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Volumn 41, Issue 16, 2000, Pages 2899-2902

Synthesis of alkaloids from amino acids via N-acyliminium ions generated by one-pot radical decarboxylation-oxidation

Author keywords

Alkaloids; Indolizidinone; N acyliminium ion; Nitrogen heterocycles; Radical decarboxylation

Indexed keywords

ALKALOID; AMINO ACID; HETEROCYCLIC NITRO COMPOUND; INDOLIZIDINE ALKALOID; PIPERIDINE; PYRROLIDINE DERIVATIVE; RADICAL;

EID: 0343415173     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)00306-3     Document Type: Article
Times cited : (35)

References (32)
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    • For general reviews on N-acyliminium ions, see: (a)
    • For general reviews on N-acyliminium ions, see: (a) Padwa, A. Chem. Commun. 1998, 1417-1424.
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  • 5
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    • (f) Brossi, A., Ed.; Academic Press: San Diego
    • (f) Hiemstra, H.; Speckamp, W. N. In The Alkaloids; Brossi, A., Ed.; Academic Press: San Diego, 1988; Vol. 32, p. 271.
    • (1988) In the Alkaloids , vol.32 , pp. 271
    • Hiemstra, H.1    Speckamp, W.N.2
  • 17
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    • Reviews on electroorganic synthesis: (a)
    • Reviews on electroorganic synthesis: (a) Utley, J. Chem. Soc. Rev. 1997, 157-167.
    • (1997) Chem. Soc. Rev. , pp. 157-167
    • Utley, J.1
  • 21
    • 0342506442 scopus 로고    scopus 로고
    • We have noticed that an acetate from the reagent (DIB) reacts with oxycarbenium ion intermediates during the photolysis of carbohydrates: (a)
    • We have noticed that an acetate from the reagent (DIB) reacts with oxycarbenium ion intermediates during the photolysis of carbohydrates: (a) Francisco, C. G.; González, C. C.; Suárez, E. Tetrahedron Lett. 1997, 38, 4141-4144.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 4141-4144
    • Francisco, C.G.1    González, C.C.2    Suárez, E.3
  • 23
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    • The stereochemistry of 3a was determined on the basis of its spectroscopic data, including irradiations and 2D-experiments. For a similar result, see:
    • The stereochemistry of 3a was determined on the basis of its spectroscopic data, including irradiations and 2D-experiments. For a similar result, see: Renaud, P.; Seebach, D. Helv. Chim. Acta 1986, 69, 1704-1710.
    • (1986) Helv. Chim. Acta , vol.69 , pp. 1704-1710
    • Renaud, P.1    Seebach, D.2
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    • (c) and references cited therein
    • (c) Michael, J. P. Nat. Prod. Rep. 1998, 571-594 and references cited therein.
    • (1998) Nat. Prod. Rep. , pp. 571-594
    • Michael, J.P.1
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    • For a review of trialkylsilyloxyfurans, see:
    • For a review of trialkylsilyloxyfurans, see: Casiraghi, G.; Rassu, G. Synthesis 1995, 607-626.
    • (1995) Synthesis , pp. 607-626
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  • 31
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    • For interesting reviews with related strategies, see: (b)
    • For interesting reviews with related strategies, see: (b) Hanessian, S. Tetrahedron 1997, 53, 12789-12854.
    • (1997) Tetrahedron , vol.53 , pp. 12789-12854
    • Hanessian, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.