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tert-BuOK-mediated carbanion―yne intramolecular cyclization: synthesis of 2-substituted 3-benzylbenzofurans

Author
CHEN, Po-Yuan1 ; WANG, Tzu-Pin1 ; HUANG, Keng-Shiang2 ; KAO, Chai-Lin1 ; TSAI, Jui-Chi1 ; WANG, Eng-Chi1
[1] Department of Medicinal & Applied Chemistry, Kaohsiung Medical University, Kaohsiung 807, Taiwan, Province of China
[2] School of Chinese Medicine for Post-Baccalaureate, I-Shou University, Kaohsiung 82445, Taiwan, Province of China
Source

Tetrahedron (Oxford. Print). 2011, Vol 67, Num 48 ; 9226, 9291-9297 [8 p.]

CODEN
TETRAB
ISSN
0040-4020
Scientific domain
Organic chemistry
Publisher
Elsevier, Kidlington
Publication country
United Kingdom
Document type
Article
Language
English
Author keyword
2-Substituted 3-benzylbenzofurans 5-exo-dig Cyclization Carbanion-yne intramolecular cyclization Sonogashira reaction o-lodophenol
Keyword (fr)
Alkylation Carbanion Composé acétylénique Cyclisation Dérivé du benzofurane Hétérocycle oxygène Réaction intramoléculaire Régiosélectivité Stéréoisomère exo Synthèse chimique Copulation Sonogashira Couplage de Sonogashira Potassium t-butanolate
Keyword (en)
Alkylation Carbanion Acetylenic compound Cyclization Benzofuran derivatives Oxygen heterocycle Intramolecular reaction Regioselectivity Exo stereoisomer Chemical synthesis Sonogashira coupling Potassium t-butanolate
Keyword (es)
Alquilación Carbanión Compuesto acetilénico Ciclización Heterociclo oxígeno Reacción intramolecular Regioselectividad Estereoisómero exo Síntesis química
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
25489317

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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