silyl phosphite
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Enantioselective dearomatization of isoquinolines by anion-binding catalysis en route to cyclic α-aminophosphonates

Chemical Science ◽

10.1039/c6sc02466a ◽

2016 ◽

Vol 7 (12) ◽

pp. 6940-6945 ◽

Cited By ~ 31

Author(s):

Abhijnan Ray Choudhury ◽

Santanu Mukherjee

Keyword(s):

Anion Binding ◽

Silyl Phosphite

An enantioselective dearomatization of isoquinolines has been developed using chiral anion-binding catalysis. This transformation makes use of silyl phosphite as a nucleophile and generates cyclic α-aminophosphonates.

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Silyl-Phosphite Chemistry

Encyclopedia of Genetics, Genomics, Proteomics and Informatics ◽

10.1007/978-1-4020-6754-9_15639 ◽

2008 ◽

pp. 1818-1818

Keyword(s):

Silyl Phosphite

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Silyl-Phosphite Chemistry

Encyclopedic Dictionary of Genetics, Genomics and Proteomics ◽

10.1002/0471684228.egp11584 ◽

2004 ◽

Keyword(s):

Silyl Phosphite

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Nucleoside H-phosphonates. Part 16.31P NMR studies on the transformation of nucleoside H-phosphonate monoesters into a monofunctional tervalent intermediate, nucleoside acyl silyl phosphite

Journal of the Chemical Society Perkin Transactions 2 ◽

10.1039/p29960000795 ◽

1996 ◽

pp. 795-799 ◽

Cited By ~ 5

Author(s):

Rula Zain ◽

Jacek Stawiński

Keyword(s):

Nmr Studies ◽

Silyl Phosphite

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ChemInform Abstract: PROTECTION OF PHOSPHONATE FUNCTION BY MEANS OF ETHOXYCARBONYL GROUP. A NEW METHOD FOR GENERATION OF REACTIVE SILYL PHOSPHITE INTERMEDIATES

Chemischer Informationsdienst ◽

10.1002/chin.198218336 ◽

1982 ◽

Vol 13 (18) ◽

Author(s):

M. SEKINE ◽

H. MORI ◽

T. HATA

Keyword(s):

New Method ◽

Group A ◽

Silyl Phosphite

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ChemInform Abstract: SILYL PHOSPHITE EQUIVALENTS: 2,2,2-TRICHLOROETHOXYCARBONYLPHOSPHONATES

Chemischer Informationsdienst ◽

10.1002/chin.198204263 ◽

1982 ◽

Vol 13 (4) ◽

Author(s):

M. SEKINE ◽

H. YAMAGATA ◽

T. HATA

Keyword(s):

Silyl Phosphite

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Protection of Phosphonate Function by Means of Ethoxycarbonyl Group. A New Method for Generation of Reactive Silyl Phosphite Intermediates

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.55.239 ◽

1982 ◽

Vol 55 (1) ◽

pp. 239-242 ◽

Cited By ~ 15

Author(s):

Mitsuo Sekine ◽

Hiroyuki Mori ◽

Tsujiaki Hata

Keyword(s):

New Method ◽

Group A ◽

Silyl Phosphite

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Silyl phosphite equivalents: 2,2,2-trichloroethoxycarbonylphosphonates

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39810000970 ◽

1981 ◽

pp. 970 ◽

Cited By ~ 2

Author(s):

Mitsuo Sekine ◽

Hikaru Yamagata ◽

Tsujiaki Hata

Keyword(s):

Silyl Phosphite

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silyl phosphiteRecently Published Documents

TOTAL DOCUMENTS

H-INDEX

Enantioselective dearomatization of isoquinolines by anion-binding catalysis en route to cyclic α-aminophosphonates

Silyl-Phosphite Chemistry

Silyl-Phosphite Chemistry

Nucleoside H-phosphonates. Part 16.31P NMR studies on the transformation of nucleoside H-phosphonate monoesters into a monofunctional tervalent intermediate, nucleoside acyl silyl phosphite

ChemInform Abstract: PROTECTION OF PHOSPHONATE FUNCTION BY MEANS OF ETHOXYCARBONYL GROUP. A NEW METHOD FOR GENERATION OF REACTIVE SILYL PHOSPHITE INTERMEDIATES

ChemInform Abstract: SILYL PHOSPHITE EQUIVALENTS: 2,2,2-TRICHLOROETHOXYCARBONYLPHOSPHONATES

Protection of Phosphonate Function by Means of Ethoxycarbonyl Group. A New Method for Generation of Reactive Silyl Phosphite Intermediates

Silyl phosphite equivalents: 2,2,2-trichloroethoxycarbonylphosphonates

silyl phosphite
Recently Published Documents