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tert-butoxycarbonyl-tyrosyl-leucyl-valyl-chloromethane
Known as:
t-butoxycarbonyl-Tyr-Leu-Val-CH2Cl
, tB-YLV cpd
National Institutes of Health
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1 relation
Broader (1)
Oligopeptides
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2009
2009
Hono-oligohistidines. II: Preferred conformations in solution of a series of N(α-t-butoxycarbonyl, N(π)-benzyloxyméthyl-homo-oligo-L-histidine méthyl esters, from the dipeptide to the heptapeptide
G. Bonora
,
C. Toniolo
,
J. Jones
,
K. Rajasekharan
2009
Corpus ID: 84166795
1988
1988
A fluoride ion deprotection strategy in peptide synthesis. Combination with selective deprotection using the dilute methanesulfonic acid of alpha-amino protecting groups.
Yoshiaki Kiso
,
T. Kimura
,
Y. Fujiwara
,
Masanori Shimokura
,
A. Nishitani
Chemical and pharmaceutical bulletin
1988
Corpus ID: 43064101
We have developed a novel orthogonal protection methodology in peptide synthesis which involves two classes of acid-labile…
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