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Synthesis of a phosphinate analogue of the anti-tumour phosphate di-ester perifosine via sequential radical processes
Тип публикации: Journal Article
Дата публикации: 2013-01-01
scimago Q2
wos Q2
БС1
SJR: 0.6
CiteScore: 5.2
Impact factor: 2.7
ISSN: 14770520, 14770539
PubMed ID:
23073600
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
An efficient synthesis of a phosphinate analogue of the anti-tumour phosphate di-ester perifosine is described (6 steps and 50% overall yield). The two phosphorus-carbon bonds in the perifosine analogue were prepared by sequential double radical hydrophosphinylation processes. This is the first example of a phosphinate analogue of perifosine, designed to be resistant to hydrolysis by phospholipid-metabolizing enzymes.
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ГОСТ
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Markoulides M. S., Regan A. C. Synthesis of a phosphinate analogue of the anti-tumour phosphate di-ester perifosine via sequential radical processes // Organic and Biomolecular Chemistry. 2013. Vol. 11. No. 1. pp. 119-129.
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Markoulides M. S., Regan A. C. Synthesis of a phosphinate analogue of the anti-tumour phosphate di-ester perifosine via sequential radical processes // Organic and Biomolecular Chemistry. 2013. Vol. 11. No. 1. pp. 119-129.
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TY - JOUR
DO - 10.1039/C2OB26395E
UR - https://doi.org/10.1039/C2OB26395E
TI - Synthesis of a phosphinate analogue of the anti-tumour phosphate di-ester perifosine via sequential radical processes
T2 - Organic and Biomolecular Chemistry
AU - Markoulides, Marios S
AU - Regan, Andrew C.
PY - 2013
DA - 2013/01/01
PB - Royal Society of Chemistry (RSC)
SP - 119-129
IS - 1
VL - 11
PMID - 23073600
SN - 1477-0520
SN - 1477-0539
ER -
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BibTex (до 50 авторов)
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@article{2013_Markoulides,
author = {Marios S Markoulides and Andrew C. Regan},
title = {Synthesis of a phosphinate analogue of the anti-tumour phosphate di-ester perifosine via sequential radical processes},
journal = {Organic and Biomolecular Chemistry},
year = {2013},
volume = {11},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/C2OB26395E},
number = {1},
pages = {119--129},
doi = {10.1039/C2OB26395E}
}
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MLA
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Markoulides, Marios S., and Andrew C. Regan. “Synthesis of a phosphinate analogue of the anti-tumour phosphate di-ester perifosine via sequential radical processes.” Organic and Biomolecular Chemistry, vol. 11, no. 1, Jan. 2013, pp. 119-129. https://doi.org/10.1039/C2OB26395E.