- Unexpectedly rigid short peptide foldamers in which NH-π and CH-π interactions are preserved in solution
-
NH-π and CH-π interactions, due to their weak character, are not easily identified in solution. We report a group of isolable short peptides with stable folds, in which NH-π and CH-π main chain-side chain interactions can be detected in solution by means
- Nara, Masayuki,Ohwada, Tomohiko,Otani, Yuko,Zhai, Luhan
-
supporting information
p. 8344 - 8347
(2021/08/25)
-
- Peptide-based short single β-strand mimics without hydrogen bonding or aggregation
-
Generation of short peptides with a single β-strand structure in solution is difficult. Herein, we design a new class of single β-strand peptidic mimics that are stable without self-aggregation in protic and non-protic solvents. Introduction of one presen
- Zhai, Luhan,Otani, Yuko,Hori, Yukiko,Tomita, Taisuke,Ohwada, Tomohiko
-
supporting information
p. 1573 - 1576
(2020/02/13)
-
- Synthesizing method using serine to prepare Ramipril key intermediate
-
The invention relates to a synthesizing method using serine to prepare a Ramipril key intermediate. The Ramipril key intermediate is 2-azabicyclo[3.3.0] octane-3-carboxylic acid hydrochloride or benzyl ester hydrochloride. The synthesizing method includes: using the serine as the initial raw material, and sequentially performing esterification, acyl chloride acylation, deacidification, Michael addition, hydrolysis and hydrogenation reduction to obtain the Ramipril key intermediate. The synthesizing method has the advantages that the key intermediate is synthesized by a five-step method, and the synthesizing method is cheap in raw material, environmentally friendly, simple in preparation process, simple to operate, mild in reaction condition, short in reaction cycle, convenient in post-treatment, low in equipment requirement, capable of avoiding heavy metal pollution and the use of expensive catalysts, few in three wastes, high in product yield and purity and suitable for industrial production.
- -
-
Paragraph 0065; 0066
(2016/10/10)
-
- Development of an asymmetric hydrogenation route to (S)- N -Boc-2,6-dimethyltyrosine
-
An improved, simpler and potentially more economical route to (S)-N-Boc-2,6-dimethyltyrosine 1, based on a previously published route, is presented. Key modifications were to prepare the dehydroaminoacid hydrogenation substrate 6 in a one-pot process directly from serine methyl ester and 4-iodo-3,5-dimethylphenyl acetate 4 and to identify a significantly more active asymmetric hydrogenation catalyst that allowed a 5-fold reduction in catalyst loading.
- Praquin, Celine F. B.,De Koning, Pieter D.,Peach, Philip J.,Howard, Roger M.,Spencer, Sarah L.
-
experimental part
p. 1124 - 1129
(2012/01/06)
-
- Acetylation under ultrasonic conditions: Convenient preparation of N-acetylamino acids
-
An efficient and simple method of preparation of acetylamino acids from amino acids under ultrasonic conditions is described. The reactions proceed without racemization and the yields are almost quantitative.
- Veera Reddy,Ravindranath
-
p. 257 - 264
(2007/10/02)
-