A new carbon skeleton rearrangement under basic conditions: 2-Hydroxy[3,5-2H2]-benzaldehyde from 2-quinuclidinio[3,5,7-3H2]tropone in concentrated alkali-Reference-Cited by-同舟云学术

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A new carbon skeleton rearrangement under basic conditions: 2-Hydroxy[3,5-2H2]-benzaldehyde from 2-quinuclidinio[3,5,7-3H2]tropone in concentrated alkali

Published:1974-01 Issue:40 Volume:15 Page:3537-3538
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Biggi Gino,Cima Francesco Del,Pietra Francesco

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference12 articles.

1. Pseudoaromatic Compounds. XVI. Part XV: F. Pietra, Chem. Comm., in the press.

2. Seven-membered conjugated carbo- and heterocyclic compounds and their homoconjugated analogs and metal complexes. Synthesis, biosynthesis, structure, and reactivity

3. A new rearrangement of 1-(2-oxocyclohepta-3,5,7-trienyl)-1-azabicyclo[2,2,2]-octanium iodide into m-hydroxybenzaldehyde

4. Reactivity of pseudoaromatic compounds. XI. Base-induced ring contractions of cycloheptatrienones carrying a mobile .alpha. substituent. Available pathways and competition with substitution reactions

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1. ChemInform Abstract: A NEW CARBON SKELETON REARRANGEMENT UNDER BASIC CONDITIONS, 2-HYDROXY-(3,5-(2)H2)-BENZALDEHYDE FROM 2-QUINUCLIDINIO(3,5,7-(3)H2)TROPONE IN CONCENTRATED ALKALI;Chemischer Informationsdienst;1975-01-07

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