We developed a general method for the selective photochemical homo- and heterodimerization of cinnamic acid derivatives with the use of commercially available 1,8-dihydroxynaphthalene as a covalent template. A variety of symmetrical and unsymmetrical β-truxinic acids were obtained in high yields and as single diastereomers. The use of a template not only provides the alignment of the two olefins with suitable proximity (<4.2 Å) but also allows the heterodimerization of two different cinnamic acids, leading to unsymmetrical β-truxinic acid products.
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http://dx.doi.org/10.1021/acs.joc.1c01534 | DOI Listing |
J Org Chem
September 2021
Department of Chemistry, Faculty of Science, Bilkent University, Ankara, Ankara 06800, Turkey.
We developed a general method for the selective photochemical homo- and heterodimerization of cinnamic acid derivatives with the use of commercially available 1,8-dihydroxynaphthalene as a covalent template. A variety of symmetrical and unsymmetrical β-truxinic acids were obtained in high yields and as single diastereomers. The use of a template not only provides the alignment of the two olefins with suitable proximity (<4.
View Article and Find Full Text PDFChem Commun (Camb)
March 2020
State Key Lab of Transducer Technology, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050, P. R. China.
We developed ultrathin dual-mesoporous polymer nanosheets by combining co-assembly of different templates with in situ synthesis of functional polymers, which featured inherent smaller and template-directed larger mesopores (2.6 nm and 15 nm, respectively), ultrathin nanolayers (20 nm), high surface area (268 m2 g-1), intrinsic fluorescent properties and effective detectability for organophosphates.
View Article and Find Full Text PDFOrg Biomol Chem
November 2016
Department of Molecular Design and Engineering, Graduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya 464-8603, Japan.
The photoirradiation of 9-phenylethynylanthracene in degassed chloroform and benzene afforded not only a [4 + 2]-anti Diels-Alder addition dimer, but also a [4 + 4]-anti-dimer as a minor product for the first time as revealed by single-crystal X-ray analysis, while the anthracene residue was quantitatively oxidised in undegassed dilute chloroform, giving the corresponding endoperoxides. The photochemical reactions of carboxylic acid monomers bearing a 9-phenylethynylanthracene unit at one and both ends were further investigated in the presence and absence of the complementary amidine dimer as the template. It was found that a similar photooxidation reaction of the monomers was significantly suppressed in the presence of the template even in undegassed chloroform.
View Article and Find Full Text PDFOrg Biomol Chem
July 2015
Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079, PR China.
Mechanically interlocked structures such as rotaxanes and catenanes provide a novel backbone for constructing functional materials with unique structural characteristics. In this study, we have designed and synthesized a series of photoswitchable rotaxanes and catenanes containing photochromic dithienylethene fragments using a template-directed clipping approach based on dynamic imine chemistry. Their structures have been confirmed using NMR, mass spectrometry and elemental analysis.
View Article and Find Full Text PDFOrg Lett
February 2013
Department of Chemistry, Pondicherry University, Puducherry 605 014, India.
The concept of using a product of a template-directed solid-state reaction as a template is demonstrated. A cyclobutane lined with four carboxylic acid groups is employed as the template in photoreactive cocrystals. The resulting material is shown to exhibit polymorphism.
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