New synthesis of β-keto phosphonates
✍ Scribed by Seongkuk Hong; Kyeongho Chang; Bonchul Ku; Dong Young Oh
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 128 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A new synthetic route to &keto phosphonates from diethyl l-(trimethylsilyl)vinylphosphonate 1 is described. This involves nucleophilic addition of the oryanolithium reagents toward 1 followed by quenchiny with acid chlorides and alkyl isocyanates.
📜 SIMILAR VOLUMES
Reduction of I~-phthalimido-et-keto phosphonates, obtained through an Arbuzov reaction between the appropriate acid chloride and triethyl phosphite, with boranes and oxazaborolidine as catalyst, afforded I~-phthalimido-0t-hydroxy phosphonates in good yields and high diastereoselectivity. Deprotectio
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v