/10.1135/cccc20020055

Synthesis of Methoxynor Polyisoprenoid Alcohols by Alkylation of (3-Methoxyallyl)lithium Reagents

Qingwu Jin and Robert M. Coates*

Department of Chemistry, Roger Adams Laboratory, Box 40-5, University of Illinois, 600 South Mathews Avenue, Urbana, IL 61801, U.S.A.

Crossref Cited-by Linking

  • Harms Vanessa, Kirschning Andreas, Dickschat Jeroen S.: Nature-driven approaches to non-natural terpene analogues. Nat. Prod. Rep. 2020, 37, 1080. <https://doi.org/10.1039/C9NP00055K>
  • Romano Ciro, Mazet ClĂ©ment: Multicatalytic Stereoselective Synthesis of Highly Substituted Alkenes by Sequential Isomerization/Cross-Coupling Reactions. J. Am. Chem. Soc. 2018, 140, 4743. <https://doi.org/10.1021/jacs.8b02134>
  • Zhang Qiong, Huang Lixin, Zhang Caihong, Xie Pujun, Zhang Yaolei, Ding Shasha, Xu Feng: Synthesis and biological activity of polyprenols. Fitoterapia 2015, 106, 184. <https://doi.org/10.1016/j.fitote.2015.09.008>
  • Lauchli Ryan, Rabe Kersten S., Kalbarczyk Karolina Z., Tata Amulya, Heel Thomas, Kitto Rebekah Z., Arnold Frances H.: High-Throughput Screening for Terpene-Synthase-Cyclization Activity and Directed Evolution of a Terpene Synthase. Angew. Chem. 2013, 125, 5681. <https://doi.org/10.1002/ange.201301362>
  • Lauchli Ryan, Rabe Kersten S., Kalbarczyk Karolina Z., Tata Amulya, Heel Thomas, Kitto Rebekah Z., Arnold Frances H.: High-Throughput Screening for Terpene-Synthase-Cyclization Activity and Directed Evolution of a Terpene Synthase. Angew. Chem. Int. Ed. 2013, 52, 5571. <https://doi.org/10.1002/anie.201301362>
  • Jin Qingwu, Coates Robert M.: ChemInform Abstract: Synthesis of Methoxynor Polyisoprenoid Alcohols by Alkylation of (3-Methoxyallyl)lithium Reagents. ChemInform 2010, 33, no. <https://doi.org/10.1002/chin.200237191>
  • Chang Yi-Fan, Liu Chen-Yu, Guo Chih-Wei, Wang Yen-Chih, Fang Jim-Min, Cheng Wei-Chieh: Solid-Phase Organic Synthesis of Polyisoprenoid Alcohols with Traceless Sulfone Linker. J. Org. Chem. 2008, 73, 7197. <https://doi.org/10.1021/jo8010182>