(Q58441273)

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Catalytic enantioselective addition of hydrogen cyanide to benzaldehyde and p-methoxybenzaldehyde using cyclo-His-(α-Me)Phe as catalyst

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Catalytic enantioselective addition of hydrogen cyanide to benzaldehyde and p-methoxybenzaldehyde using cyclo-His-(α-Me)Phe as catalyst (English)

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1 reference

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Ron Hulst

1

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Quirinus B. Broxterman

series ordinal

2

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Johan Kamphuis

series ordinal

3

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Fernando Formaggio

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4

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Marco Crisma

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5

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Claudio Toniolo

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6

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Richard M. Kellogg

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7

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publication date

June 1997

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published in

Tetrahedron: Asymmetry

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volume

8

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issue

12

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page(s)

1987-1999

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cites work

“Synthetic Enzymes”. Highly Stereoselective Epoxidation of Chalcone in a Triphasic Toluene-Water-Poly[(S)-alanine] System

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Synthetic enzymes. Part 2. Catalytic asymmetric epoxidation by means of polyamino-acids in a triphase system

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Terminal epoxidation of farnesate attached to helical peptides

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Stereoselective Organic Reactions: Catalysts for Carbonyl Addition Processes

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Linear oligopeptides. 277. Structural versatility of peptides from C.alpha.,.alpha.-disubstituted glycines. Synthesis, characterization, and solution and crystal-state conformational analysis of homopeptides from C.alpha.-methyl-C.alpha.-isopropylgly

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Structural versatility of peptides from Cα, α-disubstituted glycines: Crystal-state conformational analysis of homopeptides from Cα-methyl, Cα-benzylglycine [(αMe)Phe]n

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Helical screw sense of homo-oligopeptides of Cα-methylated α-amino acids as determined with vibrational circular dichroism

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α-Phenylethylamine based chiral phospholidines; new agents for the determination of the enantiomeric excess of chiral alcohols, amines and thiols by means of 31P NMR

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Identifiers

DOI

10.1016/S0957-4166(97)00178-X

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(Q58441273)

Catalytic enantioselective addition of hydrogen cyanide to benzaldehyde and p-methoxybenzaldehyde using cyclo-His-(α-Me)Phe as catalyst

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