A stereoselective synthesis of a C-glycosylated peptoid building block

Tetrahedron Letters

Volumn 39, Issue 3-4, 1998, Pages 253-254

  Dechantsreiter, Michael A ^a   Burkhart, Fred ^a   Kessler, Horst ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOPEPTIDE;

ARTICLE; CHEMICAL MODIFICATION; PEPTIDE SYNTHESIS; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0032518797     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)10566-4     Document Type: Article

References (15)

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8. 1
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12. 12 The ratio of 4a:4b was approximately 1:2. Exclusively the β configurated glycopeptoid was obtained.
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14. H(1)-H(2) = 9-10 Hz.
15. 2O) and subsequent protection with Fmoc-Cl.