Optical Studies of Poly(hydroxy imide) to Polybenzoxazole Thermal Rearrangement.
- Published in:
- Macromolecular Chemistry & Physics, 2015, v. 216, n. 24, p. 2377, doi. 10.1002/macp.201500200
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- Article
Works matching DE "COPE rearrangement"
Results: 15
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Gold-Catalyzed Tandem Cycloisomerization/Cope Rearrangement: An Efficient Access to the Hydroazulenic Motif.
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- Angewandte Chemie, 2013, v. 125, n. 34, p. 9184, doi. 10.1002/ange.201304497
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- Article
3
BET & ELF Quantum Topological Analysis of Neutral 2-Aza-Cope Rearrangement of γ-Alkenyl Nitrones.
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- Molecules, 2017, v. 22, n. 8, p. 1371, doi. 10.3390/molecules22081371
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- Article
4
A DFT study of solvent effects on the kinetics and mechanism of the [3,3] hetero-Cope rearrangement of 1-butene thiobenzoate.
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- Progress in Reaction Kinetics & Mechanism, 2016, v. 41, n. 2, p. 153, doi. 10.3184/146867816X14634977847625
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- Article
5
An Organocatalytic Cope Rearrangement.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 38, p. 11557, doi. 10.1002/anie.201606480
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- Article
6
Rhodium-Catalyzed Tandem Cyclopropanation/Cope Rearrangement of 4-Alkenyl-1-sulfonyl-1,2,3-triazoles with Dienes.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 38, p. 10044, doi. 10.1002/anie.201304310
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- Article
7
Quantum-chemical study of barbaralone in singlet and triplet states.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 3, p. 589, doi. 10.1134/S107036321503010X
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- Article
8
Cope Rearrangement in Bicyclo[5.1.0]octa-2,5-diene and its Mono- and Di-Hetero Analogues: A DFT Study.
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- Australian Journal of Chemistry, 2017, v. 70, n. 6, p. 683, doi. 10.1071/CH16488
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9
A gold-catalysed enantioselective Cope rearrangement of achiral 1,5-dienes.
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- Nature Chemistry, 2012, v. 4, n. 5, p. 405, doi. 10.1038/nchem.1327
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- Article
10
N-heteroatom substitution effect in 3-aza-cope rearrangements.
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- Chemistry Central Journal, 2013, v. 7, n. 1, p. 1, doi. 10.1186/1752-153X-7-94
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- Article
11
An Organocatalytic Cope Rearrangement.
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- Angewandte Chemie, 2016, v. 128, n. 38, p. 11729, doi. 10.1002/ange.201606480
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- Article
12
Rearrangements in the mechanisms of the indole alkaloid prenyltransferases.
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- Pure & Applied Chemistry, 2013, v. 85, n. 10, p. 1935, doi. 10.1351/PAC-CON-13-02-02
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- Article
13
Probing the Fluxional Bonding Nature of Rapid Cope rearrangements in Bullvalene C<sub>10</sub>H<sub>10</sub> and Its Analogs C<sub>8</sub>H<sub>8</sub>, C<sub>9</sub>H<sub>10</sub>, and C<sub>8</sub>BH<sub>9</sub>.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-53488-5
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14
Laser control in open quantum systems: preliminary analysis toward the Cope rearrangement control in methyl-cyclopentadienylcarboxylate dimer.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2012, v. 131, n. 6, p. 1, doi. 10.1007/s00214-012-1236-5
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15
Competitive Gold-Promoted Meyer-Schuster and oxy-Cope Rearrangements of 3-Acyloxy-1,5-enynes: Selective Catalysis for the Synthesis of (+)-( S)-γ-Ionone and (−)-(2 S,6 R)- cis-γ-Irone.
- Published in:
- Chemistry - A European Journal, 2015, v. 21, n. 40, p. 14068, doi. 10.1002/chem.201502382
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- Article