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Volumn 15, Issue 3, 2009, Pages 697-709

Asymmetric claisen rearrangements on chiral vinyl sulfoxides

Author keywords

Diastereoselectivity; Rearrangement; Sulfides; Sulfones; Sulfoxides

Indexed keywords

ALDEHYDES; INFRARED SPECTROGRAPHS; KETONES; ORGANIC COMPOUNDS; SULFUR COMPOUNDS;

EID: 58449112981     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200801680     Document Type: Article
Times cited : (14)

References (96)
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    • After extensive experimentation, the acetate derived from 3b did not provide the desired silyl ketene acetal involved in the Ireland-Claisen rearrangement. Coordination of the metallated oxygen atom of the enolate derived from 3b and the sulfinyl group could explain the lack of reactivity found.
    • After extensive experimentation, the acetate derived from 3b did not provide the desired silyl ketene acetal involved in the Ireland-Claisen rearrangement. Coordination of the metallated oxygen atom of the enolate derived from 3b and the sulfinyl group could explain the lack of reactivity found.
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    • For a detailed analysis see the Supporting Information
    • For a detailed analysis see the Supporting Information.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.