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Volumn 133, Issue 22, 2011, Pages 8510-8513

Sulfoxide-mediated α-arylation of carbonyl compounds

Author keywords

[No Author keywords available]

Indexed keywords

ARYLATIONS; ROOM TEMPERATURE;

EID: 79957985277     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja2031882     Document Type: Article
Times cited : (138)

References (78)
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    • The structure of 6aa was unambiguously confirmed by X-ray crystallographic analysis. See the Supporting Information (SI) for details.
    • The structure of 6aa was unambiguously confirmed by X-ray crystallographic analysis. See the Supporting Information (SI) for details.
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    • The configuration of the major isomer was determined by nuclear Overhauser effect (NOE) experiments. See the SI for details.
    • The configuration of the major isomer was determined by nuclear Overhauser effect (NOE) experiments. See the SI for details.
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    • The ratio of 6ad to 7ad was 96/4, as measured by GC. For details of the preparation of an authentic sample of 7ad, see the SI.
    • The ratio of 6ad to 7ad was 96/4, as measured by GC. For details of the preparation of an authentic sample of 7ad, see the SI.
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    • The use of sulfoxide 5f bearing a tert -butyl group led to α-(phenylsulfanyl) ketoester 9 in good yield: See:;;, and references therein
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    • Reference 18.
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    • For examples of alternative synthetically useful manipulations of aromatic sulfanyl substituents (i.e., C-C bond-forming reactions), see refs 18e and 22d.
    • For examples of alternative synthetically useful manipulations of aromatic sulfanyl substituents (i.e., C-C bond-forming reactions), see refs 18e and 22d.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.