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Volumn 6, Issue 5, 2016, Pages 3381-3386

Silver-Assisted, Iridium-Catalyzed Allylation of Bis[(pinacolato)boryl]methane Allows the Synthesis of Enantioenriched Homoallylic Organoboronic Esters

Author keywords

bis (pinacolato)boryl methane; boronic esters; catalysis; enantioselective allylation; iridium; silver

Indexed keywords

ALLYLATION; CATALYSIS; ENANTIOSELECTIVITY; ESTERS; IRIDIUM; METHANE; SILVER;

EID: 84973575299     PISSN: None     EISSN: 21555435     Source Type: Journal    
DOI: 10.1021/acscatal.6b00719     Document Type: Article
Times cited : (96)

References (107)
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    • Compound 10 is commercially available [from, e.g. Sigma-Aldrich (Catalog No. 794287) and TCI (Catalog No. B4103)]. For the original synthetic method of this compound, see: The Morken group (ref 11h) and the Fu group (ref 11i) have each reported a modified synthesis of this compound
    • Compound 10 is commercially available [from, e.g., Sigma-Aldrich (Catalog No. 794287) and TCI (Catalog No. B4103)]. For the original synthetic method of this compound, see: Matteson, D. S.; Moody, R. J. Organometallics 1982, 1, 20-28. The Morken group (ref 11h) and the Fu group (ref 11i) have each reported a modified synthesis of this compound. 10.1021/om00061a005
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    • In a recent study by the Carreira group, N,N-dialkylhydrozones was used as a formyl anion equivalent in Ir-catalyzed AAS reactions. See
    • In a recent study by the Carreira group, N,N-dialkylhydrozones was used as a formyl anion equivalent in Ir-catalyzed AAS reactions. See: Breitler, S.; Carreira, E. M. J. Am. Chem. Soc. 2015, 137, 5296-5299 10.1021/jacs.5b01951
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    • For a review on kinetic resolution, see: (a)
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    • For a related kinetic resolution process, see: ref 16
    • For a related kinetic resolution process, see: ref 16.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.