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Volumn 17, Issue 15, 2011, Pages 4064-4075

Selective synthesis of β-alkylpyrroles

Author keywords

alkylation; electrophilic aromatic substitution; heterocycles; pyrroles; regioselectivity

Indexed keywords

ALKYLPYRROLES; AROMATICITIES; BIOLOGICALLY ACTIVE COMPOUNDS; ELECTROPHILES; ELECTROPHILIC AROMATIC SUBSTITUTION; ELECTROPHILIC AROMATIC SUBSTITUTIONS; HETEROCYCLES; NATURAL PRODUCTS; ORGANIC MATERIALS; PYRROLE RING; PYRROLES; SELECTIVE SYNTHESIS; STRUCTURAL MOTIFS; SYNTHETIC CHEMISTS;

EID: 79953207362     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002248     Document Type: Article
Times cited : (30)

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    • 3 (10 mol %), a 85:15 mixture of the corresponding β,β′- and α,β′-adducts is produced. No α,α′-isomer is thus formed. Use of pyrroles with bulkier substituents on the nitrogen atom leads to higher selectivity of 41. For further details, see reference [54]
    • 3 (10 mol %), a 85:15 mixture of the corresponding β,β′- and α,β′-adducts is produced. No α,α′-isomer is thus formed. Use of pyrroles with bulkier substituents on the nitrogen atom leads to higher selectivity of 41. For further details, see reference [54].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.