Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

A new class of polycyclic aromatic hydrocarbons--oligoindenopyrenes--has been synthesized featuring a Pd-catalyzed Suzuki-Heck coupling cascade. The oligoindenopyrenes are robust, highly colored substructures of C(70) and have properties that might prove useful in new organic materials or devices. After excitation, the tetraindenopyrene derivative 3d undergoes efficient deactivation (99%) by internal conversion to the ground state. The small fluorescence quantum yield (0.004) is in accordance with the short (0.6 ns) fluorescence decay time.

Download full-text PDF

Source
http://dx.doi.org/10.1021/jo0613939DOI Listing

Publication Analysis

Top Keywords

class polycyclic
8
oligoindenopyrenes class
4
polycyclic aromatics
4
aromatics class
4
polycyclic aromatic
4
aromatic hydrocarbons--oligoindenopyrenes--has
4
hydrocarbons--oligoindenopyrenes--has synthesized
4
synthesized featuring
4
featuring pd-catalyzed
4
pd-catalyzed suzuki-heck
4

Similar Publications

Studies toward the synthesis of yaretol: an unexpected rearrangement en route to the tricyclic core.

Tetrahedron

June 2025

Department of Chemistry, Vanderbilt University, 7330 Stevenson Center, Nashville, Tennessee 37235, United States.

Yaretol is a polycyclic norditerpene constituting a structurally distinct class of terpene natural products isolated from which, to date, has not been accessed via total synthesis. Herein, we report our synthetic efforts toward a key intramolecular Diels-Alder furan (IMDAF) cycloaddition to construct the carbon framework. We discuss our efforts toward the cycloaddition wherein undesired aromatization and unanticipated rearrangement of the cycloadduct are observed.

View Article and Find Full Text PDF

dos Santos, JM, Kennedy, T, Zhu, J, McPike, A, Ray, M, Demirci, J, and Dechant, J. Sex-specific adverse association of endocrine disrupting chemicals on peak anaerobic power and skeletal muscle mass of active young adults. J Strength Cond Res XX(X): 000-000, 2025-Endocrine disrupting chemicals, such as bisphenol A (BPA) and bisphenol S (BPS), and polycyclic aromatic hydrocarbons (PAHs) are a broad class of industrial compounds that induce adverse physiologic outcomes dependent on biologic sex.

View Article and Find Full Text PDF

Environmental xenobiotics comprising a wide array of natural and synthetic chemicals are an escalating global health concern due to their persistent presence in ecosystems and their profound impact on human liver health. The liver, as the body's principal detoxification organ, is especially vulnerable to these substances, which are commonly encountered through ingestion, inhalation, or dermal exposure. This review systematically categorizes key classes of environmental xenobiotics, including aflatoxins, alcohol, polychlorinated biphenyls (PCBs), per- and polyfluoroalkyl substances (PFAS), polycyclic aromatic hydrocarbons (PAHs), pesticides, heavy metals, bisphenol A (BPA), aristolochic acids, cyanotoxins, and nitrosamines, based on their sources and chemical properties.

View Article and Find Full Text PDF

Isolation, biosynthesis, and biological activity of pradimicins from actinomycetes.

Bioorg Chem

August 2025

Tropical Crops Genetic Resources Institute, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China; Key Laboratory of Biology and Cultivation of Herb Medicine (Haikou), Ministry of Agriculture and Rural Affairs, Haikou 571101, China; Key Laboratory of Tropical Crops Germplasm Resour

Pradimicins are a class of angular polycyclic compounds characterized by a benzo[α]naphthacenequinone core substituted with a d-amino acid and a hexose sugar. Since their discovery in 1988, approximately 51 pradimicin analogs have been identified from natural sources. These compounds are biosynthesized by type II polyketide synthases and exhibit a wide range of biological activities.

View Article and Find Full Text PDF

Divergent Synthesis of and Structurally Related Monoterpenoid Indole Alkaloids: A Non-biomimetic Strategy.

Acc Chem Res

September 2025

Key Lab of Functional Molecular Engineering of Guangdong Province, School of Chemistry & Chemical Engineering, South China University of Technology, Guangzhou, Guangdong 510641, China.

ConspectusMonoterpenoid indole alkaloids constitute one of the largest natural product families, with over 3000 members reported to date. , a genus of about 30 species, is notable for its rich alkaloid diversity. These plants produce unique monoterpenoid indole alkaloids with intriguing structures and bioactive properties, making them a key focus in synthetic chemistry research over the years.

View Article and Find Full Text PDF