The PMe3-catalyzed addition of enantiomerically pure (−)-MenthylO(Ph)P(O)H to electron-deficient alkenes: an efficient way for the preparation of P-stereogenic compounds
Тип публикации: Journal Article
Дата публикации: 2017-01-01
Catalysis
Organic Chemistry
Inorganic Chemistry
Physical and Theoretical Chemistry
Краткое описание
A variety of P -stereogenic organophosphorus compounds can be readily prepared by stereoretentive addition. The PMe 3 -catalyzed addition of optically active (−)MenthylO(Ph)P(O)H compounds to electron deficient alkenes occur stereospecifically, to produce the corresponding P -stereogenic adducts in high yields. By simply removing the volatiles under vacuum, spectroscopically pure products can be obtained. The present method provides a salt-free clean process for the preparation of P -chiral organophosphorus compounds.
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Saga Y. et al. The PMe3-catalyzed addition of enantiomerically pure (−)-MenthylO(Ph)P(O)H to electron-deficient alkenes: an efficient way for the preparation of P-stereogenic compounds // Tetrahedron Asymmetry. 2017. Vol. 28. No. 1. pp. 84-89.
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Saga Y., Mino Y., KAWAGUCHI S., Han D., Ogawa A., Han L. The PMe3-catalyzed addition of enantiomerically pure (−)-MenthylO(Ph)P(O)H to electron-deficient alkenes: an efficient way for the preparation of P-stereogenic compounds // Tetrahedron Asymmetry. 2017. Vol. 28. No. 1. pp. 84-89.
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TY - JOUR
DO - 10.1016/j.tetasy.2016.11.005
UR - https://doi.org/10.1016/j.tetasy.2016.11.005
TI - The PMe3-catalyzed addition of enantiomerically pure (−)-MenthylO(Ph)P(O)H to electron-deficient alkenes: an efficient way for the preparation of P-stereogenic compounds
T2 - Tetrahedron Asymmetry
AU - Saga, Yuta
AU - Mino, Yuka
AU - KAWAGUCHI, SHINICHI
AU - Han, Daoqing
AU - Ogawa, Akiya
AU - Han, Libiao
PY - 2017
DA - 2017/01/01
PB - Elsevier
SP - 84-89
IS - 1
VL - 28
SN - 0957-4166
SN - 1362-511X
ER -
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@article{2017_Saga,
author = {Yuta Saga and Yuka Mino and SHINICHI KAWAGUCHI and Daoqing Han and Akiya Ogawa and Libiao Han},
title = {The PMe3-catalyzed addition of enantiomerically pure (−)-MenthylO(Ph)P(O)H to electron-deficient alkenes: an efficient way for the preparation of P-stereogenic compounds},
journal = {Tetrahedron Asymmetry},
year = {2017},
volume = {28},
publisher = {Elsevier},
month = {jan},
url = {https://doi.org/10.1016/j.tetasy.2016.11.005},
number = {1},
pages = {84--89},
doi = {10.1016/j.tetasy.2016.11.005}
}
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MLA
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Saga, Yuta, et al. “The PMe3-catalyzed addition of enantiomerically pure (−)-MenthylO(Ph)P(O)H to electron-deficient alkenes: an efficient way for the preparation of P-stereogenic compounds.” Tetrahedron Asymmetry, vol. 28, no. 1, Jan. 2017, pp. 84-89. https://doi.org/10.1016/j.tetasy.2016.11.005.