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Volumn 50, Issue 22, 2011, Pages 5018-5022

Organocatalysis and C-H activation meet radical- and electron-transfer reactions

Author keywords

aryl radicals; C H activation; homolytic radical substitutions; organocatalysis; radical anions

Indexed keywords

ARYL RADICALS; C-H ACTIVATION; HOMOLYTIC RADICAL SUBSTITUTIONS; ORGANOCATALYSIS; RADICAL ANIONS;

EID: 79956102547     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201101597     Document Type: Article
Times cited : (428)

References (54)
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    • Similar to the authors, we use "organocatalysis" here in the broad sense. In other words, it does not have to be "asymmetric" to be organocatalysis
    • Similar to the authors, we use "organocatalysis" here in the broad sense. In other words, it does not have to be "asymmetric" to be organocatalysis.
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    • For example, we conducted additions of 4-iodoanisole to two substituted arenes under the conditions used in Ref. [14] and obtained ratios very similar to those reported by Shi and co-workers in Ref. [1]: 1) addition to toluene: according to Ref. [1], 58 % yield, o/m/p, 57:23:20; according to Ref. [14], 27 %, 64:23:13; 2) addition to anisole: according to Ref. [1], 70 %, 63:23:14; according to Ref. [14], 52 %, 74:13:13
    • For example, we conducted additions of 4-iodoanisole to two substituted arenes under the conditions used in Ref. [14] and obtained ratios very similar to those reported by Shi and co-workers in Ref. [1]: 1) addition to toluene: according to Ref. [1], 58 % yield, o/m/p, 57:23:20; according to Ref. [14], 27 %, 64:23:13; 2) addition to anisole: according to Ref. [1], 70 %, 63:23:14; according to Ref. [14], 52 %, 74:13:13.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.