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Volumn 137, Issue 30, 2015, Pages 9539-9542

Intramolecular tsujitrost-type allylation of carboxylic acids: Asymmetric synthesis of highly π-allyl donative lactones

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLATION; CATALYSIS; ESTERS; PYRIDINE;

EID: 84939131475     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.5b05786     Document Type: Article
Times cited : (41)

References (48)
  • 10
    • 84859621571 scopus 로고    scopus 로고
    • For some examples for the related halo- or selenolactonization, see: (c) Dobish, M. C.; Johnston, J. N. J. Am. Chem. Soc. 2012, 134, 6068-6071.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 6068-6071
    • Dobish, M.C.1    Johnston, J.N.2
  • 19
    • 14844297329 scopus 로고    scopus 로고
    • For other asymmetric catalyses producing chiral allyl esters, see: (c) Kirsch, S. F.; Overman, L. E. J. Am. Chem. Soc. 2005, 127, 2866-2867.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 2866-2867
    • Kirsch, S.F.1    Overman, L.E.2
  • 27
  • 29
  • 41
    • 1642576013 scopus 로고    scopus 로고
    • The D-labeled substrate was prepared on the basis of asymmetric (n-C4H9)3SnD reduction using Ti(Oi-C3H7)4/(S)-BINOL complex.18 For the first report on analysis of the D-contained alkene stereochemistry in mechanistic study on a Mo catalysis, see: (a) Lloyd-Jones, G. C.; Krska, S. W.; Hughes, D. L.; Gouriou, L.; Bonnet, V. D.; Jack, K.; Sun, Y.; Reamer, R. A. J. Am. Chem. Soc. 2004, 126, 702-703.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 702-703
    • Lloyd-Jones, G.C.1    Krska, S.W.2    Hughes, D.L.3    Gouriou, L.4    Bonnet, V.D.5    Jack, K.6    Sun, Y.7    Reamer, R.A.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.