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Volumn , Issue 12, 2008, Pages 1938-1942

A concise stereoselective total synthesis of herbarumin III

Author keywords

Crimmins aldol reaction; Macrolide; Olefin metathesis; Phytotoxic; Syn reduction

Indexed keywords

OLEFINS;

EID: 46649083430     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1067089     Document Type: Article
Times cited : (37)

References (39)
  • 18
    • 33846576900 scopus 로고    scopus 로고
    • For our few recent contributions on less-than-ten-membered-ring lactones, see: a
    • For our few recent contributions on less-than-ten-membered-ring lactones, see: (a) Sabitha, G.; Yadagiri, K.; Yadav, J. S. Tetrahedron Lett. 2007, 48, 1651.
    • (2007) Tetrahedron Lett , vol.48 , pp. 1651
    • Sabitha, G.1    Yadagiri, K.2    Yadav, J.S.3
  • 23
    • 34548442872 scopus 로고    scopus 로고
    • For ten- and more-than-ten-membered-ring lactones, see: f
    • For ten- and more-than-ten-membered-ring lactones, see: (f) Nagaiah, K.; Sreenu, D.; Rao, R. S.; Yadav, J. S. Tetrahedron Lett. 2007, 48, 7173.
    • (2007) Tetrahedron Lett , vol.48 , pp. 7173
    • Nagaiah, K.1    Sreenu, D.2    Rao, R.S.3    Yadav, J.S.4
  • 29
    • 0034704636 scopus 로고    scopus 로고
    • N-Acetylthiazolidinethione was synthesized by a protocol similar to that given in the following: (a) Crimmins, M. T.; Chaudhary, K. Org. Lett. 2000, 2, 775.
    • N-Acetylthiazolidinethione was synthesized by a protocol similar to that given in the following: (a) Crimmins, M. T.; Chaudhary, K. Org. Lett. 2000, 2, 775.
  • 30
    • 4544234152 scopus 로고    scopus 로고
    • For Crimmins's aldol approach, see: b
    • For Crimmins's aldol approach, see: (b) Hodge, M. B.; Olivo, H. F. Tetrahedron 2004, 60, 9397.
    • (2004) Tetrahedron , vol.60 , pp. 9397
    • Hodge, M.B.1    Olivo, H.F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.