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Volumn 48, Issue 43, 2009, Pages 8037-8041

Catalytic enantioselective stereoablative alkylation of 3-halooxindoles: Facile access to oxindoles with c3 all-carbon quaternary stereocenters

Author keywords

Alkylation; Asymmetric catalysis; Copper; Enantioselectivity; Umpolung

Indexed keywords

ALKYLATION; CARBON; COPPER;

EID: 70350014973     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200902943     Document Type: Article
Times cited : (186)

References (121)
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    • Consistent with our proposal of an o-azaxylylene intermediate, exposure of N-methyl bromooxindole 16 to our reaction conditions (see Table 2) failed to give any detectable amount of the malonate adduct.
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    • The absolute configuration depicted for all products in Tables 2 and 3 is derived by analogy from the X-ray analysis of 11.
    • The absolute configuration depicted for all products in Tables 2 and 3 is derived by analogy from the X-ray analysis of 11.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.