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

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

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2021, Volume: 31, Number: 5, Pages: 693-695 Pages count : 3 DOI: 10.1016/j.mencom.2021.09.033

Authors

Gurskii Mikhail E. ¹ , Zuev Maxim I. ¹ , Eshtukov Artur V. ² , Cheshkov Dmitry A. ² , Baranin Sergey V. ¹ , Bubnov Yurii N. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation
2	State Scientific Research Institute of Chemistry and Technology of Organoelement Compounds, 105118 Moscow, Russian Federation

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.

Gurskii M.E. , Zuev M.I. , Eshtukov A.V. , Cheshkov D.A. , Baranin S.V. , Bubnov Y.N.
Stereospecific synthesis of aryltetraline lignan analogues using 1,6-bis(dipropylboryl)hexa-2,4-diene
Mendeleev Communications. 2021. V.31. N5. P.693-695. DOI: 10.1016/j.mencom.2021.09.033 WOS Scopus OpenAlex

≡ Web of science:	WOS:000717972600033
≡ Scopus:	2-s2.0-85119493192
≡ OpenAlex:	W3208420972