A study of the reaction of cis-[PdRf2(AsPh3)2] (Rf = 3,5-C6Cl2F3) with ISnBu3 (that is the reversal of the natural Stille reaction of [PdRfI(AsPh3)2] with RfSnBu3) allows for the observation of cis-[PdRf2(AsPh3)(ISnBu3)], the expected intermediate from a cyclic transmetalation in the direct Stille reaction, thus providing experimental support to the operation of cyclic transmetalation pathways.
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http://dx.doi.org/10.1021/ja802994v | DOI Listing |
J Org Chem
January 2025
Laboratory of Bioorganic Chemistry and Chemical Biology, Center for Nanotechnology, Heisenbergstrasse 11, 48149 Münster, Germany.
Xanthine nucleosides play a significant role in the expansion of the four-letter genetic code. Herein, 7-functionalized 8-aza-7-deazaxanthine ribo- and 2'-deoxyribonucleosides are described. 2-Amino-6-alkoxy nucleosides were converted to halogenated 8-aza-7-deazaxanthine nucleosides by deamination followed by hydroxy/alkoxy substitution.
View Article and Find Full Text PDFOrg Lett
December 2024
School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 101408, China.
An isomerized bithiazole imide (iBTzI) acceptor was effectively synthesized and functionalized via Suzuki or Stille coupling reactions. Compared with the isomerized bithiophene imide (iBTI) and bithiazole imide (BTzI), iBTzI has a more planar skeleton. Furthermore, the conjugated skeleton of iBTzI can be extended by hydrogen and chalcogen bonds.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Due to their defined structure and large molecular size, giant molecular acceptors (GMAs) have achieved significant progress in device efficiency and stability for organic solar cells. Unlike the classical synthesis of GMAs by Stille coupling, which still suffers from high cost and lack of environmental sustainability, this work develops three GMAs metal-free catalyzed reactions. By introducing varying quantities of malononitrile groups into the linker, the optoelectric properties of GMAs can be significantly regulated.
View Article and Find Full Text PDFAcc Chem Res
December 2024
College of Textiles & Clothing, State Key Laboratory of Bio-fibers and Eco-textiles, Qingdao University, Qingdao 266071, China.
ACS Omega
November 2024
School of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand.
The synthesis of the spirocyclic imine fragment of the portimine family of marine toxins has been achieved. A densely functionalized key lactone-ester intermediate was assembled via a highly diastereoselective Diels-Alder cycloaddition, involving a novel γ-hydroxymethyl-α,β-butenolide dienophile. A Stille coupling was employed to install the vinyl group.
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