메뉴 건너뛰기




Volumn , Issue 22, 2004, Pages 2606-2607

Stereoconservative Negishi arylation and alkynylation as an efficient approach to enantiopure 2,2′-diarylated 1,1′-binaphthyls

Author keywords

[No Author keywords available]

Indexed keywords

2,2' DIODO 1,1' BINAPHTHYL; NAPHTHYL GROUP; UNCLASSIFIED DRUG;

EID: 10044253045     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b410185e     Document Type: Article
Times cited : (42)

References (30)
  • 2
    • 0042880949 scopus 로고    scopus 로고
    • (a) Reviews or representative examples: K. Maruoka and T. Ooi, Chem. Rev., 2003, 103, 3013;
    • (2003) Chem. Rev. , vol.103 , pp. 3013
    • Maruoka, K.1    Ooi, T.2
  • 5
    • 0000718373 scopus 로고    scopus 로고
    • (d) L. Pu, Chem. Rev., 1998, 98, 2405;
    • (1998) Chem. Rev. , vol.98 , pp. 2405
    • Pu, L.1
  • 6
    • 0024279870 scopus 로고
    • (e) D. J. Cram, Science, 1988, 240, 760;
    • (1988) Science , vol.240 , pp. 760
    • Cram, D.J.1
  • 24
    • 0001260317 scopus 로고    scopus 로고
    • Emrys Synthesiszer (Biotage AB, Uppsala), for details, see: A. Stadler and C. O. Kappe., J. Comb. Chem., 2001, 3, 624. For a recent review on controlled microwave chemistry, see: C. O. Kappe, Angew. Chem., Int. Ed., 2004, 43, in press.
    • (2001) J. Comb. Chem. , vol.3 , pp. 624
    • Stadler, A.1    Kappe, C.O.2
  • 25
    • 84987632557 scopus 로고    scopus 로고
    • in press
    • Emrys Synthesiszer (Biotage AB, Uppsala), for details, see: A. Stadler and C. O. Kappe., J. Comb. Chem., 2001, 3, 624. For a recent review on controlled microwave chemistry, see: C. O. Kappe, Angew. Chem., Int. Ed., 2004, 43, in press.
    • (2004) Angew. Chem., Int. Ed. , pp. 43
    • Kappe, C.O.1
  • 30
    • 10044222454 scopus 로고    scopus 로고
    • note
    • Enantiopure 3a is commercially available at a price similar to the less reactive 3b. Current supplier: Ivy Chemicals Corporation, wwvv.ivychem.com.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.