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Showing papers on "Benzopyrans published in 1985"


Journal ArticleDOI
TL;DR: The ortho-iodoaryl allyl ethers derived from 1 via the aromatic directed metalation protocol, undergo tributyl tin hydride-induced heteroring annelation to lead to unusually substituted benzofuran (3) and benzopyran, and furopyridine derivatives (Table).

69 citations



Journal ArticleDOI
TL;DR: In this paper, a partir des vinyl-2-and ethynyl-2 cyclohexanols et des chloromethyl methyl ether ou ethyl vinyl ether via cyclisation en presence of TiCl 4 des [methoxy-2' ethyl (ou ethyl) R] acetals des formaldehyde and acetaldehyde (R=vinyl ou E-cyclohexyl)
Abstract: Synthese des composes du titre et de leurs derives methyl-2 a partir des vinyl-2- et ethynyl-2 cyclohexanols et des chloromethyl methyl ether ou ethyl vinyl ether via la cyclisation en presence de TiCl 4 des [methoxy-2' ethyl (ou ethyl) R] acetals des formaldehyde et acetaldehyde (R=vinyl ou ethynyl-2 cyclohexyl)

21 citations


Journal ArticleDOI
TL;DR: The accumulation of benzopyrans and benzofurans supports an arrangement of the tribes of the Asteraceae into two groups as suggested recently based on morphological characters.
Abstract: Benzopyrans (chromenes) and benzofurans are characteristic natural products of theAsteraceae and are found together with their biogenetic precursors primarily in the tribesAnthemideae, Astereae, Eupatorieae, Heliantheae, Inuleae, andSenecioneae. The accumulation of benzopyrans and benzofurans supports an arrangement of the tribes of theAsteraceae into two groups as suggested recently based on morphological characters. The methods for analysing this class of natural products are demonstrated with the American genusEncelia. Experiments on the localization of benzopyrans and benzofurans inEncelia species indicate that these compounds are stored in resin ducts. Several benzopyrans and benzofurans are biologically active and are repellent as well as toxic towards herbivorous insects. Experiments on structure — activity relationships indicate the biological activities as being influenced by the heterocycle (pyranvs. furan) as well as by the substituents of the aromatic ring. In addition, several tested compounds showed phototoxic activities.

16 citations


Journal ArticleDOI
TL;DR: In this article, a series of A-ring heterocyclic analogues of tetrahydrocannabinol were investigated, and they were functionalized by formylation with base and ethyl formate to give 6a and 6b.

13 citations


Patent
21 Mar 1985
TL;DR: Novel substituted 4-hydroxy-benzopyrans of the formula "STR1" in which X is a single bond can have various meanings, or pharmaceutically acceptable addition salts thereof, which are active on the circulation system as mentioned in this paper.
Abstract: Novel substituted 4-hydroxy-benzopyrans of the formula ##STR1## in which X is a single bond, ##STR2## and the other radicals can have various meanings, or pharmaceutically acceptable addition salts thereof, which are active on the circulation system.

9 citations


Patent
25 Mar 1985
TL;DR: Substituted benzopyrans of the formula "STR1" can have various meanings, or pharmaceutically acceptable addition salts thereof, which possess anti-hypertensive activity.
Abstract: Substituted benzopyrans of the formula ##STR1## in which --A-- is a single or double bond, X is a direct bond, optionally substituted methylene, oxygen or optionally substituted --NH--, and the various other radicals can have various meanings, or pharmaceutically acceptable addition salts thereof, which possess anti-hypertensive activity.

8 citations



Patent
28 Jan 1985
TL;DR: In this article, the substituents, R5 -R8 and EA are defined in the specification, and these compounds are useful as anti-asthmatic agents; however, they are not suitable for use in the treatment of cancer.
Abstract: There are provided benzopyrans of formula I, ##STR1## wherein the substituents, R5 -R8 and EA are as defined in the specification. These compounds are useful as anti-asthmatic agents.

6 citations


Journal ArticleDOI
TL;DR: In this paper, the condensation of 4-hydroxy-2H-1-benzopyran-2-ones with benzoin in the presence of p-toluene sulphonic acid is described.

5 citations


Patent
18 Mar 1985
TL;DR: In this article, a substitution of substituted benzopy-rane of the formula I in which A, R 1 to R 16 and X have the meanings given in the description, to several processes for their preparation and their use in medicaments, especially in circulation-influencing agents.
Abstract: Die vorliegende Erfindung betrifft substituierte Benzopy- rane der Formel I The present invention relates to substituted Benzopy- rane of the formula I in welcher A, R 1 bis R 16 und X die in der Beschreibung angegebene Bedeutung haben, mehrere Verfahren zu ihrer Herstellung sowie ihre Verwendung in Arzneimitteln, insbesondere in kreislaufbeeinflussenden Mitteln. in which A, R 1 to R 16 and X have the meanings given in the description, to several processes for their preparation and their use in medicaments, especially in circulation-influencing agents.

Patent
26 Aug 1985
TL;DR: There are provided benzopyrans of formula I, wherein the substituents, R5-R8 and EA are as defined in the specification as discussed by the authors.These compounds are useful as anti-asthmatic agents.
Abstract: There are provided benzopyrans of formula I, wherein the substituents, R5-R8 and EA are as defined in the specification. These compounds are useful as anti-asthmatic agents.


Patent
09 Nov 1985
TL;DR: Substituted benzopyrans of the formula in which -A- is a single or double bond, X is a direct bond, optionally substituted methylene, oxygen or optionally substituted -NH-, and the various other radicals can have various meanings, or pharmaceutically acceptable addition salts thereof, which possess anti-hypertensive activity.
Abstract: Substituted benzopyrans of the formula in which -A- is a single or double bond, X is a direct bond, optionally substituted methylene, oxygen or optionally substituted -NH-, and the various other radicals can have various meanings, or pharmaceutically acceptable addition salts thereof, which possess anti-hypertensive activity.