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The world of beta- and gamma-peptides comprised of homologated proteinogenic amino acids and other components.
- D. Seebach, A. Beck, Daniel J. Bierbaum
- Biology, ChemistryChemistry & biodiversity
- 2004
TLDR
The World of β‐ and γ‐Peptides Comprised of Homologated Proteinogenic Amino Acids and Other Components
- D. Seebach, A. Beck, Daniel J. Bierbaum
- Biology, Chemistry
- 1 August 2004
TLDR
TADDOLs, Their Derivatives, and TADDOL Analogues: Versatile Chiral Auxiliaries.
- D. Seebach, A. Beck, A. Heckel
- ChemistryAngewandte Chemie
- 5 January 2001
TLDR
Solubilization of Peptides in Non‐polar Organic Solvents by the Addition of Inorganic Salts: Facts and Implications
- D. Seebach, A. Thaler, A. Beck
- Chemistry
- 9 August 1989
The solubility of open-chain peptide derivatives (12 examples) in non-polar, ether-type organic solvents may be greatly increased by addition of salts (LiCl, LiBr, LiI, LiBF4, LiClO4, NaI, MgBr2…
Antibacterial Activity of Enrofloxacin and Ciprofloxacin Derivatives of β‐Octaarginine
- N. Purkayastha, S. Capone, H. Moser
- Biology, Materials ScienceChemistry & biodiversity
- 1 February 2015
TLDR
On the Mechanisms of Enantioselective Reactions Using α,α,α′,α′ -Tetraaryl-1,3-dioxolane-4,5-dimethanol(TADDOL)-Derived Titanates: Differences between C2- and C1-symmetrical TADDOLs – facts,…
- D. Seebach, D. Plattner, A. Beck, Y. Wang, D. Hunziker, W. Petter
- Chemistry
- 11 November 1992
The titanates derived from α,α,α′,α′-tetraaryl-1,3-dioxolane-4,5-dimethanols (TADDOLs, prepared from tartrate) act as catalysts for enantioselective additions of dialkylzinc compounds to aldehydes.…
TADDOLs with Unprecedented Helical Twisting Power in Liquid Crystals. Preliminary communication
- H. Kuball, Bernhard Weiss, A. Beck, D. Seebach
- Chemistry
- 15 December 1997
A large number of TADDOL (α,α,α′, α′-tetraaryl-1,3-dioxolan-4,5-dimethanol) derivatives has been tested as chiral dopants for inducing conversion of nematic to cholesteric phases. With the Merck…
Direct Degradation of the Biopolymer Poly[(R)‐3‐Hydroxybutyric Acid] to (R)‐3‐Hydroxybutanoic Acid and its Methyl Ester
- D. Seebach, A. Beck, R. Breitschuh, Kurt Job
- Biology
- 28 April 2003
Direct degradation of the biopolymer poly[(R)-3-hydroxybutyric acid] to (R)-3-hydroxybutanoic acid and its methyl ester
product: (R)-(−)-methyl 3-hydroxybutanoate
product:…
Some recent advances in the use of titanium reagents for organic synthesis
- D. Seebach, A. Beck, M. Schiess, L. Widler, A. Wonnacott
- Chemistry
- 1 January 1983
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