1993
DOI: 10.1070/rc1993v062n08abeh000045
|View full text |Cite
|
Sign up to set email alerts
|

Methods of synthesis of acrolein and its α-substituted derivatives

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
3
0

Year Published

2000
2000
2021
2021

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 8 publications
(3 citation statements)
references
References 43 publications
0
3
0
Order By: Relevance
“…Meanwhile, many years have passed since the publication of the last review devoted to the chemistry of α-functionally substituted acrolein derivatives. Indeed, this review only covered the synthetic approaches to acrolein and its α-substituted analogs developed before 1993 [ 10 ]. There were other survey publications on this topic, in which, however, 2-functionally substituted 2-alkenals were only described partially.…”
Section: Introductionmentioning
confidence: 99%
“…Meanwhile, many years have passed since the publication of the last review devoted to the chemistry of α-functionally substituted acrolein derivatives. Indeed, this review only covered the synthetic approaches to acrolein and its α-substituted analogs developed before 1993 [ 10 ]. There were other survey publications on this topic, in which, however, 2-functionally substituted 2-alkenals were only described partially.…”
Section: Introductionmentioning
confidence: 99%
“…On the other hand, the multiple functional groups incorporated in these compounds suggest that they should serve as valuable synthetic building blocks in a number of applications. Unfortunately, the anticipated sensitivity of these enynals limits the range of methods potentially applicable for their preparation, and to date the synthetic utility of this class of aldehydes remains unrealized …”
mentioning
confidence: 99%
“…Aliphatic 2-alkoxy-and 2-alkylthioalkenals have been synthesized using a number of different protocols. 2,6 The most common procedure involves the aminomethylation of the corresponding alkoxy-or aryloxyacetaldehydes followed by the decomposition of hydrochloride Mannich base. 7 The attempts to prepare 2-alkylthiopropenals by either Mannich reaction 8 or alkylsulfenylchlorination of acrolein with subsequent dehydrochlorination of the adduct 9 almost always result in the isolation of cyclic dimers, namely 2-formyl-2,5-dialkylthio-2,3-dihydro-4Н-pyranes.…”
Section: Introductionmentioning
confidence: 99%