메뉴 건너뛰기




Volumn 10, Issue 41, 2012, Pages 8268-8275

Highly stereoselective modifications of peptides via Pd-catalyzed allylic alkylation of internal peptide amide enolates

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLIC ALKYLATION; DIASTEREOSELECTIVITIES; DRUG MOLECULES; HIGH YIELD; NATURAL PRODUCTS; PEPTIDE AMIDES; STEREO-SELECTIVE;

EID: 84867255611     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob26351c     Document Type: Article
Times cited : (28)

References (43)
  • 18
    • 0001269629 scopus 로고
    • Angew. Chem., Int. Ed. Engl. 1988 27 1624
    • D. Seebach Angew. Chem. 1988 100 1685 1715 Angew. Chem., Int. Ed. Engl. 1988 27 1624
    • (1988) Angew. Chem. , vol.100 , pp. 1685-1715
    • Seebach, D.1
  • 20
    • 0003598101 scopus 로고
    • in, ed. B. Ernst and C. Leumann, Helvetica Chimica Acta/VCH, Basel/Weinheim, 1-178
    • D. Seebach, A. K. Beck and A. Studer, in Modern Synthetic Methods, ed., B. Ernst, and, C. Leumann, Helvetica Chimica Acta/VCH, Basel/Weinheim, 1995, vol. 7, pp. 1-178
    • (1995) Modern Synthetic Methods , vol.7
    • Seebach, D.1    Beck, A.K.2    Studer, A.3
  • 32
    • 38849189437 scopus 로고    scopus 로고
    • Angew. Chem., Int. Ed. 2007 46 4570 4573
    • J. Deska U. Kazmaier Angew. Chem. 2007 119 4654 4657 Angew. Chem., Int. Ed. 2007 46 4570 4573
    • (2007) Angew. Chem. , vol.119 , pp. 4654-4657
    • Deska, J.1    Kazmaier, U.2
  • 37
    • 34250737622 scopus 로고    scopus 로고
    • Angew. Chem., Int. Ed. 2006 45 4855 4858
    • U. Kazmaier J. Deska A. Watzke Angew. Chem. 2006 118 4973 4976 Angew. Chem., Int. Ed. 2006 45 4855 4858
    • (2006) Angew. Chem. , vol.118 , pp. 4973-4976
    • Kazmaier, U.1    Deska, J.2    Watzke, A.3
  • 38
    • 57549101559 scopus 로고    scopus 로고
    • To avoid an epimerization of the proline, the anilide was used at the C-terminus. Deprotonation of the amide under the basic reaction conditions protects the α-position of the proline towards deprotonation. In addition, the aromatic system facilitates the determination of the diastereomeric ratio via HPLC
    • K. Krämer J. Deska C. Hebach U. Kazmaier Org. Biomol. Chem. 2009 7 103 110
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 103-110
    • Krämer, K.1    Deska, J.2    Hebach, C.3    Kazmaier, U.4
  • 39
    • 27544474853 scopus 로고    scopus 로고
    • Angew. Chem., Int. Ed. 2005 44 3303 3306
    • U. Kazmaier T. Lindner Angew. Chem. 2005 117 3368 3371 Angew. Chem., Int. Ed. 2005 44 3303 3306
    • (2005) Angew. Chem. , vol.117 , pp. 3368-3371
    • Kazmaier, U.1    Lindner, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.