Acid-promoted cycloisomerizations of phenylallenes bearing acetalic functions at the ortho position: a stereocontrolled entry to indeno-fused dioxepanes, dioxocanes and thioanalogues-Reference-Cited by-同舟云学术

Acid-promoted cycloisomerizations of phenylallenes bearing acetalic functions at the ortho position: a stereocontrolled entry to indeno-fused dioxepanes, dioxocanes and thioanalogues

Published:2015 Issue:31 Volume:13 Page:8420-8424
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Marin-Luna Marta¹²³⁴⁵,Vidal Angel¹²³⁴⁵,Bautista Delia⁶²⁴⁵⁷,Orenes Raul-Angel⁶²⁴⁵⁷,Alajarin Mateo¹²³⁴⁵

Affiliation:

1. Departamento de Química Orgánica

2. Universidad de Murcia

3. Facultad de Química

4. Regional Campus of International Excellence “Campus Mare Nostrum”

5. 30100 Murcia

6. Servicio Universitario de Instrumentación Científica

7. Spain

Abstract

Two different approaches convert ortho acetal-substituted phenylallenes into several classes of indeno-fused heterocycles.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB00897B

Reference40 articles.

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2. Acyclic stereoselection. 52. On the mechanism of Lewis acid mediated nucleophilic substitution reactions of acetals

3. Studies on the mechanism and origin of stereoselective opening of chiral dioxane acetals

4. Evidence for an Oxocarbenium Ion Intermediate in Lewis Acid Mediated Reactions of Acyclic Acetals

5. Asymmetric Nucleophilic Substitution of Acetals

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