2017
DOI: 10.1007/s10600-017-1984-5
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of 1,2,3-Triazole Derivatives from 2,3-Dienoates of Methyl Maleopimarate

Abstract: Hybrid compounds based on N-maleopimarimides containing a triazole-ring pharmacophore were prepared via 1,3-dipolar cycloaddition of methyl-2-azidoacetate to allenoates.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2018
2018
2020
2020

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 11 publications
(1 citation statement)
references
References 6 publications
0
1
0
Order By: Relevance
“…In conformity with the formulated goal and its solution, methane fullerenes with maleopimarimide fragments, which were not described in the scientific literature, have been chosen as test compounds. The synthesis of chloro‐ 3a–d and bromomethyl ketones 4a–d has been carried out on the basis of the previously obtained N ‐maleopyrimarimide‐substituted carboxylic acids 1a–d . Linear amino acids as starting ones were further converted into the spacer element, with the length of the carbon chain from n = 1 to n = 5.…”
Section: Resultsmentioning
confidence: 99%
“…In conformity with the formulated goal and its solution, methane fullerenes with maleopimarimide fragments, which were not described in the scientific literature, have been chosen as test compounds. The synthesis of chloro‐ 3a–d and bromomethyl ketones 4a–d has been carried out on the basis of the previously obtained N ‐maleopyrimarimide‐substituted carboxylic acids 1a–d . Linear amino acids as starting ones were further converted into the spacer element, with the length of the carbon chain from n = 1 to n = 5.…”
Section: Resultsmentioning
confidence: 99%