Asymmetric Synthesis of Carboranyl Amino Acids with Potential Use in BNCT
- 1 January 1993
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- A general, convenient way to carborane-containing amino acids for boron neutron capture therapyTetrahedron Letters, 1992
- Novel carboranyl amino acids and peptides: reagents for antibody modification and subsequent neutron-capture studiesBioconjugate Chemistry, 1991
- Asymmetric synthesis of α-amino acids and α-N-hydroxyamino acids via electrophilic amination of bornanesultam-derived enolates with 1-chloro-1-nitrosocyclohexane.Tetrahedron Letters, 1990
- Asymmetric alkylations of a sultam-derived glycinate equivalent: practical preparation of enantiomerically pure α-amino acidsTetrahedron Letters, 1989
- Resolution and use in α-amino acid synthesis of imidazolidinone glycine derivativesTetrahedron, 1988
- Determination ofD-amino acids. II. Use of a bifunctional reagent, 1,5-difluoro-2,4-dinitrobenzeneCarlsberg Research Communications, 1984
- The Synthesis of [4‐Carboranylalanine, 5‐Leucine]‐Enkephalin (Including an Improved Preparation of t‐Butoxycarbonyl‐L‐o‐carboranylalnine, New Derivatives of L‐Propargylglycine, and a Note on Melanotropic and Opiate Receptor Binding Characteristics)Helvetica Chimica Acta, 1979
- Synthesis of angiotensins, bradykinins and substance P octapeptides in which the residues Phe and Tyr have been replaced with car and of [Car1, Leu5]‐enkephalinHelvetica Chimica Acta, 1979
- Hormone‐Receptor Interactions. Carboranylalanine (Car) as a Phenylalanine Analogue: Reactions with ChymotrypsinHelvetica Chimica Acta, 1977
- L‐o‐Carboranylalanine, a Boron Analogue of PhenylalanineHelvetica Chimica Acta, 1976