Vilsmeier-Haack reaction of methyl lambertianate and non-sensitized photocyclization of the resulting product

Vilsmeier-Haack reaction of methyl lambertianate and non-sensitized photocyclization of the resulting product Full article

Journal

Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171

Output data

Year: 1995, Volume: 44, Number: 12, Pages: 2412-2414 Pages count : 3 DOI: 10.1007/BF00713615

Tags

diterpenoids; alkylfurans; formylation; intramolecular photocyclization

Authors

Klok D.A. ¹ , Shakirov M.M. ² , Grishko V.V. ² , Raldugin V.A. ²

Affiliations

1	Novosibirsk State University, 2 ul. Pirogova, 630090, Novosibirsk, Russian Federation
2	Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 prosp. Akad. Lavrent'eva, 630090, Novosibirsk, Russian Federation

Vilsmeier-Haack formylation of methyl lambertianate results in its 16-formyl derivative as the predominant product, which readily enters the intramolecular reaction of photochemical [2+2]-cycloaddition in the absence of a sensitizer.

Klok D.A. , Shakirov M.M. , Grishko V.V. , Raldugin V.A.
Vilsmeier-Haack reaction of methyl lambertianate and non-sensitized photocyclization of the resulting product
Russian Chemical Bulletin. 1995. V.44. N12. P.2412-2414. DOI: 10.1007/BF00713615 WOS Scopus РИНЦ OpenAlex

Published print:

Dec 1, 1995

Web of science:	WOS:A1995UE90700033
Scopus:	2-s2.0-21344442117
Elibrary:	31193743
OpenAlex:	W2951328155

DB	Citing
Web of science	5
Scopus	6
Elibrary	6
OpenAlex	4