Synthesis of enantiopure 7-[3-azidopyl]indolizidin-2-one amino acid. A constrained mimic of the peptide backbone geometry and heteroatomic side-chain functionality of the ala-lys dipeptide.
about
Greener synthesis of indolizine analogues using water as a base and solvent: study for larvicidal activity against Anopheles arabiensis.Intramolecular hydroamination of dithioketene acetals: an easy route to cyclic amino acid derivatives.Intramolecular anodic olefin coupling reactions and the synthesis of cyclic amines.Intramolecular anodic olefin coupling reactions: use of the reaction rate to control substrate/product selectivity.Analysis of N-amino-imidazolin-2-one peptide turn mimic 4-position substituent effects on conformation by X-ray crystallography.
P2860
Synthesis of enantiopure 7-[3-azidopyl]indolizidin-2-one amino acid. A constrained mimic of the peptide backbone geometry and heteroatomic side-chain functionality of the ala-lys dipeptide.
description
2001 nî lūn-bûn
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2001年の論文
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年學術文章
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name
Synthesis of enantiopure 7-[3- ...... lity of the ala-lys dipeptide.
@en
Synthesis of enantiopure 7-[3- ...... lity of the ala-lys dipeptide.
@nl
type
label
Synthesis of enantiopure 7-[3- ...... lity of the ala-lys dipeptide.
@en
Synthesis of enantiopure 7-[3- ...... lity of the ala-lys dipeptide.
@nl
prefLabel
Synthesis of enantiopure 7-[3- ...... lity of the ala-lys dipeptide.
@en
Synthesis of enantiopure 7-[3- ...... lity of the ala-lys dipeptide.
@nl
P356
P1476
Synthesis of enantiopure 7-[3- ...... ality of the ala-lys dipeptide
@en
P2093
P304
P356
10.1021/JO001252L
P407
P577
2001-02-01T00:00:00Z