2021
DOI: 10.1016/j.carres.2021.108458
|View full text |Cite
|
Sign up to set email alerts
|

Screening of simple carbohydrates as a renewable organocatalyst for the efficient construction of 1,3-benzoxazine scaffold

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2022
2022
2023
2023

Publication Types

Select...
5

Relationship

1
4

Authors

Journals

citations
Cited by 5 publications
(2 citation statements)
references
References 66 publications
0
2
0
Order By: Relevance
“…With this program, pKa values of nitrogen in the imidazole ring (CH = N), nitrogen in the imine group (CH = N), nitrogen-bound hydrogen in the imidazole ring (N-H), and oxygen-bound hydrogen in the phenol structure (O-H) were calculated. In the calculation, Mode: macro, Acid / base prefix: dynamic, Min basic pKa: -2, Max acidic pKa: 16 and Temperatura (K): 298 were selected [31]. The stacked pKa results are given in Table 7.…”
Section: Marvinsketch Methodsmentioning
confidence: 99%
“…With this program, pKa values of nitrogen in the imidazole ring (CH = N), nitrogen in the imine group (CH = N), nitrogen-bound hydrogen in the imidazole ring (N-H), and oxygen-bound hydrogen in the phenol structure (O-H) were calculated. In the calculation, Mode: macro, Acid / base prefix: dynamic, Min basic pKa: -2, Max acidic pKa: 16 and Temperatura (K): 298 were selected [31]. The stacked pKa results are given in Table 7.…”
Section: Marvinsketch Methodsmentioning
confidence: 99%
“…Moreover, surfactant-catalyzed reactions carried out in aqueous medium or in organic solvents including water phase still maintain their popularity. As a part of our continual work toward the progress of sustainable methods for preparation of valuable compounds with various heterocyclic ring systems [25][26][27][28][29][30][31], we wish to report here a sustainable protocol toward biologically active compounds. In the literature, terpenone and carbohydrate based some natural carbonyl compounds were chosen as starting materials, and chiral Δ 2 -1,3,4-thiadiazoline derivatives with biological activity were synthesized and some mechanistic approaches were discussed [32][33][34][35][36][37][38][39][40].…”
Section: Introductionmentioning
confidence: 99%