M. E. Gurskii, M. I. Zuev, A. V. Eshtukov, D. A. Cheshkov, S. V. Baranin, Yu. N. Bubnov, “Stereospecific synthesis of aryltetraline lignan analogues using 1,6-bis(dipropylboryl)hexa-2,4-diene”, Mendeleev Commun., 31:5 (2021), 693

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Mendeleev Communications, 2021, Volume 31, Issue 5, Pages 693–695
DOI: https://doi.org/10.1016/j.mencom.2021.09.033 (Mi mendc1025)

Communications

Stereospecific synthesis of aryltetraline lignan analogues using 1,6-bis(dipropylboryl)hexa-2,4-diene

M. E. Gurskii^a, M. I. Zuev^a, A. V. Eshtukov^b, D. A. Cheshkov^b, S. V. Baranin^a, Yu. N. Bubnov^a

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b State Scientific Research Institute of Chemistry and Technology of Organoelement Compounds, Moscow, Russian Federation

Full-text PDF (180 kB)

DOI: https://doi.org/10.1016/j.mencom.2021.09.033

Graphic abstract: Stereospecific synthesis of aryltetraline lignan analogues using 1,6-bis(dipropylboryl)hexa-2,4-diene

Abstract: A novel convenient two-stage synthesis of aryltetraline lignin analogues from aromatic aldehydes and diallyl diboron derivatives on the basis of intramolecular Friedel–Crafts reaction has been developed.

Keywords: allylboration, lignan analogues, Friedel–Crafts reaction, benzylic alcohols, organoboron compounds.

Document Type: Article

Language: English

*Supplementary materials:*
		Supplementary_data_1.pdf	(3.1 Mb)

Citation: M. E. Gurskii, M. I. Zuev, A. V. Eshtukov, D. A. Cheshkov, S. V. Baranin, Yu. N. Bubnov, “Stereospecific synthesis of aryltetraline lignan analogues using 1,6-bis(dipropylboryl)hexa-2,4-diene”, Mendeleev Commun., 31:5 (2021), 693–695

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https://www.mathnet.ru/eng/mendc1025

https://www.mathnet.ru/eng/mendc/v31/i5/p693

Citing articles in Google Scholar: Russian citations, English citations
Related articles in Google Scholar: Russian articles, English articles

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