Synthesis of Seven-Membered Cross-Conjugated Cyclic Trienes by 8π Electrocyclic Reaction.


Journal

Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393

Informations de publication

Date de publication:
19 11 2021
Historique:
pubmed: 30 10 2021
medline: 30 10 2021
entrez: 29 10 2021
Statut: ppublish

Résumé

A method for the synthesis of 3-methylene-1,4-cycloheptadiene derivatives via an 8π electrocyclization reaction was developed. The triene substrate bearing a phosphate or carbamate group was prepared from γ,δ-unsaturated esters and α,β-unsaturated aldehydes in four steps. Upon treatment with NaHMDS or KHMDS, the substrate formed a heptatrienyl anion, which underwent electrocyclization and subsequent β-elimination of the leaving group. The product could be converted into a tropylium salt in two steps.

Identifiants

pubmed: 34714079
doi: 10.1021/acs.orglett.1c03383
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

8878-8882

Auteurs

Ranmaru Kato (R)

Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo 060-0810, Japan.

Hiroki Saito (H)

Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo 060-0810, Japan.

Shoko Uda (S)

Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo 060-0810, Japan.

Daisuke Domon (D)

Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo 060-0810, Japan.

Kazutada Ikeuchi (K)

Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan.

Takahiro Suzuki (T)

Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan.

Keiji Tanino (K)

Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan.

Classifications MeSH