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Volumn 135, Issue 30, 2013, Pages 10986-10989

Total synthesis of (+)-trienomycins A and F via C-C bond-forming hydrogenation and transfer hydrogenation

Author keywords

[No Author keywords available]

Indexed keywords

BOND FORMING; ENANTIOSELECTIVE; LINEAR SEQUENCE; MACROCYCLES; REDUCTIVE COUPLINGS; RING CLOSING METATHESIS; TOTAL SYNTHESIS; TRANSFER HYDROGENATIONS;

EID: 84881075774     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja4061273     Document Type: Article
Times cited : (42)

References (78)
  • 61
    • 5644254180 scopus 로고    scopus 로고
    • Screening a wide range of ligands showed that RuPhos is uniquely effective in the present B -alkyl Suzuki cross-coupling. See: Milne, J. E.; Buchwald, S. L. J. Am. Chem. Soc. 2004, 126, 3028
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 3028
    • Milne, J.E.1    Buchwald, S.L.2
  • 78
    • 0004938188 scopus 로고
    • "The ideal synthesis creates a complex skeleton... in a sequence only of successive construction reactions involving no intermediary refunctionalizations, and leading directly to the structure of the target, not only its skeleton but also its correctly placed functionality." Hendrickson, J. B. J. Am. Chem. Soc. 1975, 97, 5784
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 5784
    • Hendrickson, J.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.