메뉴 건너뛰기




Volumn 5, Issue 4, 2014, Pages 1442-1448

Highly enantioselective S-H bond insertion cooperatively catalyzed by dirhodium complexes and chiral spiro phosphoric acids

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION BARRIERS; COOPERATIVE CATALYSIS; DIRHODIUM COMPLEX; HIGH ENANTIOSELECTIVITY; INSERTION PRODUCTS; REACTION CONDITIONS; SITU FT-IR SPECTROSCOPY; SULFUR-CONTAINING COMPOUNDS;

EID: 84897743008     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c3sc52807c     Document Type: Article
Times cited : (128)

References (65)
  • 2
    • 84897736786 scopus 로고    scopus 로고
    • The table of Top 200 Pharmaceutical Products by Total US Prescriptions in 2011
    • The table of Top 200 Pharmaceutical Products by Total US Prescriptions in 2011, http://www.pharmacytimes.com/publications/issue/2012/July2012/Top-200- Drugs-of-2011
  • 20
    • 84865312995 scopus 로고    scopus 로고
    • for selected examples on highly enantioselective O-H and N-H bond insertion reactions, see
    • S.-F. Zhu Q.-L. Zhou Acc. Chem. Res. 2012 45 1365
    • (2012) Acc. Chem. Res. , vol.45 , pp. 1365
    • Zhu, S.-F.1    Zhou, Q.-L.2
  • 32
    • 0000100584 scopus 로고    scopus 로고
    • For the asymmetric N-H bond insertion cooperatively catalyzed by rhodium and chiral spiro phosphoric acids, see
    • M. P. Doyle D. C. Forbes Chem. Rev. 1998 98 911
    • (1998) Chem. Rev. , vol.98 , pp. 911
    • Doyle, M.P.1    Forbes, D.C.2
  • 55
    • 71749112790 scopus 로고    scopus 로고
    • Yu and colleagues have found that the intramolecular [1,2]-proton shift and [1,3]-proton shift are difficult and these are usually catalyzed by a trace amount of water or other protonic solvents/reagents in the reaction systems
    • Y. Liang H.-L. Zhou Z.-X. Yu J. Am. Chem. Soc. 2009 131 17783
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 17783
    • Liang, Y.1    Zhou, H.-L.2    Yu, Z.-X.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.