The Enantioselective Synthesis of Conformationally Constrained Cyclic β- Amino Acids
Тип публикации: Journal Article
Дата публикации: 2005-01-01
scimago Q3
wos Q2
БС2
SJR: 0.353
CiteScore: 4.6
Impact factor: 2.3
ISSN: 1570193X, 18756298
Organic Chemistry
Краткое описание
Enantiomerically pure and conformationally constrained cyclic β-amino acids have been the subject of a vast amount of research across the chemical, biological, and medicinal disciplines. These valuable molecules are synthetic precursors for a wide variety of useful compounds that include natural products and modified peptides. Many methods have been developed to prepare chiral cyclic β-amino acids in high optical purity. This mini-review will discuss some of the most recent and successful approaches.
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Miller J. The Enantioselective Synthesis of Conformationally Constrained Cyclic β- Amino Acids // Mini-Reviews in Organic Chemistry. 2005. Vol. 2. No. 1. pp. 39-45.
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Miller J. The Enantioselective Synthesis of Conformationally Constrained Cyclic β- Amino Acids // Mini-Reviews in Organic Chemistry. 2005. Vol. 2. No. 1. pp. 39-45.
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TY - JOUR
DO - 10.2174/1570193052774117
UR - https://doi.org/10.2174/1570193052774117
TI - The Enantioselective Synthesis of Conformationally Constrained Cyclic β- Amino Acids
T2 - Mini-Reviews in Organic Chemistry
AU - Miller, Jason
PY - 2005
DA - 2005/01/01
PB - Bentham Science Publishers Ltd.
SP - 39-45
IS - 1
VL - 2
SN - 1570-193X
SN - 1875-6298
ER -
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@article{2005_Miller,
author = {Jason Miller},
title = {The Enantioselective Synthesis of Conformationally Constrained Cyclic β- Amino Acids},
journal = {Mini-Reviews in Organic Chemistry},
year = {2005},
volume = {2},
publisher = {Bentham Science Publishers Ltd.},
month = {jan},
url = {https://doi.org/10.2174/1570193052774117},
number = {1},
pages = {39--45},
doi = {10.2174/1570193052774117}
}
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MLA
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Miller, Jason. “The Enantioselective Synthesis of Conformationally Constrained Cyclic β- Amino Acids.” Mini-Reviews in Organic Chemistry, vol. 2, no. 1, Jan. 2005, pp. 39-45. https://doi.org/10.2174/1570193052774117.