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Volumn 1981, Issue 12, 1981, Pages 2272-2284

A Short Synthesis of (R,R)‐(‐)‐Pyrenophorin from (S)‐Propylene Oxide and a 3‐Pentenoic Acid d5‐Reagent

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EID: 84981407082     PISSN: 01702041     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/jlac.198119811215     Document Type: Article
Times cited : (46)

References (64)
  • 1
    • 84985138888 scopus 로고
    • Syntheses of (+)-(S,S)-(cis-6-Methyltetrahydropyran-2-yl)acetic acid and of (?)-(R,R)-Didesoxy-pyrenophorine Using a New d5-Reagent. Preliminary communication
    • Preliminary Communication of part of this work
    • (1979) Helvetica Chimica Acta , vol.62 , pp. 843
    • Seebach, D.1    Pohmakotr, M.2
  • 2
    • 84981424818 scopus 로고
    • This work was presented by D. Seebach to the Chemische Gesellschaft at Bern on the 16th January, 1980, see
    • (1980) Chimia , vol.33 , pp. 433
  • 3
    • 84981395679 scopus 로고
    • On leave from University of Poona (India), June 1979 to August
    • (1980)
  • 4
    • 84981476673 scopus 로고    scopus 로고
    • Department of Chemistry, Faculty of Sciences, Mohidol University, Rama 6 Road, Bangkok 4, Thailand.
  • 5
    • 84981432050 scopus 로고
    • Part of the Ph. D. thesis of, Universität Gießen
    • (1978)
    • Pohmakotr, M.1
  • 28
    • 84981403622 scopus 로고
    • 6th Int. Symposium on Syntheses in Organic Chemistry, Cambridge, July
    • (1979)
    • Chan, T.H.1
  • 29
    • 84981446055 scopus 로고
    • 1st European Symposium on Organic Chemistry (ESOC 1), Köln, July, Abstract of papers, p.
    • (1979) , pp. 88
    • Zwanenburg, B.1
  • 30
    • 84981395730 scopus 로고    scopus 로고
    • Dep. of Industrial Chemistry, Kyoto University, Kyoto, Japan (unpublished results).
    • Hiyama, T.1
  • 34
    • 0001728892 scopus 로고
    • Methoden der Reaktivitätsumpolung
    • See the recent review article on reactivity umpolung:, Angew. Chem., Int. Ed. Engl
    • (1979) Angewandte Chemie , vol.91 , pp. 259
    • Seebach, D.1
  • 36
    • 84981446057 scopus 로고    scopus 로고
    • For the a,d‐nomenclature of synthetic methodology see ref. 26.
  • 37
    • 84981435381 scopus 로고    scopus 로고
    • Modern Synthetic Methods 1976 and 1980, Conference at Interlaken, Schweizerischer Chemiker Verband. For instance 12 steps from γ‐valerolactone see ref. 14,21.
  • 41
    • 84981394943 scopus 로고    scopus 로고
    • See also references on redox umpolung in our review article mentioned in ref. 26.
  • 43
    • 84981395623 scopus 로고    scopus 로고
    • Eventually, these are ketones allylated in the α‐position.
  • 50
    • 84981395472 scopus 로고    scopus 로고
    • in Stereoselective Synthesis of Natural Products
    • Trost, B.M.1
  • 60
    • 84981378797 scopus 로고
    • Note added in proof (November 9,): Since this paper was submitted, a number of new syntheses of pyrenophorin and vermiculine have been published
    • (1981)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.