Stereoselective isomerisations of 4-(3′,5′-dimethoxyphenyl)-2,5-dimethyl-1,3-dioxolanes. Temperature-dependent formation of either isochromanes or dihydroisobenzofurans-Reference-Cited by-同舟云学术

Stereoselective isomerisations of 4-(3′,5′-dimethoxyphenyl)-2,5-dimethyl-1,3-dioxolanes. Temperature-dependent formation of either isochromanes or dihydroisobenzofurans

Published:1996 Issue:18 Volume: Page:2241-2248
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Giles Robin G. F.,Rickards Rodney W.,Senanayake Badra S.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1996/P1/P19960002241

Reference24 articles.

1. The stereoselective formation of naphtho[1,2-c]pyrans, angular analogues of the aphin-derived glucoside B, by an intramolecular version of the Mukaiyama reaction of 4-naphthyldioxolanes

2. Stereoselective syntheses of benzo- and naphtho-pyrans by Lewis acid catalysed isomerisation of aryldioxolanes

3. Synthesis of the aphin-related (±)-7,9-dideoxyquinone A and (±)-7,9-dideoxyquinone A′

4. Naphthopyrans by ring-closure of substituted naphthalenes using potassium t-butoxide in dimethylformamide

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