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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

発表形態:
原著論文
主要業績:
主要業績
単著・共著:
共著
発表年月:
2017年01月
DOI:
10.1016/j.tetasy.2016.11.005
会議属性:
指定なし
査読:
有り
リンク情報:

日本語フィールド

著者:
Saga, Yuta; Saga, Yuta; Mino, Yuka; Kawaguchi, Shin ichi; Han, Daoqing; Ogawa, Akiya; Han, Li Biao
題名:
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
発表情報:
Tetrahedron Asymmetry 巻: 28 号: 1 ページ: 8489
キーワード:
概要:
© 2016 Elsevier Ltd 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.
抄録:

英語フィールド

Author:
Saga, Yuta; Saga, Yuta; Mino, Yuka; Kawaguchi, Shin ichi; Han, Daoqing; Ogawa, Akiya; Han, Li Biao
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
Announcement information:
Tetrahedron Asymmetry Vol: 28 Issue: 1 Page: 8489
An abstract:
© 2016 Elsevier Ltd 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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