Arrieta A - Search Results

1

Higher-Order Electrocyclizations in Biological and Synthetic Processes.

de Cózar A, Arrieta A, Arrastia I, Cossío FP. de Cózar A, et al. Among authors: arrieta a. Chempluschem. 2023 Nov;88(11):e202300482. doi: 10.1002/cplu.202300482. Epub 2023 Oct 10. Chempluschem. 2023. PMID: 37753849 Review.

2

New insights on the origins of the stereocontrol of the staudinger reaction: [2 + 2] cycloaddition between ketenes and N-silylimines.

Arrieta A, Cossío FP, Lecea B. Arrieta A, et al. J Org Chem. 2000 Dec 15;65(25):8458-64. doi: 10.1021/jo0007736. J Org Chem. 2000. PMID: 11112564

3

Direct evaluation of secondary orbital interactions in the Diels-Alder reaction between cyclopentadiene and maleic anhydride.

Arrieta A, Cossío FP, Lecea B. Arrieta A, et al. J Org Chem. 2001 Sep 7;66(18):6178-80. doi: 10.1021/jo0158478. J Org Chem. 2001. PMID: 11529749 No abstract available.

4

Solvent and Substituent Effects in the Periselectivity of the Staudinger Reaction between Ketenes and alpha,beta-Unsaturated Imines. A Theoretical and Experimental Study.

Lecea B, Arrastia I, Arrieta A, Roa G, Lopez X, Arriortua MI, Ugalde JM, Cossío FP. Lecea B, et al. Among authors: arrieta a. J Org Chem. 1996 May 3;61(9):3070-3079. doi: 10.1021/jo951867w. J Org Chem. 1996. PMID: 11667169

5

Origins of the Stereodivergent Outcome in the Staudinger Reaction between Acyl Chlorides and Imines.

Arrieta A, Lecea B, Cossío FP. Arrieta A, et al. J Org Chem. 1998 Aug 21;63(17):5869-5876. doi: 10.1021/jo9804745. J Org Chem. 1998. PMID: 11672189

6

Competitive Mechanisms and Origins of Stereocontrol in the [2 + 2] Thermal Cycloaddition between Imines and Keteniminium Cations. A Complementary Entry to 2-Azetidinones (beta-Lactams) and Related Compounds.

Arrieta A, Cossío FP, Lecea B. Arrieta A, et al. J Org Chem. 1999 Mar 19;64(6):1831-1842. doi: 10.1021/jo9815002. J Org Chem. 1999. PMID: 11674271

7

On the mechanism of conversion of N-acyl-4-acyloxy-beta-lactams into 2-substituted 1,3-oxazin-6-ones. Can a low-barrier transition state be antiaromatic?

Alajarín M, Sánchez-Andrada P, Cossío FP, Arrieta A, Lecea B. Alajarín M, et al. Among authors: arrieta a. J Org Chem. 2001 Dec 14;66(25):8470-7. doi: 10.1021/jo015922e. J Org Chem. 2001. PMID: 11735527

8

[4+3] versus [4+2] mechanisms in the dimerization of 2-boryl-1,3-butadienes. A theoretical and experimental study.

Carreaux F, Possémé F, Carboni B, Arrieta A, Lecea B, Cossío FP. Carreaux F, et al. Among authors: arrieta a. J Org Chem. 2002 Dec 27;67(26):9153-61. doi: 10.1021/jo026491i. J Org Chem. 2002. PMID: 12492315

9

Light-induced aminocarbene to imine dyotropic rearrangement in a chromium(0) center: an unprecedented reaction pathway.

Sierra MA, Fernández I, Mancheño MJ, Gómez-Gallego M, Torres MR, Cossío FP, Arrieta A, Lecea B, Poveda A, Jiménez-Barbero J. Sierra MA, et al. Among authors: arrieta a. J Am Chem Soc. 2003 Aug 13;125(32):9572-3. doi: 10.1021/ja035614t. J Am Chem Soc. 2003. PMID: 12904007

10

Enhancing stereochemical diversity by means of microwave irradiation in the absence of solvent: synthesis of highly substituted nitroproline esters via 1,3-dipolar reactions.

Díaz-Ortiz A, de la Hoz A, Herrero MA, Prieto P, Sánchez-Migallón A, Cossío FP, Arrieta A, Vivanco S, Foces-Foces C. Díaz-Ortiz A, et al. Among authors: arrieta a. Mol Divers. 2003;7(2-4):175-80. doi: 10.1023/b:modi.0000006799.01924.2e. Mol Divers. 2003. PMID: 14870848

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