![]() This reaction may be used to effect the overall transformation of a ketone to an alkene. The usage of aprotic solvent gives predominantly Z-alkenes, while protic solvent gives a mixture of E- and Z-alkenes. The Bamford–Stevens reaction is a chemical reaction whereby treatment of tosylhydrazones(p-Toluenesulfonyl hydrazones)with strong base gives alkenes.It is named for the British chemist William Randall Bamford and the Scottish chemist Thomas Stevens (1900–2000). Clicking on the donut icon will load a page at with additional details about the score and the social media presence for the given article. The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. These metrics are regularly updated to reflect usage leading up to the last few days. Learn more about these metrics Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. The advantage of the Shapiro over Bamford-Stevens Reaction is, that the resulting dianion does not tend to rearrange, which can. In aprotic conditions (sodium methoxide in. ![]() Bamford Biographical references: Campbell, W.A. (also in the Collective Volume (1990) 7:438 (PDF)) ^ Sarkar. The Bamford–Stevens reaction has not proved useful for the stereoselective generation of alkenes via. ![]()
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