156420-52-9Relevant academic research and scientific papers
Reactions of stannaphosphenes with α-ethylene aldehydes and ketones
Kandri-Rodi,Ranaivonjatovo,Escudié
, p. 2787 - 2791 (2008/10/08)
Stannaphosphene Is2Sn=PAr (1) (Is, 2,4,6-triisopropylphenyl; Ar, 2,4,6-tri-tert-butylphenyl) gives with various α-ethylene aldehydes and ketones exclusive [2 + 4] cycloadditions, leading to the corresponding six-membered ring stannaoxaphosphorinenes 2-7. A comparison with the reactivity of germaphosphenes toward the same carbonyl compounds is described. The inversion barrier of phosphorus has been determined for cycloadducts 2 (acrolein) and 3 (methacrolein) (respectively 12.9 and 13.0 kcal/mol) by dynamic proton NMR. The very low values observed are mainly due to the large steric hindrance of groups on phosphorus. The rotational barrier of the Is group cis to the Ar group has been determined in 2 and 3, as well as the rotational barrier of the Ar group in 2-4 (cycloadduct with crotonaldehyde).
SYNTHESIS AND REACTIVITY OF NEW GERMA- AND STANNAPHOSPHENES
Ranaivonjatovo, H.,Escudie, J.,Couret, C.,Rodi, A. Kandri,Satge, J.
, p. 61 - 64 (2007/10/02)
New stable compounds with a germanium (or a tin)-phosphorus double bond have been prepared respectively by a one step reaction between a lithiophosphide and a difluorogermane, or by dehydrofluorination of the corresponding fluorostannyl-phosphine with tert-butyllithium.Various types of cycloadditions (, and ) have been observed with aldehydes, nitrones and α-ethylenic aldehydes and ketones.
