Chiral o-methoxyaryldiazaphosphonamides -: A new class of efficient lewis bases in the catalytic asymmetric ring opening of cyclooctene oxide with silicon tetrachloride (vol 218, pg 4536, 2002)

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作者：

Buono, G

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EUROPEAN JOURNAL OF ORGANIC CHEMISTRY | 2002年 / 2002卷 / 07期

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O62 [有机化学];

学科分类号：

070303 ; 081704 ;

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页码：1337 / 1337

页数：1

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[1] Chiral o-methoxyaryldiazaphosphonamides -: A new class of efficient Lewis bases in the catalytic asymmetric ring opening of cyclooctene oxide with silicon tetrachloride
Reymond, S
Legrand, O
Brunel, JM
Buono, G
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2001, 2001 (15) : 2819 - 2823
[2] Beneficial effect of ortho-methoxy groups in the asymmetric ring opening of meso epoxides with silicon tetrachloride catalyzed by chiral ortho-methoxyphenyl-diazaphosphonamide Lewis bases
Brunel, JM
Legrand, O
Reymond, S
Buono, G
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2000, 39 (14) : 2554 - +
[3] Beneficial effect of ortho-methoxy groups in the asymmetric ring opening of meso epoxides with silicon tetrachloride catalyzed by chiral ortho-methoxyphenyl-diazaphosphonamide Lewis bases
Brunel, Jean Michel
Legrand, Olivier
Reymond, Sebastien
Buono, Gerard
Angewandte Chemie (International Edition in English), 2000, 39 (14): : 2554 - 2557
[4] A recyclable chiral Ru catalyst for enantioselective olefin metathesis. Efficient catalytic asymmetric ring-opening/cross metathesis in air (vol 124, pg 4954, 2002)
Van Veldhuizen, JJ
Garber, SB
Kingsbury, JS
Hoveyda, AH
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (41) : 12666 - 12666
[5] Beneficial effect of ortho-methoxy groups in the asymmetric ring opening of meso epoxides with silicon tetrachloride catalyzed by chiral ortho-methoxyphenyldiazaphosphonamide Lewis bases -: Response to the communication by G.!Buono et al.
Denmark, SE
Wynn, T
Jellerichs, BG
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2001, 40 (12) : 2255 - +