Synthesis of 2-azaspiro[3.3]heptane-derived amino acids: ornitine and GABA analogues-Reference-Cited by-同舟云学术

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Synthesis of 2-azaspiro[3.3]heptane-derived amino acids: ornitine and GABA analogues

Published:2010-01-27 Issue:2 Volume:39 Page:515-521
ISSN:0939-4451
Container-title:Amino Acids
language:en
Short-container-title:Amino Acids

Author:

Radchenko Dmytro S.,Grygorenko Oleksandr O.,Komarov Igor V.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Clinical Biochemistry,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s00726-009-0467-9.pdf

Reference20 articles.

1. Allinger NL, Tushaus LA (1965) Conformational Analysis. XLIII. Stereochemical studies in the cyclobutane ring system. J Org Chem 65:1945–1951. doi: 10.1021/jo01017a057

2. Avenoza A, Cativiela C, Busto JH, Fernández-Recio MA, Peregrina JM, Rodrígues F (2001) New synthesis of 7-azabicyclo[2.2.1]heptane-1-carboxylic acid. Tetrahedron 57:545–548. doi: 10.1016/S0040-4020(00)01023-1

3. Cativiela C, Ordóñez M (2009) Recent progress on the stereoselective synthesis of cyclic quaternary α-amino acids. Tetrahedron Asymmetry 20(1):1–63. doi: 10.1016/j.tetasy.2009.01.002

4. Cowell SM, Lee YS, Cain JP, Hruby VJ (2004) Exploring Ramachandran and chi space: conformationally constrained amino acids and peptides in the design of bioactive polypeptide ligands. Curr Med Chem 11(21):2785–2798. doi: 10.2174/0929867043364270

5. de Meijere A, Ernst K, Zuck B, Brandl M, Kozhushkov SI, Tamm M, Yufit DS, Howard JAK, Labahn T (1999) Cyclopropyl building blocks for organic synthesis, 53. Convenient syntheses of novel α- and β-amino acids with spiropentyl groups. Eur J Org Chem 1999(11):3105–3115. doi: 10.1002/(SICI)1099-0690(199911)1999:11<3105::AID-EJOC3105>3.0.CO;2-1

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1. Spiro[2.3]hexane‐ and Spiro[3.3]heptane‐derived α‐Amino Acids: Synthesis and Isoelectric Point Evaluation;ChemistrySelect;2024-08-14

2. 1‐Azaspiro[3.3]heptane as a Bioisostere of Piperidine**;Angewandte Chemie International Edition;2023-11-14

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4. Synthesis of challenging 6-functionalized 1-oxaspiro[3.3]heptanes – New scaffolds for drug discovery;Tetrahedron Letters;2023-06

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