메뉴 건너뛰기




Volumn 43, Issue 47, 2004, Pages 6491-6493

Stereospecific, enantioselective allylation of α-hydrazono esters by using allyltrichlorosilanes with BINAP dioxides as neutral-coordinate organocatalysts

Author keywords

Allylation; Amino acids; Asymmetric catalysis; Asymmetric synthesis; Hydrazones

Indexed keywords

REACTION KINETICS; SILICON COMPOUNDS; STEREOCHEMISTRY;

EID: 11144305011     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200461312     Document Type: Article
Times cited : (116)

References (37)
  • 5
    • 0042819676 scopus 로고    scopus 로고
    • T. Hamada, K. Manabe, S. Kobayashi, Angew. Chem. 2003, 115, 4057; Angew. Chem. Int. Ed. 2003, 42, 3927.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 3927
  • 7
    • 0035907033 scopus 로고    scopus 로고
    • For a diastereo- and enantioselective allylation of imines, see: T. Gastner, H. Ishitani, R. Akiyama, S. Kobayashi, Angew. Chem. 2001, 113, 1949; Angew. Chem. Int. Ed. 2001, 40, 1896.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 1896
  • 26
    • 11144293664 scopus 로고    scopus 로고
    • note
    • The stereochemistry of the adducts was tentatively assigned at this stage based on previous data (see ref [3]). It was finally confirmed after converting to D-alloisoleucine (Scheme 1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.