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Peptide Enolates. C ‐Alkylation of Glycine Residues in linear tri‐, tetra‐, and pentapeptides via dilithium azadienediolates
Author(s) -
Bossler Hans G.,
Seebach Dieter
Publication year - 1994
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19940770424
Subject(s) - chemistry , sarcosine , tripeptide , alkylation , stereochemistry , tetrapeptide , moiety , peptide , dipeptide , amino acid , residue (chemistry) , dilithium , glycine , electrophile , medicinal chemistry , organic chemistry , deprotonation , catalysis , ion , biochemistry
The Boc‐protected tripeptides Boc‐Val‐Gly‐Leu‐OH ( 1 ), Boc‐Leu‐Sar‐Leu‐OH ( 2 ), Boc‐Leu‐Gly‐MeLeu‐OH ( 3 ), and Boc‐Val‐BzlGly‐Leu‐OMe ( 64 ), tetrapeptide Boc‐Leu‐Gly‐Pro‐Leu‐OH ( 9 ), and pentapeptides Boc‐Val‐Leu‐Gly‐Abu‐Ile‐OH ( 4 ), Boc‐Val‐Leu‐Sar‐MeAbu‐Ile‐OH ( 5 ), Boc‐Val‐Leu‐Gly‐MeAbu‐Ile‐OH ( 6 ), Boc‐Val‐Leu‐BzlGly‐BzlAbu‐Ile‐OH ( 7 ), and Boc‐Val‐Leu‐Gly‐BzlAbu‐Ile‐OH ( 8 ) are prepared by conventional methods ( Schemes 4–7 ) or by direct benzylation of the corresponding precursors ( Scheme 8 ). Polylithiations in THF give up to Li 6 derivatives containing glycine, sarcosine or N ‐benzylglycine Li enolate moieties ( A–H ). The polylithiated systems with a dilithium azadienediolate unit ( C, F–H ) are best generated by treatment with t ‐BuLi. The yields of alkylation of the glycine or sarcosine residues are up to 90%, with diastereoselectivities from nil to 9:1. Normally, the newly formed stereogenic center has ( R )‐configuration ( i.e. a D ‐amino‐acid residue is incorporated in the peptide chain). Electrophiles which can be employed with the highly reactive azadienediolate moiety are: MeI, EtI, i‐PrI, allyl and benzyl bromide, ethyl bromoacetate, CO 2 , and Me 2 S 2 ( Schemes 11–13 ). No epimerizations of the starting materials (racemization of the amino‐acid residues) are observed under the strongly basic conditions. Selected conformations of the peptide precursors, generated by shock‐freezing or by very slow cooling from room temperature to −75° before lithiation, give rise to different stereoselectivities ( Scheme 11 ). The latter and the yields can also be influenced by tempering the lithiated species before ( Scheme 9 ) or after addition of the electrophiles ( Scheme 12 ). Besides the desired products, starting peptides are recovered in the chromatographic purification and isolation procedures (material balance 80–95%). The results described are yet another demonstration that peptides may be backbone‐modified through Li enolates, and that whole series of analogous peptide derivatives with various side chains may thus be produced from a given precursor.