Cargando…

Application of the Asymmetric Pictet–Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds

Tetrahydroisoquinolines are the framework of numerous natural products predominantly alkaloids, an important and one of the most wide spread families of naturally occurring compounds in the plant kingdom. Tetrahydroisoquinolines are commonly constructed through an old reaction, the so-called Pictet–...

Descripción completa

Detalles Bibliográficos
Autores principales:	M. Heravi, Majid, Zadsirjan, Vahideh, Malmir, Masumeh
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2018
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017108/ https://www.ncbi.nlm.nih.gov/pubmed/29670061 http://dx.doi.org/10.3390/molecules23040943

Ejemplares similares

The Pictet-Spengler Reaction Updates Its Habits
por: Calcaterra, Andrea, et al.
Publicado: (2020)

The Chiral Pool in the Pictet–Spengler Reaction for the Synthesis of β-Carbolines
por: Dalpozzo, Renato
Publicado: (2016)

Synthesis of aza-quaternary centers via Pictet–Spengler reactions of ketonitrones
por: Lynch-Colameta, Tessa, et al.
Publicado: (2021)

Mild and efficient cyanuric chloride catalyzed Pictet–Spengler reaction
por: Sharma, Ashish, et al.
Publicado: (2013)

Highly Stereoselective Ugi/Pictet–Spengler Sequence
por: Zhang, Bidong, et al.
Publicado: (2022)

Synthesis of tetrahydrofuro[3,2-c]pyridines via Pictet–Spengler reaction
por: Mendogralo, Elena Y, et al.
Publicado: (2023)

A Catalytic Asymmetric Pictet–Spengler Platform as a Biomimetic Diversification Strategy toward Naturally Occurring Alkaloids
por: Scharf, Manuel J., et al.
Publicado: (2022)

Norcoclaurine Synthase: Mechanism of an Enantioselective Pictet-Spengler Catalyzing Enzyme
por: Bonamore, Alessandra, et al.
Publicado: (2010)

Applications of Friedel–Crafts reactions in total synthesis of natural products
por: Heravi, Majid M., et al.
Publicado: (2018)

Total Synthesis of the Ortho-Hydroxylated Protoberberines (S)-Govaniadine, (S)-Caseamine, and (S)-Clarkeanidine via a Solvent-Directed Pictet–Spengler Reaction
por: Horst, Brendan, et al.
Publicado: (2018)

Biomimetic Phosphate-Catalyzed Pictet–Spengler Reaction for the Synthesis of 1,1′-Disubstituted and Spiro-Tetrahydroisoquinoline Alkaloids
por: Zhao, Jianxiong, et al.
Publicado: (2019)

Application of asymmetric Sharpless aminohydroxylation in total synthesis of natural products and some synthetic complex bio-active molecules
por: Heravi, Majid M., et al.
Publicado: (2018)

Total Synthesis of 6-Hydroxymetatacarboline-d Discovered from Mycena metata via the Pictet–Spengler Reaction Followed by the Horner–Wadsworth–Emmons Reaction
por: Kumar, Deepak, et al.
Publicado: (2021)

A facile and efficient method for the synthesis of crystalline tetrahydro-β-carbolines via the Pictet-Spengler reaction in water
por: Byeon, Hong-Ju, et al.
Publicado: (2020)

Solution-Phase DNA-Compatible Pictet-Spengler Reaction Aided by Machine Learning Building Block Filtering
por: Li, Ke, et al.
Publicado: (2020)

SynBio‐SynChem Approaches to Diversifying the Pacidamycins through the Exploitation of an Observed Pictet‐Spengler Reaction
por: Cartmell, Christopher, et al.
Publicado: (2021)

Enzyme catalysed Pictet-Spengler formation of chiral 1,1'-disubstituted- and spiro-tetrahydroisoquinolines
por: Lichman, Benjamin R., et al.
Publicado: (2017)

Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst
por: Andres, Rémi, et al.
Publicado: (2022)

Inverted Binding of Non-natural Substrates in Strictosidine Synthase Leads to a Switch of Stereochemical Outcome in Enzyme-Catalyzed Pictet–Spengler Reactions
por: Eger, Elisabeth, et al.
Publicado: (2020)

