Synthesis of 4-hydroxymethyl-2,4-methanoproline
-
Add time:08/30/2019 Source:sciencedirect.com
The synthesis of 4-hydroxymethyl-2,4-methanoproline, a novel conformationally restricted amino acid, was performed in four steps. This close analogue of naturally occurring amino acids (i.e., proline, hydroxyproline, serine and threonine) was prepared in good overall yield through two intramolecular recyclization reactions of cyclobutane derivatives.
We also recommend Trading Suppliers and Manufacturers of 1,2-bis-(Hydroxymethyl)-o-carborane (cas 19610-37-8). Pls Click Website Link as below: cas 19610-37-8 suppliers
Prev:Preparation of 1,2-bis(3,4-dicyanophenoxymethyl)benzene and the binuclear zinc phthalocyanine derived from it
Next:Mini-reviewThe development of bis(hydroxymethyl)pyrrole analogs as bifunctional DNA cross-linking agents and their chemotherapeutic potential) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Mini-reviewThe development of bis(hydroxymethyl)pyrrole analogs as bifunctional DNA cross-linking agents and their chemotherapeutic potential08/31/2019
- Preparation of 1,2-bis(3,4-dicyanophenoxymethyl)benzene and the binuclear zinc phthalocyanine derived from it08/29/2019
- Synthesis of 5-hydroxymethyl furfural from cellulose via a two-step process in polar aprotic solvent08/28/2019
- Original articleChiral 6,7-bis(hydroxymethyl)-1H,3H-pyrrolo[1,2-c]thiazoles with anti-breast cancer properties08/27/2019
- “2-Amino glucose” as a substrate for synthesis of magnetically recoverable nanocatalyst NiFe2O4@SiO2@amino glucose for the green synthesis of novel bis (1,2-dihydro-4-hydroxy-2-oxoquinolin-3-yl)methanes08/26/2019
- Practical way for the synthesis of 3,3′-bis-substituted benzo[d][1,2]oxaphosphole 2-oxides by phosphonylation of in situ generated o-quinone methides08/25/2019
- Original articleTargeting triple-negative breast cancer cells with 6,7-bis(hydroxymethyl)-1H,3H-pyrrolo[1,2-c]thiazoles08/24/2019


