1,1-Di-iodoalkenes from aldehydes and triphenylphosphine–carbon tetraiodide
作者:Francisco Gaviña、Santiago V. Luis、Patrick Ferrer、Ana M. Costero、J. Alberto Marco
DOI:10.1039/c39850000296
日期:——
The Wittig-like transformation of aliphatic and aromatic aldehydes into 1,1-di-iodoalkenes can be achieved with triphenylphosphine–carbontetraiodide.
脂族和芳族醛类的Wittig样转化为1,1-二碘代烯烃可通过三苯基膦-四碘化碳实现。
GAVINA, F.;LUIS, S. V.;FERRER, P.;COSTERO, A. M.;MARCO, J. A., J. CHEM. SOC. CHEM. CMMUN., 1985, N 5, 296-297
作者:GAVINA, F.、LUIS, S. V.、FERRER, P.、COSTERO, A. M.、MARCO, J. A.
DOI:——
日期:——
GAVINA F.; LUIS S. V.; FERRER P.; COSTERO A. M.; MARCO J. A., J. CHEM. RES. SYNOP.,(1986) N 9, 330-331
作者:GAVINA F.、 LUIS S. V.、 FERRER P.、 COSTERO A. M.、 MARCO J. A.
DOI:——
日期:——
Highly Efficient Two-Step Synthesis of C-sp<sup>3</sup>-Centered Geminal Diiodides
作者:Jean-Manuel Cloarec、André B. Charette
DOI:10.1021/ol047997l
日期:2004.12.1
[reaction: see text] Trisubstituted gem-diiodoalkenes of functionalized chains are efficiently reduced to the corresponding terminal geminaldiiodides in high yields upon treatment with the diazene precursor, diethyl 4-(hydrazinosulfonyl)-benzyl phosphonate.