Journal article

Synthesis of oligomers of tetrahydrofuran amino acids: furanose carbopeptoids

Abstract:: An acid catalysed ring rearrangement of a triflate derivative of D-mannono-γ-lactone 6 is the key step in the synthesis of the C-glycosyl sugar amino acid derivatives 3 and 4, examples of carbohydrate amino acid building blocks with specific conformational preferences suitable for incorporation into combinatorial amide libraries; homo-oligomerisation via solution phase coupling procedures affords furanose carbopeptoids 1 which adopt novel solution state secondary structures.

Publication status:: Published

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APA Style

Smith, M., Long, D., Marquess, D., Claridge, T., & Fleet, G. (1998). Synthesis of oligomers of tetrahydrofuran amino acids: furanose carbopeptoids. CHEMICAL COMMUNICATIONS, 18, 2039–2040.

MLA Style

Smith, M., et al. “Synthesis of Oligomers of Tetrahydrofuran Amino Acids: Furanose Carbopeptoids.” CHEMICAL COMMUNICATIONS, no. 18, 1998, pp. 2039–40.

Chicago Style

Smith, M, D Long, D Marquess, T Claridge, and G Fleet. 1998. “Synthesis of Oligomers of Tetrahydrofuran Amino Acids: Furanose Carbopeptoids.” CHEMICAL COMMUNICATIONS, no. 18: 2039–40.
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Publisher copy:: 10.1039/a805364b

Authors

+ Smith, M More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

+ Long, D More by this author

Role:: Author

+ Marquess, D More by this author

Role:: Author

+ Claridge, T More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

+ Fleet, G More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

Journal:: CHEMICAL COMMUNICATIONS More from this journal
Issue:: 18
Pages:: 2039-2040
Publication date:: 1998-09-21
DOI:: 10.1039/a805364b
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:36733
UUID:: uuid:d699a726-77db-4180-9ff2-3d7f216d1bc3
Local pid:: pubs:36733
Source identifiers:: 36733
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1998

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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