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Volumn 49, Issue 32, 2008, Pages 4701-4703

Catalytic enantioselective allylation of aldehydes using β-amido functionalized allylstannanes with chiral In(OTf)3/i-Pr-pybox complexes

Author keywords

Methylene butyrolactone; Amido allylstannane; (S) i Pr pybox; Aldehyde; Catalytic enantioselective allylation; In(OTf)3

Indexed keywords

2,6 BIS[ 4 ISOPROPYLOXAZOLIN 2 YL]PYRIDINE ( I PR PYBOX); ALDEHYDE DERIVATIVE; ALLYL COMPOUND; AMIDE; BETA AMIDO ALLYLTRIBUTYLSTANNANE DERIVATIVE; GAMMA HYDROXY AMIDE DERIVATIVE; PYRIDINE DERIVATIVE;

EID: 45649084700     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.05.123     Document Type: Article
Times cited : (18)

References (45)
  • 1
    • 0041878778 scopus 로고    scopus 로고
    • For a general review, see: and references cited therein.
    • For a general review, see:. Denmark S.E., and Fu J. Chem. Rev. 103 (2003) 2763 and references cited therein.
    • (2003) Chem. Rev. , vol.103 , pp. 2763
    • Denmark, S.E.1    Fu, J.2
  • 23
    • 0000544839 scopus 로고
    • Recently diastereoselective allylation was reported
    • Tanaka K., Yoda H., Isobe Y., and Kaji A. J. Org. Chem. 51 (1986) 1856 Recently diastereoselective allylation was reported
    • (1986) J. Org. Chem. , vol.51 , pp. 1856
    • Tanaka, K.1    Yoda, H.2    Isobe, Y.3    Kaji, A.4
  • 25
    • 15044362616 scopus 로고    scopus 로고
    • For reviews on α-methylene-γ-lactones, see:
    • For reviews on α-methylene-γ-lactones, see:. Bandichhor R., Nosse B., and Reiser O. Top. Curr. Chem. 243 (2005) 43
    • (2005) Top. Curr. Chem. , vol.243 , pp. 43
    • Bandichhor, R.1    Nosse, B.2    Reiser, O.3
  • 41
    • 45649083354 scopus 로고    scopus 로고
    • note
    • A general method for preparation of β-amido allylstannanes was reported in Ref. 2b.
  • 42
    • 45649083010 scopus 로고    scopus 로고
    • note
    • 2+Na: 290.1157, found 290.1128.
  • 43
    • 0342547018 scopus 로고    scopus 로고
    • The absolute configuration of the stereogenic center of 6a was easily determined to be S after derivation to the corresponding α-methylene-γ-butyrolactone 7a as shown below, see: {A figure is presented}
    • The absolute configuration of the stereogenic center of 6a was easily determined to be S after derivation to the corresponding α-methylene-γ-butyrolactone 7a as shown below, see:. Csuk R., Schröder C., Hutter S., and Mohr K. Tetrahedron: Asymmetry 8 (1997) 1411 {A figure is presented}
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 1411
    • Csuk, R.1    Schröder, C.2    Hutter, S.3    Mohr, K.4
  • 44
    • 45549122277 scopus 로고    scopus 로고
    • note
    • 2a after cyclization again to the corresponding lactone 7b as shown below.{A figure is presented}


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.