115842-38-1Relevant articles and documents
Synthesis of bis-pyrrole tetra esters and alcohols as novel mimetics of the anticancer mitomycin
Abdulla, Zubair M.,Iyer, Radhakrishnan P.,Akamanchi, Krishnamachari G.,Degani, Mariam S.,Coutinho, Evans C.
experimental part, p. 38 - 49 (2011/03/21)
Open-chain bis-Reissert compounds 1 were converted to the corresponding bis-oxazolium intermediates via acid-catalyzed intramolecular cyclization. These oxazolium compounds exist in a variety of tautomeric structures in which the meso-ionic form can be in
Synthesis of a Bis-α-amino Acid
Iyer, Radhakrishnan P.,Lawate, Saurabh S.,Sonaseth, Mariam S.
, p. 3 - 4 (2007/10/02)
A double Strecker reaction has provided a novel route to a bis-α-amino acid.In analogy with the behaviour of open-chain Reissert compounds, 5, a dibenzoyl derivative of bis-aminonitrile (4) undergoes a facile anchimerically-assisted transformation to 2.
