2020
DOI: 10.1016/j.molstruc.2020.127850
|View full text |Cite
|
Sign up to set email alerts
|

Asymmetric synthesis, biological activity and molecular docking studies of some unsaturated α-amino acids, derivatives of glycine, allylglycine and propargylglycine

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
3
0

Year Published

2020
2020
2022
2022

Publication Types

Select...
6

Relationship

1
5

Authors

Journals

citations
Cited by 12 publications
(3 citation statements)
references
References 19 publications
0
3
0
Order By: Relevance
“…In this regard, we would like to stress the growing need in availability and affordability of various tactual types of AAs. Indeed, the interest in the development of synthetic approaches for the preparation of tailor‐made AAs in enantiomerically pure form is currently at an all‐time high 82–135 . Some impressive developments have been made in the area of dynamic kinetic resolution of unprotected AAs, 136–139 a methodology which is best suited for large‐scale production and can rival biocatalytic approaches in affordability and low‐cost structure.…”
Section: Discussionmentioning
confidence: 99%
“…In this regard, we would like to stress the growing need in availability and affordability of various tactual types of AAs. Indeed, the interest in the development of synthetic approaches for the preparation of tailor‐made AAs in enantiomerically pure form is currently at an all‐time high 82–135 . Some impressive developments have been made in the area of dynamic kinetic resolution of unprotected AAs, 136–139 a methodology which is best suited for large‐scale production and can rival biocatalytic approaches in affordability and low‐cost structure.…”
Section: Discussionmentioning
confidence: 99%
“…Even far greater role AAs play in bio‐pharmaceuticals such as peptides, peptidomimetics and proteins [3] . Accordingly, interest in the development of synthetic approaches for the preparation of tailor‐made AAs and their derivatives is currently at an all‐time high [4–21] …”
Section: Introductionmentioning
confidence: 99%
“…Materials and Methods. Non-protein amino acids and peptides used in this study were synthesized at the Scientific and Production Center "Armbiotechnology" NAS RA and Institute of Pharmacy of Yerevan State University [4][5][6][7]. Collagenase G from Clostridium (Hathewaya) histolyticum (EC 3.4.24.3) and miscellaneous reagents were purchased from "Sigma-Aldrich" (now "Merck").…”
mentioning
confidence: 99%