Head-to-Tail Dimerization and Organogelating Properties of Click Peptidomimetics
摘要:
Click triazole-based ollgopeptides 1-3 were found to self-dimerize (K-dim approximate to 10-680 M-1) In a head-to-tail fashion based on H-1 variable concentration, 2D, and HID exchange NMR, VPO, CD, FT-IR studies and Gaussian 03 simulations. The dimerization constant K-dim was shown to increase with increasing number of the amino acid units. Within the same oligomeric series, the K-dim, value is strongly affected by the size of the C-terminal end group. The tripeptides 2 are also excellent organogelators of aromatic solvents.
Expansion of Phosphane Treasure Box for Staudinger Peptide Ligation
作者:Kiran Bajaj、Girinath G. Pillai、Rajeev Sakhuja、Dalip Kumar
DOI:10.1021/acs.joc.0c01319
日期:2020.10.2
A smooth traceless ligation strategy using an air-stable phosphane probe (2-(diphenylphosphanyl)phenyl)methanol as a C-terminus activator has been demonstrated at simple and sterically hindered amino acid junctions (Gly, Ala, Trp, Glu). This Staudinger peptide ligation proceeds via formation of a seven-membered transition state to afford di-, tetra-, and pentapeptides in 78–95% yields. The experimental
Carboxylate-Assisted Iridium-Catalyzed C−H Amination of Arenes with Biologically Relevant Alkyl Azides
作者:Tao Zhang、Xuejiao Hu、Zhen Wang、Tiantian Yang、Hao Sun、Guigen Li、Hongjian Lu
DOI:10.1002/chem.201504880
日期:2016.2.24
wide substrate scope is reported. Benzamides with electron‐donating and ‐withdrawing groups and linear, branched, and cyclic alkyl azides are all applicable. Cesium carboxylate is crucial for both reactivity and regioselectivity of the reactions. Many biologically relevant molecules, such as amino acid, peptide, steroid, sugar, and thymidine derivatives can be introduced to arenes with high yields and
Benzotriazol-1-yl-sulfonyl Azide for Diazotransfer and Preparation of Azidoacylbenzotriazoles
作者:Alan R. Katritzky、Mirna El Khatib、Oleg Bol’shakov、Levan Khelashvili、Peter J. Steel
DOI:10.1021/jo101296s
日期:2010.10.1
Benzotriazol-1-yl-sulfonyl azide, a new crystalline, stable, and easily available diazotransfer reagent provides N-(α-azidoacyl)benzotriazoles convenient for N-, O-, C- and S-acylations. The efficient syntheses of various amides, azido protected peptides, esters, ketones and thioesters is reported together with a wide range of azides (including α-azido acids from α- amino acids in partially aqueous conditions) and
Small molecule microarray-facilitated screening of affinity-based probes (AfBPs) for γ-secretase
作者:Haibin Shi、Kai Liu、Ashley Xu、Shao Q. Yao
DOI:10.1039/b910611a
日期:——
A small molecule microarray (SMM) platform is developed herein, which enables high-throughput discovery of affinity-based probes (AfBPs) against γ-secretase.
An Efficient, Inexpensive, and Shelf-Stable Diazotransfer Reagent: Imidazole-1-sulfonyl Azide Hydrochloride
作者:Ethan D. Goddard-Borger、Robert V. Stick
DOI:10.1021/ol701581g
日期:2007.9.1
The design and synthesis of a new diazotransfer reagent, imidazole-1-sulfonyl azide hydrochloride, are reported. This reagent has proven to equal triflyl azide in its ability to act as a "diazo donor" in the conversion of both primary amines into azides and activated methylene substrates into diazo compounds. Crucially, this reagent can be prepared in a one-pot reaction on a large scale from inexpensive