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Volumn 134, Issue 41, 2012, Pages 17083-17093

Studies toward the unique pederin family member psymberin: Full structure elucidation, two alternative total syntheses, and analogs

Author keywords

[No Author keywords available]

Indexed keywords

ARYL FRAGMENTS; BIOLOGICAL STUDIES; CHEMICAL BIOLOGY; CONVERGENT APPROACH; DIASTEREOSELECTIVE; ENANTIOSELECTIVE; FLEXIBLE STRATEGIES; LINEAR SEQUENCE; NEOPENTYL GLYCOL; ONE-POT PROCEDURES; PEDERIN; RELATED COMPOUNDS; SECOND GENERATION; SECOND-GENERATION SYNTHESIS; SONOGASHIRA COUPLING; STRUCTURE ELUCIDATION; SYNTHETIC APPROACH; TETRAHYDROPYRAN; TOTAL SYNTHESIS;

EID: 84867553335     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja3057612     Document Type: Article
Times cited : (68)

References (92)
  • 6
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    • Mulzer, J. Bohlmann, R. Ernst Schering Research Foundation Workshop 32; Springer: New York
    • Narquizian, R.; Kocienski, P. J. In The Role of Natural Products in Drug Discovery; Mulzer, J.; Bohlmann, R., Eds.; Ernst Schering Research Foundation Workshop 32; Springer: New York, 2000; pp 25-56.
    • (2000) The Role of Natural Products in Drug Discovery , pp. 25-56
    • Narquizian, R.1    Kocienski, P.J.2
  • 8
    • 84875084698 scopus 로고    scopus 로고
    • For a complete listing of pederin related natural products, see the Supporting Information of ref 1
    • For a complete listing of pederin related natural products, see the Supporting Information of ref 1.
  • 57
    • 46549103031 scopus 로고
    • We have not been able to determine if this represents a kinetic or thermodynamic ratio as all attempts to equilibrate the individual N -acylaminal diastereomers led to decomposition. We favor the interpretation of kinetic product formation under the reductive basic reaction conditions because N -acylaminals are known to equilibrate only under acidic conditions. For a review, see: Speckamp, W. N.; Hiemstra, H. Tetrahedron 1985, 41, 4367
    • (1985) Tetrahedron , vol.41 , pp. 4367
    • Speckamp, W.N.1    Hiemstra, H.2
  • 58
    • 0001601216 scopus 로고
    • 2) gave incomplete conversion, providing the amide in 50% isolated yield. For a reference, see: Venit, J. J.; DiPierro, M.; Magnus, P. J. Org. Chem. 1989, 54, 4298
    • (1989) J. Org. Chem. , vol.54 , pp. 4298
    • Venit, J.J.1    Dipierro, M.2    Magnus, P.3
  • 61
    • 84867535597 scopus 로고    scopus 로고
    • Org. Synth. 2002, 79, 59.
    • (2002) Org. Synth. , vol.79 , pp. 59


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.