72423-57-5Relevant articles and documents
New method for the synthesis of pyrromethanes
Okada, Kunisuke,Saburi, Kiyoshi,Nomura, Keishi,Tanino, Hideo
, p. 2127 - 2131 (2007/10/03)
Coupling reaction of 2-mercaptobenzothiazolylmethylpyrrole with α-free pyrrole in the presence of silver(I) triflate proceeds smoothly at room temperature to give a pyrromethane in excellent yield. The azafulvenium ion, an active form that reacts with α-f
On the Mechanism of Porphobilinogen Deaminase. Design, Synthesis, and Enzymatic Reactions of Novel Porphobilinogen Analogs.
Pichon, Clotilde,Clemens, Karen R.,Jacobson, Alan R.,Scott, A. Ian
, p. 4687 - 4712 (2007/10/02)
Three new derivatives of porphobilinogen (PBG; 1) were designed and synthesized to study the mechanism of ammonia loss during the tetramerization of PBG, catalyzed by the PBG deaminase.Two of these compounds are substituted at the C-11 carbon with CH3 or
Biosynthesis of Porphyrins and Related Macrocycles. Part 17. Chemical and Enzymic Transformation of Isomeric Aminomethylbilanes into Uroporphyrinogens: Proof that Unrearranged Bilane is the Preferred Enzymic Substrate and Detection of a Transient Intermed
Battersby, Alan R.,Fookes, Christopher J. R.,Gustafson-Potter, Kerstin E.,McDonald, Edward,Matcham, George W. J.
, p. 2413 - 2426 (2007/10/02)
Six isomeric aminomethylbilanes have been built by unambiguous synthesis.One bilane has the unrearranged structure corresponding to straightforward head-to-tail assembly of four units of porphobilinogen; the other five bilanes have one or more of the pyrr
