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Volumn 276, Issue 1-2, 2007, Pages 235-243

Tailoring the ligand structure to the reagent in the mandelamide-Ti(IV) catalyzed enantioselective addition of dimethyl- and diethylzinc to aldehydes

Author keywords

Alkylation; Asymmetric catalysis; Chiral alcohols; Dialkylzinc; Organometallics; Titanium

Indexed keywords

ALDEHYDES; ALKYLATION; AMIDES; CATALYSIS; ENANTIOSELECTIVITY; MOLECULAR STRUCTURE; ORGANOMETALLICS; TITANIUM COMPOUNDS;

EID: 34548530582     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2007.07.019     Document Type: Article
Times cited : (22)

References (91)
  • 1
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    • For reviews.
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    • Pu L. Tetrahedron 59 (2003) 9873-9886
    • (2003) Tetrahedron , vol.59 , pp. 9873-9886
    • Pu, L.1
  • 41
    • 34548526583 scopus 로고    scopus 로고
    • For some recent examples see:
  • 50
    • 34548533283 scopus 로고    scopus 로고
    • For some examples on the less studied addition of di-N-butylzinc and other organozinc reagents see:
  • 69
    • 34548527174 scopus 로고    scopus 로고
    • α-Hydroxyacids can be prepared by diazotation of α-aminoacids.
  • 73
    • 33645917991 scopus 로고    scopus 로고
    • Simultaneously to the development of this work we found that mandelamides catalyze the addition of dimethyzinc to α-ketoesters with good yields and enantioselectivities: G. Blay, I. Fernández, A. Marco-Aleixandre, J. R. Pedro, Org. Lett. 8 (2006) 1287-1290.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.