Correction to “Inverted Binding of Non-natural Substrates in Strictosidine Synthase Leads to a Switch of Stereochemical Outcome in Enzyme-Catalyzed Pictet–Spengler Reactions”
por: Eger, Elisabeth, et al.
Publicado: (2020)

Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate
por: Yang, Guoping, et al.
Publicado: (2021)

Uncovering the Mechanism of Azepino‐Indole Skeleton Formation via Pictet–Spengler Reaction by Strictosidine Synthase: A Quantum Chemical Investigation
por: Mou, Mingqi, et al.
Publicado: (2023)

Copper-free Sonogashira cross-coupling reactions: an overview
por: Mohajer, Fatemeh, et al.
Publicado: (2021)

The ethoxycarbonyl group as both activating and protective group in N-acyl-Pictet–Spengler reactions using methoxystyrenes. A short approach to racemic 1-benzyltetrahydroisoquinoline alkaloids
por: Keller, Marco, et al.
Publicado: (2021)

Mechanism and origins of selectivity in the enantioselective oxa-Pictet–Spengler reaction: a cooperative catalytic complex from a hydrogen bond donor and chiral phosphoric acid
por: Maskeri, Mark A., et al.
Publicado: (2020)

Prescribed drugs containing nitrogen heterocycles: an overview
por: Heravi, Majid M., et al.
Publicado: (2020)

Imaging Evaluation of 5HT(2C) Agonists, [(11)C]WAY-163909 and [(11)C]Vabicaserin, Formed by Pictet–Spengler Cyclization
por: Neelamegam, Ramesh, et al.
Publicado: (2014)

Synthesis of indole derivatives as prevalent moieties present in selected alkaloids
por: Heravi, Majid M., et al.
Publicado: (2021)

Applications of Cu(0) encapsulated nanocatalysts as superior catalytic systems in Cu-catalyzed organic transformations
por: Heravi, Majid M., et al.
Publicado: (2020)

Silver nanoparticles-decorated Preyssler functionalized cellulose biocomposite as a novel and efficient catalyst for the synthesis of 2-amino-4H-pyrans and spirochromenes
por: Saneinezhad, Sara, et al.
Publicado: (2020)

Samarium(ii) iodide-mediated reactions applied to natural product total synthesis
por: Heravi, Majid. M., et al.
Publicado: (2022)

Application of Pauson–Khand reaction in the total synthesis of terpenes
por: Heravi, Majid M., et al.
Publicado: (2021)

Ionic liquid-loaded triazine-based magnetic nanoparticles for promoting multicomponent reaction
por: Kafshdarzadeh, Kosar, et al.
Publicado: (2022)

Magnetic composite of γ-Fe(2)O(3) hollow sphere and palladium doped nitrogen-rich mesoporous carbon as a recoverable catalyst for C–C coupling reactions
por: Malmir, Masoume, et al.
Publicado: (2021)

The mitochondrial genome of the stonefly Togoperla limbata Pictet (Plecoptera: Perlidae)
por: Wang, Ying, et al.
Publicado: (2020)

Marc Auguste Pictet, 1752-1825: correspondance sciences et techniques
por: Sigrist, René
Publicado: (1996)

Direction of theoretical and experimental investigation into the mechanism of n-HA/Si-PA-SC@Ag as a bio-based heterogeneous catalyst in the reduction reactions
por: Sisakhti, Zohreh Nouripour, et al.
Publicado: (2022)

Investigation of halloysite nanotubes and Schiff base combination with deposited copper iodide nanoparticles as a novel heterogeneous catalytic system
por: Daraie, Mansoureh, et al.
Publicado: (2021)

Flow Synthesis of Biologically-Relevant Compound Libraries
por: Luque Navarro, Pilar María, et al.
Publicado: (2020)

Incorporating heterogeneous lacunary Keggin anions as efficient catalysts for solvent-free cyanosilylation of aldehydes and ketones
por: Malmir, Masoume, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_h97bg21pes1p3qvtjmsfldk73l