Cover Picture: Nanographene – A Scaffold of Two‐Dimensional Materials (Chem. Rec. 3/2022).
- Published in:
- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202280301
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- Article
Works matching IS 15278999 AND DT 2022 AND VI 22 AND IP 3
Results: 12
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2
Desymmetrisation of meso‐2,4‐Dimethyl‐8‐oxabicyclo[3.2.1]‐oct‐6‐ene‐3‐ol and its Application in Natural Product Syntheses.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100286
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- Article
3
Synthesis of Pyrrolidine‐ and γ‐Lactam‐Containing Natural Products and Related Compounds from Pyrrole Scaffolds.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100277
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- Article
4
Recent Advances in the High‐Valent Cobalt‐Catalyzed C−H Functionalization of N‐Heterocycles.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100271
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- Article
5
Recent Trends in Synthesis and Applications of Porous MXene Assemblies: A Topical Review.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100261
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- Article
6
Nanographene – A Scaffold of Two‐Dimensional Materials.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100257
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- Article
7
Polyanionic Imido‐P(V) Ligands: From Transition Metal Complexes to Coordination Driven Self‐Assemblies.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100281
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- Article
8
Sleeping Beauties in Chemistry. Oosterhoff, Havinga and Schlatmann: Four Years Before "The Woodward‐Hoffmann Rules"<sup>†</sup>**.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100245
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- Article
9
Advances of Sulfenate Anions in Catalytic Asymmetric Synthesis of Sulfoxides.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100242
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- Article
10
Ortho C−H Functionalization of 2‐Arylimidazo[1,2‐a]pyridines.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100240
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- Article
11
Process Intensification of Enzymatic Synthesis of Flavor Esters: A Review.
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- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100213
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- Article
12
Multicomponent Reactions (MCRs) with o‐Quinone Methides.
- Published in:
- Chemical Record, 2022, v. 22, n. 3, p. 1, doi. 10.1002/tcr.202100251
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- Article