CORE
🇺🇦
make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Reaction of pyridoxal and its azomethines with hydrophosphoryl compounds
Authors
Burilov A.
Dobrynin A.
+4 more
Kibardina L.
Pudovik E.
Pudovik M.
Trifonov A.
Publication date
1 January 2016
Publisher
Abstract
© 2016 Taylor & Francis Group, LLC.The products of carbonyl phosphonylation of pyridoxal with alkylphosphinic acid ethyl esters, phosphorous acid dialkyl esters have been obtained for the first time. In some cases, the products of addition are hydrolytically unstable and stabilize by forming internal betaine structures. The reaction of pyridoxal with phosphorous acid in alcohol solutions gives alkoxyfuropyridines possessing the iminium nitrogen atom
Similar works
Full text
Open in the Core reader
Download PDF
Available Versions
Kazan Federal University Digital Repository
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:dspace.kpfu.ru:net/114417
Last time updated on 07/05/2019
Kazan Federal University Digital Repository
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:dspace.kpfu.ru:net/143302
Last time updated on 07/05/2019