1994
DOI: 10.1007/bf00696322
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of ?-formyl-2,5-dialkoxytetrahydrofurans and their reaction with 3-amino-1,2,4-triazole

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
2
0

Year Published

1995
1995
2024
2024

Publication Types

Select...
3
2

Relationship

1
4

Authors

Journals

citations
Cited by 5 publications
(2 citation statements)
references
References 4 publications
0
2
0
Order By: Relevance
“…Claver and co-workers have studied effects that govern the regioselectivity of the hydroformylation of acyclic allyl ethers using Rh catalysts with monodentate phosphines and phosphites. , As expected, α-branching enhances the degree of n -regioselectivity.…”
Section: Substrates and Reactionsmentioning
confidence: 82%
“…Claver and co-workers have studied effects that govern the regioselectivity of the hydroformylation of acyclic allyl ethers using Rh catalysts with monodentate phosphines and phosphites. , As expected, α-branching enhances the degree of n -regioselectivity.…”
Section: Substrates and Reactionsmentioning
confidence: 82%
“…3 In the study of the properties of α substituted 2,5 dimethoxytetrahydrofuran 3 carbalde hydes, 4 we have found that they are hydrolyzed by water to give acetonylmalonaldehyde and its derivatives in vir tually quantitative yields. 5, 6 To investigate this further, we studied acid catalyzed reactions of 2,5 dimethoxy 5 methyltetrahydrofuran 3 carbaldehyde (1) with alcohols.…”
mentioning
confidence: 99%