Home / Publications / Alcoholysis of malonyl peroxides to give peracids

Alcoholysis of malonyl peroxides to give peracids

Margarita Aleksandrovna Lapitskaya 1
Margarita Aleksandrovna Lapitskaya
,  , 
Elena Dmitrievna Daeva 1
Elena Dmitrievna Daeva
,  , 
Kazimir Konstantinovich Pivnitsky 1
Kazimir Konstantinovich Pivnitsky
10.1016/j.mencom.2016.01.006
Published 2015-12-30
Communication , Volume 26, Issue 1, 14-15
7
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Lapitskaya M. A. et al. Alcoholysis of malonyl peroxides to give peracids // Mendeleev Communications. 2015. Vol. 26. No. 1. pp. 14-15.
GOST all authors (up to 50) Copy
Lapitskaya M. A., Vil' V. A., Daeva E. D., Terent'ev A. O., Pivnitsky K. K. Alcoholysis of malonyl peroxides to give peracids // Mendeleev Communications. 2015. Vol. 26. No. 1. pp. 14-15.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2016.01.006
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.006
TI - Alcoholysis of malonyl peroxides to give peracids
T2 - Mendeleev Communications
AU - Lapitskaya, Margarita Aleksandrovna
AU - Vil', Vera Andreevna
AU - Daeva, Elena Dmitrievna
AU - Terent'ev, Alexander Olegovich
AU - Pivnitsky, Kazimir Konstantinovich
PY - 2015
DA - 2015/12/30
PB - Mendeleev Communications
SP - 14-15
IS - 1
VL - 26
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2015_Lapitskaya,
author = {Margarita Aleksandrovna Lapitskaya and Vera Andreevna Vil' and Elena Dmitrievna Daeva and Alexander Olegovich Terent'ev and Kazimir Konstantinovich Pivnitsky},
title = {Alcoholysis of malonyl peroxides to give peracids},
journal = {Mendeleev Communications},
year = {2015},
volume = {26},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.006},
number = {1},
pages = {14--15},
doi = {10.1016/j.mencom.2016.01.006}
}
MLA
Cite this
MLA Copy
Lapitskaya, Margarita Aleksandrovna, et al. “Alcoholysis of malonyl peroxides to give peracids.” Mendeleev Communications, vol. 26, no. 1, Dec. 2015, pp. 14-15. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.006.

Abstract

Potassium acetate catalyzed alcoholysis of spirocycloalkyl malonyl peroxides affords 1-alkoxycarbonylcycloalkane-1-percarboxylic acids which are suitable for epoxidation of olefins.

References

1.
Alkene Syn Dihydroxylation with Malonoyl Peroxides
Griffith J.C., Jones K.M., Picon S., Rawling M.J., Kariuki B.M., Campbell M., Tomkinson N.C.
Journal of the American Chemical Society, 2010
2.
Metal or No Metal: That Is the Question!
Schwarz M., Reiser O.
Angewandte Chemie - International Edition, 2011
3.
Alkene Dihydroxylation with Malonoyl Peroxides: Catalysis Using Fluorinated Alcohols
Picon S., Rawling M., Campbell M., Tomkinson N.C.
Organic Letters, 2012
4.
Metal-Free Dihydroxylation of Alkenes using Cyclobutane Malonoyl Peroxide
Jones K.M., Tomkinson N.C.
Journal of Organic Chemistry, 2012
5.
Metal-free syn-dioxygenation of alkenes
Rawling M.J., Tomkinson N.C.
Organic and Biomolecular Chemistry, 2013
6.
Mechanistic insights into the malonoyl peroxide syn-dihydroxylation of alkenes
Rawling M.J., Rowley J.H., Campbell M., Kennedy A.R., Parkinson J.A., Tomkinson N.C.
Chemical Science, 2014
7.
Terent’ev A.O., Vil’ V.A., Mulina O.M., Pivnitsky K.K., Nikishin G.I.
Mendeleev Communications, 2014
9.
Photochemical transformations. XLIV. Cyclic peroxides. Synthesis and chemistry of .alpha.-lactones
Chapman O.L., Wojtkowski P.W., Adam W., Rodriguez O., Rucktaeschel R.
Journal of the American Chemical Society, 1972
10.
Bis(trifluoromethyl)acetolactone, a Stable a-Lactone'
Adam W., Liu J., Rodriguez O.
Journal of Organic Chemistry, 1973
11.
Triphenylphosphine deoxygenation of malonyl peroxides, a novel route to malonyl anhydrides
Adam W., Diehl J.W.
Journal of the Chemical Society Chemical Communications, 1972
13.
Cyclic peroxides. XVII. Solvolysis of dibutylmalonoyl peroxide
Adam W., Rucktaeschel R.
Journal of Organic Chemistry, 1972
15.
K. M. Jones, PhD Thesis, Cardiff University, 2010, p. 129.
16.
K. M. Jones, PhD Thesis, Cardiff University, 2010, p. 51.
19.
New oxidizing agents from the dehydration of hydrogen peroxide
Rebek J., McCready R., Wolf S., Mossman A.
Journal of Organic Chemistry, 1979
20.
2,3-Epoxy-10-aza-10,11-dihydrosqualene, a high-energy intermediate analogue inhibitor of 2,3-oxidosqualene cyclase.
Ceruti M., Balliano G., Viola F., Grosa G., Rocco F., Cattel L.
Journal of Medicinal Chemistry, 1992