213757-66-5Relevant academic research and scientific papers
Synthesis of the side chain cross-linked tyrosine oligomers dityrosine, trityrosine, and pulcherosine
Skaff, Ojia,Jolliffe, Katrina A.,Hutton, Craig A.
, p. 7353 - 7363 (2007/10/03)
An efficient synthesis of dityrosine and the first syntheses of the tyrosine trimers trityrosine and pulcherosine have been achieved. Protected 3-iodotyrosine underwent tandem Miyaura borylation-Suzuki coupling to give protected dityrosine. The choice of
A convenient preparation of dityrosine via Miyaura borylation-Suzuki coupling of iodotyrosine derivatives
Hutton, Craig A.,Skaff, Ojia
, p. 4895 - 4898 (2007/10/03)
Dityrosine has been prepared from 3-iodo-L-tyrosine derivatives by sequential Miyaura borylation and Suzuki coupling reactions. A tandem borylation-coupling protocol results in improved yields of the dityrosine derivatives. Suitable protecting group strat
Enantioselective synthesis of nonphosphorus-containing phosphotyrosyl mimetics and their use in the preparation of tyrosine phosphatase inhibitory peptides
Burke Jr., Terrence R.,Yao, Zhu-Jun,Zhao, He,Milne, George W. A.,Wu, Li,Zhang, Zhong-Yin,Voigt, Johannes H.
, p. 9981 - 9994 (2007/10/03)
Three new L-amino acid analogues 12, 18 and 25 have been prepared in protected form suitable for incorporation into peptides by solid-phase synthesis using Fmoc protocols. These agents represent nonphosphorus- containing phosphotyrosyl (pTyr) mimetics, wh
