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Volumn 63, Issue 45, 2007, Pages 10930-10938

Conjugate reduction of α,β-unsaturated esters and amides with tributyltin hydride in the presence of magnesium bromide diethyl etherate

Author keywords

, Unsaturated esters and amides; Conjugate reduction; Lewis acid; Tributyltin hydride

Indexed keywords

ACRYLIC ACID; ALPHA,BETA UNSATURATED ESTER; AMIDE; DIETHYL ITACONATE; ESTER DERIVATIVE; HALIDE; MAGNESIUM BROMIDE DIETHYL ETHERATE; N CROTONYLCAMPHORSULTAM; PACTOLACTONE ESTER; TRIBUTYLTIN HYDRIDE; UNCLASSIFIED DRUG;

EID: 34648835362     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.08.059     Document Type: Article
Times cited : (5)

References (50)
  • 18
    • 1242272908 scopus 로고    scopus 로고
    • A part of the results in this article has been reported as a preliminary letter:
    • A part of the results in this article has been reported as a preliminary letter:. Hirasawa S., Nagano H., and Kameda K. Tetrahedron Lett. 45 (2004) 2207-2209
    • (2004) Tetrahedron Lett. , vol.45 , pp. 2207-2209
    • Hirasawa, S.1    Nagano, H.2    Kameda, K.3
  • 19
    • 34648829465 scopus 로고    scopus 로고
    • It has been reported that aryl acrylates react much faster than their alkyl counterparts in the Baylis-Hillman reactions.
  • 23
    • 1642306315 scopus 로고    scopus 로고
    • For the chelation-controlled stereoselective catalytic hydrogenation of γ-hydroxy-α-methylene carboxylic acid esters, see:
    • For the chelation-controlled stereoselective catalytic hydrogenation of γ-hydroxy-α-methylene carboxylic acid esters, see:. Nagano H., Yokota M., and Iwazaki Y. Tetrahedron Lett. 45 (2004) 3035-3037
    • (2004) Tetrahedron Lett. , vol.45 , pp. 3035-3037
    • Nagano, H.1    Yokota, M.2    Iwazaki, Y.3
  • 24
    • 34648817816 scopus 로고    scopus 로고
    • note
    • No reduction of alkyl acrylates was observed under the reaction conditions.
  • 25
    • 34648814672 scopus 로고    scopus 로고
    • For conjugate reductions of α,β-unsaturated esters with metal hydrides other than tin hydrides, see:
  • 38
    • 0013297136 scopus 로고    scopus 로고
    • and references cited therein
    • Bouzide A. Org. Lett. 4 (2002) 1347-1350 and references cited therein
    • (2002) Org. Lett. , vol.4 , pp. 1347-1350
    • Bouzide, A.1
  • 42
    • 34648820893 scopus 로고    scopus 로고
    • For the reductive elimination reactions of Baylis-Hillman adducts, see:
  • 50
    • 34648820892 scopus 로고    scopus 로고
    • note
    • The chelation-controlled diastereoselective radical addition and reduction reactions of γ-substituted α-methylene-γ-butyrolactams will be reported elsewhere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.