Synthesis of 4-aminomethyl-tetrahydrofuran-2-carboxylates with 2,4-cis and 2,4-trans relationships
Templated tetrahydrofuran-based γ-azido esters were prepared with the C-2 and C-4 functionalities in cis and trans relative configurations. This was achieved by ring contraction of the suitably protected 2-O-triflates of pentono-1,5-lactones (d-ribose and l-arabinose) with subsequent introduction of...
Prif Awduron: | Edwards, A, Sanjayan, G, Hachisu, S, Soengas, R, Stewart, A, Tranter, G, Fleet, G |
---|---|
Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
2006
|
Eitemau Tebyg
-
A novel series of oligomers from 4-aminomethyl-tetrahydrofuran-2-carboxylates with 2,4-cis and 2,4-trans stereochemistry
gan: Edwards, A, et al.
Cyhoeddwyd: (2006) -
Templated scaffolds of cis- and trans-tetrahydrofuran gamma-amino acids: gamma-azido-beta-hydroxy-tetrahydrofuran-2-carboxylates from pentono-delta-lactones
gan: Sanjayan, G, et al.
Cyhoeddwyd: (2003) -
From sequencamers to foldamers? Tetrameric furanose carbopeptoids from cis- and trans-5-aminomethyl-tetrahydrofuran-2-carboxylates
gan: Long, D, et al.
Cyhoeddwyd: (1999) -
Absence of secondary structure in a carbopeptoid tetramer of a trans-5-aminomethyl-tetrahydrofuran-2-carboxylate
gan: Smith, M, et al.
Cyhoeddwyd: (1999) -
An octameric carbopeptoid; Secondary structure in octameric and tetrameric 5-aminomethyl-tetrahydrofuran-2-carboxylates
gan: Claridge, T, et al.
Cyhoeddwyd: (1999)