REACTION OF THE LITHIUM DERIVATIVE OF DIETHYL 2-(OR 3-)METHYLPHENYLMETHANEPHOSPHONATE WITH KETONES. AN EXAMPLE OF HIGH SYN-STEREOSELECTIVITY
Author:
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/10426509308038181
Reference15 articles.
1. STEREOSELECTIVITY OF THE WITTIG-HORNER REACTION WITH BENZYLPHOSPHONATE CARBANIONS AND ALDEHYDES
2. REACTION OF LITHIUM DERIVATIVE OF DIETHYL PHENYLMETHANE-PHOSPHONATE WITH KETONES
3. OLEFIN SYNTHESIS USING LITHIUM DERIVATIVES OFN,N,N',N'-TETRAMETHYLDIAMIDES OF ARYLMETHANEPHOSPHONIC ACIDS
4. OLEFIN SYNTHESIS VIA THE LITHIUM DERIVATIVES OF THE N,N,N,N′-TETRAMETHYLDIAMIDES OF ARYLMETHANEPHOSPHONIC ACIDS. 2. SYNTHESIS OF SOME (Z)-ORTHO-AND PARA-SUBSTITUTED STILBENES
5. OLEFIN SYNTHESIS VIA THE LITHIUM DERIVATIVE OF THEN,N,N′,N′-TETRAMETHYLDIAMIDES OF ARYLMETHANEPHOSPHONIC ACIDS. 3 SYNTHESIS OF SOME β-DISUBSTITUTED STYRENES
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2. ChemInform Abstract: Reaction of the Lithium Derivative of Diethyl 2-(or 3-) Methylphenylmethanephosphonate with Ketones. An Example of High Syn- Stereoselectivity.;ChemInform;2010-08-19
3. The Synthesis of Functionalized Phosphinic and Phosphonic Acids and their Derivatives. Part A: Halo, Hydroxy, Epoxy, Mercapto, Carboxy and Oxo Functionalized Acids;PATAI'S Chemistry of Functional Groups;2009-12-15
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