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Volumn 20, Issue 41, 2014, Pages 13203-13209

C(sp3)-H Activation without a Directing Group: Regioselective Synthesis of N-Ylide or N-Heterocyclic Carbene Complexes Controlled by the Choice of Metal and Ligand

Author keywords

C H activation; cooperative effects; iridium; synthetic methods; ylides

Indexed keywords

ACTIVATION ANALYSIS; CHELATION; CHEMICAL ACTIVATION; CHLORINE COMPOUNDS; DENSITY FUNCTIONAL THEORY; ESTERS; IRIDIUM; LIGANDS; ORGANIC COMPOUNDS; REGIOSELECTIVITY; SYNTHESIS (CHEMICAL);

EID: 84941081490     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201403860     Document Type: Article
Times cited : (14)

References (73)
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    • For examples of allylic C-H activation, see:
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    • For examples of benzylic C-H activation, see
    • For examples of benzylic C-H activation, see:
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    • 3)-H bonds in carbonyl compounds are well established, these reactions typically differ from our definition by employing a strong base, such as an alkali metal amide or alkoxide, to generate a stoichiometric alkali metal enolate; for relevant reviews, see
    • 3)-H bonds in carbonyl compounds are well established, these reactions typically differ from our definition by employing a strong base, such as an alkali metal amide or alkoxide, to generate a stoichiometric alkali metal enolate; for relevant reviews, see:
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    • For examples α-C-H activation via oxidative addition, see:
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    • 2] at elevated temperatures, see:
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    • For bidentate carbene/N-ylide complexes, see
    • For bidentate carbene/N-ylide complexes, see:
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    • For examples of metal or ligand control of selectivity in C-H activation, see
    • For examples of metal or ligand control of selectivity in C-H activation, see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.