On the allyl protection of the imidazole ring of histidine

Tetrahedron

Volumn 53, Issue 37, 1997, Pages 12525-12538

  Malanda Kimbonguila, A ^a   Boucida, S ^a   Guibe F ^a   Loffet, A ^b,c  

^a UNIVERSITÉ PARIS SACLAY   (France)

^b Propeptide   (France)

^c Senn Chemicals International   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HISTIDINE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; IN VITRO STUDY; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PEPTIDE SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0013521481     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00772-2     Document Type: Article

References (31)

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2. Among many possible references, see for instance: allylic linkers: (a) Llyod-Williams, P.; Merzouk, A.; Guibé, F.; Albericio, F.; Giralt, E. Tetrahedron Lett. 1994, 35, 4437-4440 and refs therein;
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25. 3 to bring about their hydrolysis. As a matter of fact, we were, later on (see scheme 5), able to carry out the catalytic hydrosilylosis of the N (π)-phenacyl-N(τ)-allyl imidazolium bromide 8a and of the N(π)-benzyloxymethyl-N(τ)-allyl-imidazolium chloride 8b without these additives which therefore do not appear to be necessary.
26. Unpublished results from our laboratory.
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