1952
DOI: 10.3891/acta.chem.scand.06-0667
|View full text |Cite
|
Sign up to set email alerts
|

Preparation of Cis- and Trans 2,5-Dimethoxy-2-(acetamidomethyl)-2,5-dihydrofuran, of Cis- and Trans 2,5-Dimethoxy-2-(acetamidomethyl)-tetrahydrofuran and of 1-Phenyl-2-(acetamidomethyl)-pyrrole.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
29
0

Year Published

1990
1990
2017
2017

Publication Types

Select...
5
5

Relationship

0
10

Authors

Journals

citations
Cited by 143 publications
(29 citation statements)
references
References 0 publications
0
29
0
Order By: Relevance
“…Pyrrylarylsulfones were synthesized by arylsulfonation of pyrroles in the presence of potassium tert-butoxide and 18-crown-6 in tetrahydrofuran or via Clauson-Kaas reaction by heating with 2,5-dimethoxytetrahydrofuran in boiling glacial acetic acid [38]. Alkyl 1-(2-nitrophenylsulfonyl)-1H-pyrrole-2-carboxylate were reduced to amino with iron powder in glacial acetic acid (SupplementaRy FiguRe 2).…”
Section: Diarylsulfonesmentioning
confidence: 99%
“…Pyrrylarylsulfones were synthesized by arylsulfonation of pyrroles in the presence of potassium tert-butoxide and 18-crown-6 in tetrahydrofuran or via Clauson-Kaas reaction by heating with 2,5-dimethoxytetrahydrofuran in boiling glacial acetic acid [38]. Alkyl 1-(2-nitrophenylsulfonyl)-1H-pyrrole-2-carboxylate were reduced to amino with iron powder in glacial acetic acid (SupplementaRy FiguRe 2).…”
Section: Diarylsulfonesmentioning
confidence: 99%
“…The resulting precipitates were crystallized with Et2O to give 10 (44.6 g, 93%) as a white powder: 1 H NMR (200 MHz, CDCl3) δ 1.43-1.91 (4H, m), 2.22-2.47 (2H, m), 2.42 (3H, s), 3.41-3.93 (2H, m), 7.05-7.35 (5H, m), 7.52-7.67 (2H, m). 7-Chloro-1,2,3,4-tetrahydro-1H-1-benzazepine (11). To a solution of tosylate 10 (30 g, mmol) in MeOH (300 mL) was slowly added Mg (7.2 g, mmol) to maintain a gentle reflux and H2 evolution.…”
Section: Methodsmentioning
confidence: 99%
“…The synthetic route to obtain MRPy was divided into two steps: i) the preparation of the 1-(3-iodopropyl)pyrrole according to the procedure described by Clauson-Kaas and Tyle [25][26][27], and ii) the esterification step by the nucleophilic substitution reaction of 1-(3-iodopropyl)pyrrole and MR, in the presence of triethylamine/ CH 3 CN (Scheme 1). This method has the advantages of simplicity, mild conditions and good yields from readily available starting materials.…”
Section: Synthesis Of Mrpymentioning
confidence: 99%