2020-58-8Relevant academic research and scientific papers
3,6-Dibenzoxyl-1,2-pyridazine: A new versatile benzoyl transferring agent for NH2, -OH and -SH benzoylations
Mashraqui, Sabir Hussain,Shivaji, Jadhav Latika
, p. 927 - 935 (2007/10/03)
A newly synthesized 3,6-dibenzoxyl-1,2-pyridazine 3 has been investigated for its potential to transfer the benzoyl group to various organic substrates carrying -NH2, -OH and -SH groups. The benzoyl transfer is fairly general in scope, occurs under convenient conditions and provides good to excellent yields of benzoylated products. Moreover, by choosing proper conditions, it is possible to achieve chemoselective benzoylation in bi-functional molecules. For instance, N-benzoylation of aromatic amines can be selectively accomplished over that of aliphatic amines and vice versa by manipulating reaction conditions. Selective N- or O-benzoylation in aminophenols is also possible. Although, not studied in detail, we final that dibenzoate 3 can also be used to effect C-benzoylation of reactive phenols and ketones, as exemplified by the C-benzoylation of resorcinol and acetophenone, respectively. Dibenzoate 3, besides being a crystalline, easy to handle, solid possesses twice the potential as an acyl carrier compared to the other known acyl carriers. These features make 3 as an attractive choice for many applications pertaining to benzoyl transfer reactions.
Synthesis of new 2,5-substituted 1,3-oxathiolanes. Intermediates in nucleoside chemistry
Kraus,Attardo
, p. 1046 - 1048 (2007/10/02)
A synthetic approach for new 2-hydroxymethyl-5-ethoxy-1,3-oxathiolane derivatives is described. These heterocyclic five membered rings are suitably substituted to be potential sugar candidates in nucleoside chemistry.
