메뉴 건너뛰기




Volumn , Issue 4, 2006, Pages 409-411

Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL COMPOUND; COPPER; GRIGNARD REAGENT; REAGENT; UNCLASSIFIED DRUG;

EID: 33645450637     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b513887f     Document Type: Article
Times cited : (91)

References (42)
  • 2
    • 0000687774 scopus 로고    scopus 로고
    • Allylic Substitution Reactions, ed.
    • E. N. Jacobsen, A. Pflatz and H. Yamamoto, Springer-Verlag, Berlin, Germany, pp. 833-884 Mo:
    • A. Pfaltz and M. Lautens, in Allylic Substitution Reactions, ed., E. N. Jacobsen, A. Pflatz and H. Yamamoto,, Comprehensive Asymmetric Catalysis I-III; Springer-Verlag, Berlin, Germany, 1999, Vol. II, pp. 833-884
    • (1999) Comprehensive Asymmetric Catalysis I-III;
    • Pfaltz, A.1    Lautens In, M.2
  • 34
    • 33645451167 scopus 로고    scopus 로고
    • 2Zn or MeMgX reagents. See ref. 9b and references cited therein
    • 2Zn or MeMgX reagents. See ref. 9b and references cited therein
  • 36
    • 33645460959 scopus 로고    scopus 로고
    • 2Me) tested under these conditions provided lower conversions and/or selectivities
    • 2Me) tested under these conditions provided lower conversions and/or selectivities
  • 38
    • 33645456637 scopus 로고    scopus 로고
    • 6, CuCl), solvents, or EtMgCl instead of EtMgBr provided the same selectivities. See ESI for more details
    • 6, CuCl), solvents, or EtMgCl instead of EtMgBr provided the same selectivities. See ESI for more details
  • 39
    • 33645451540 scopus 로고    scopus 로고
    • To the best of our knowledge, these are the highest selectivities reported so far for the substitution with a methyl group in this kind of allylic bromides
    • To the best of our knowledge, these are the highest selectivities reported so far for the substitution with a methyl group in this kind of allylic bromides
  • 40
    • 33645449651 scopus 로고    scopus 로고
    • The application of this methodology for the synthesis of relevant natural products is currently underway
    • The application of this methodology for the synthesis of relevant natural products is currently underway
  • 42
    • 33645452851 scopus 로고    scopus 로고
    • The conjugate addition of EtMgBr to (S)-6 using racemic-1b led to an 84 : 16 mixture of 7 and 8, indicating a strong preference for the formation of the 1,2-anti product
    • The conjugate addition of EtMgBr to (S)-6 using racemic-1b led to an 84 : 16 mixture of 7 and 8, indicating a strong preference for the formation of the 1,2-anti product


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.