Cargando…

Retraction: Beltaïef et al. An Expeditious Synthesis of [1,2]Isoxazolidin-5-ones and [1,2]Oxazin-6-ones from Functional Allyl Bromide Derivatives. Molecules 2010, 15, 4094-4101

Detalles Bibliográficos
Autor principal:	Rittman, Martyn
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2014
Materias:	Retraction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271862/ https://www.ncbi.nlm.nih.gov/pubmed/25329873 http://dx.doi.org/10.3390/molecules191016810

Ejemplares similares

An Expeditious Synthesis of [1,2]Isoxazolidin-5-ones and [1,2]Oxazin-6-ones from Functional Allyl Bromide Derivatives
por: Beltaïef, Imen, et al.
Publicado: (2010)

Gold-catalyzed oxycyclization of allenic carbamates: expeditious synthesis of 1,3-oxazin-2-ones
por: Alcaide, Benito, et al.
Publicado: (2013)

1-Phenyl-1H-naphtho[1,2-e][1,3]oxazin-3(2H)-one
por: Gondal, Humaira Y., et al.
Publicado: (2010)

4094 Structural Determinants of Immunogenicity for Peptide-Based Immunotherapy
por: Devlin, Jason, et al.
Publicado: (2020)

(±)-2′-Phenylcyclohexanespiro-4′-(azepano[1,2-b]isoxazolidine)
por: Crimmins, Daryl, et al.
Publicado: (2008)

Iodination of carbohydrate-derived 1,2-oxazines to enantiopure 5-iodo-3,6-dihydro-2H-1,2-oxazines and subsequent palladium-catalyzed cross-coupling reactions
por: Medvecký, Michal, et al.
Publicado: (2016)

[3+3]-Annulation of Cyclic Nitronates with Vinyl Diazoacetates: Diastereoselective Synthesis of Partially Saturated [1,2]Oxazino[2,3-b][1,2]oxazines and Their Base-Promoted Ring Contraction to Pyrrolo[1,2-b][1,2]oxazine Derivatives
por: Antonova, Yulia A., et al.
Publicado: (2023)

One-pot synthesis of naphtho[1,2-e][1,3]oxazines in the presence of FNAOSiPAMP*/Cu(II) as an almond shell based nanocatalyst
por: Keihanfar, Mina, et al.
Publicado: (2022)

Carbohydrate-auxiliary assisted preparation of enantiopure 1,2-oxazine derivatives and aminopolyols
por: Jasiński, Marcin, et al.
Publicado: (2012)

1-Allyl-2-aminopyridin-1-ium bromide
por: Seethalakshmi, T., et al.
Publicado: (2013)

3-Methyl-1H-pyrrolo[2,1-c][1,4]oxazin-1-one
por: Khan, Salman Tariq, et al.
Publicado: (2010)

3-Phenyl-1H-pyrrolo[2,1-c][1,4]oxazin-1-one
por: Khan, Salman Tariq, et al.
Publicado: (2010)

Efficient and stereoselective one-pot synthesis of benzo[b]oxazolo[3,4-d][1,4]oxazin-1-ones
por: Zhao, Hongyi, et al.
Publicado: (2020)

Palladium-catalyzed cross coupling reactions of 4-bromo-6H-1,2-oxazines
por: Zimmer, Reinhold, et al.
Publicado: (2009)

Solid-Phase Synthesis of ɤ-Lactone and 1,2-Oxazine Derivatives and Their Efficient Chiral Analysis
por: Krupkova, Sona, et al.
Publicado: (2016)

Inhibition of HIV-1 Replication by Isoxazolidine and Isoxazole Sulfonamides
por: Loh, Belinda, et al.
Publicado: (2010)

4-Allylmorpholin-4-ium bromide
por: Han, Meng Ting
Publicado: (2012)

1-Allyl-3-phenylquinoxalin-2(1H)-one
por: Benzeid, Hanane, et al.
Publicado: (2011)

Synthesis of spiro[isoindole-1,5’-isoxazolidin]-3(2H)-ones as potential inhibitors of the MDM2-p53 interaction
por: Giofrè, Salvatore V, et al.
Publicado: (2016)

1-Allyl-3,3-diphenylindolin-2-one
por: Nirmala, S., et al.
Publicado: (2008)

A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core
por: Cowper, Nicholas G. W., et al.
Publicado: (2020)

Gum arabic-OPO(3)H(2) as a new natural-based green catalyst for the one-pot pseudo-four-component synthesis of naphtho[1,2-e][1,3]oxazines
por: Hosseinikhah, Sahar Saadat, et al.
Publicado: (2020)

4-Benzyl-7-chloro-2H-1,4-benzoxazin-3(4H)-one
por: Li, Zhu-Bo, et al.
Publicado: (2009)

2-Butyl-1,3-diphenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine
por: Li, Yong Hua, et al.
Publicado: (2008)

1,3-Di-3-pyridyl-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazine
por: Şen, Betül, et al.
Publicado: (2008)

2-Benzyl-1,3-diphenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine
por: Zhang, Yuan, et al.
Publicado: (2009)

8-Bromo-1,3-diphenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine
por: Jasinski, Jerry P., et al.
Publicado: (2010)

6-Allyl-8-methoxy-3-phenyl-3,4-dihydro-2H-benzo[e][1,3]oxazine
por: Zhu, Jing, et al.
Publicado: (2011)

Novel isoxazolidine analogues of homonucleosides and homonucleotides
por: Piotrowska, Dorota G., et al.
Publicado: (2016)

(E)-1,2-Bis(1-allylbenzimidazol-2-yl)ethene
por: Chen, Li-Zhuang
Publicado: (2010)

Gold-catalyzed formation of pyrrolo- and indolo-oxazin-1-one derivatives: The key structure of some marine natural products
por: Taskaya, Sultan, et al.
Publicado: (2015)

1,2-Metallate Rearrangement as a Toolbox for the Synthesis of Allylic Alcohols
por: Linne, Yannick, et al.
Publicado: (2023)

One-Pot Chemoenzymatic Cascade for the Enantioselective C(1)-Allylation of Tetrahydroisoquinolines
por: Sangster, Jack J., et al.
Publicado: (2023)

1-Allyl-1H-1,3-benzimidazol-2(3H)-one
por: Belaziz, Dounia, et al.
Publicado: (2012)

DMSO–allyl bromide: a mild and efficient reagent for atom economic one-pot N-allylation and bromination of 2°-aryl amines, 2-aryl aminoamides, indoles and 7-aza indoles
por: Smile, Suresh Snoxma, et al.
Publicado: (2022)

Tris(allylthiourea-κS)bromidozinc(II) bromide
por: Sun, Hai-Qing, et al.
Publicado: (2011)

Oligonucleotide nanoassemblies with allyl bromide scaffold-based small molecules
por: Abbas, Sk Jahir, et al.
Publicado: (2023)

Novel Isoxazolidine and γ-Lactam Analogues of Homonucleosides
por: Piotrowska, Dorota G., et al.
Publicado: (2019)

Identification of a novel 1,2 oxazine that can induce apoptosis by targeting NF-κB in hepatocellular carcinoma cells
por: Somu, Chaithanya, et al.
Publicado: (2020)

1,3-Oxazin-6-one Derivatives and Bohemamine-Type Pyrrolizidine Alkaloids from a Marine-Derived Streptomyces spinoverrucosus
por: Fu, Peng, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_q8nq1170nhejr35ftdir8ra3jh