The chemistry of 1,6-dioxapyrenes part 3 : Scope and limitations of an acid catalyzed ring-closing reaction
Author:
Publisher
Wiley
Subject
Organic Chemistry
Reference23 articles.
1. Molecular structures, electronic spectra, and aromaticity of 1,6- and 1,8-dioxa analogues of pyrene and benzo[a]pyrene. Semiempirical molecular orbital calculations
2. Electrical and magnetic properties of the new conductors: (TMDTP)2 AsF6 and (TMDOP)2 AsF6
3. Novel peri-condensed Weitz-type donors: synthesis, physical properties, and crystal structures of 3,10-dithiaperylene (DTPR), 1,6-dithiapyrene (DTPY), and some of their CT complexes
4. Dimensionality Of Stacked Organic Conductors. A New One Dimensional Material: 1 6-Dithiapyrene-Tcnq
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1. A new donor for charge-transfer systems: synthesis and properties of 2,4,7,9-tetramethyl-1,6-dithiapyrene (TMDTP) and structure of (TMDTP)3(PF6)2·2THF and TMDTP–TCNQ;RSC Advances;2021
2. Iridium-Catalyzed Tandem Cyclization of Benzoylacetonitriles with Diazo Compounds Leading to Substituted Naphtho[1,8-bc ]pyrans by Sequential C−H Functionalization;Advanced Synthesis & Catalysis;2018-04-19
3. Hydroxyl-Directed Rhodium-Catalyzed C−H Bond Activation and Cyclization Leading to Naphtho[1,8-bc ]pyran Derivatives and its Analogues;Advanced Synthesis & Catalysis;2018-04-14
4. Construction of (Dihydro)naphtho[1,8-bc]pyrans via Rh(III)-Catalyzed Twofold C–H Activation of Benzoylacetonitriles;Organic Letters;2018-04-02
5. Tert-butylation of naphthalene-2,6-diol and 6-methoxynaphthalen-2-ol;Arkivoc;2017-08-23
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