Cargando…

Discovery of benthol A and its challenging stereochemical assignment: opening up a new window for skeletal diversity of super-carbon-chain compounds

Super-carbon-chain compounds (SCCCs) are marine organic molecules featuring long polyol carbon chains with numerous stereocenters. Polyol–polyene compounds (PPCs) and ladder-frame polyethers (LFPs) are two major families. It is highly challenging to establish the absolute configurations of SCCCs. In...

Descripción completa

Detalles Bibliográficos
Autores principales:	Jiang, Zhong-Ping, Sun, Shi-Hao, Yu, Yi, Mándi, Attila, Luo, Jiao-Yang, Yang, Mei-Hua, Kurtán, Tibor, Chen, Wen-Hua, Shen, Li, Wu, Jun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Royal Society of Chemistry 2021
Materias:	Chemistry
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336589/ https://www.ncbi.nlm.nih.gov/pubmed/34447528 http://dx.doi.org/10.1039/d1sc02810c

Ejemplares similares

Synthesis and Stereochemical Assignment of (+)-Chamuvarinin
por: Florence, Gordon J., et al.
Publicado: (2010)

Total Synthesis and Stereochemical Assignment of (±)-Sorbiterrin A
por: Qi, Chao, et al.
Publicado: (2014)

Total Synthesis and Stereochemical Assignment of Nostosin B
por: Wang, Xiaoji, et al.
Publicado: (2017)

Enantioseparation, Stereochemical Assignment and Chiral Recognition Mechanism of Sulfoxide-Containing Drugs
por: Xiong, Fei, et al.
Publicado: (2018)

TDDFT-ECD and DFT-NMR studies of thaigranatins A–E and granatumin L isolated from Xylocarpus granatum
por: Mándi, Attila, et al.
Publicado: (2020)

Total Synthesis, Stereochemical Assignment, and Divergent Enantioselective Enzymatic Recognition of Larreatricin
por: Martin, Harry J., et al.
Publicado: (2018)

Synthesis-Driven Stereochemical Assignment of Marine Polycyclic Ether Natural Products
por: Fuwa, Haruhiko
Publicado: (2021)

Enantioselective Total Syntheses of Citrinadins A and B. Stereochemical Revision of Their Assigned Structures
por: Bian, Zhiguo, et al.
Publicado: (2014)

Stereochemical Assignment of the Protein–Protein Interaction Inhibitor JBIR-22 by Total Synthesis**
por: Healy, Alan R, et al.
Publicado: (2015)

Stereochemical Assignment of the Protein–Protein Interaction Inhibitor JBIR‐22 by Total Synthesis
por: Healy, Alan R., et al.
Publicado: (2015)

Stereochemical Assignment and Absolute Abundance of Nonproteinogenic Amino Acid Homoarginine in Marine Sponges
por: Mohanty, Ipsita, et al.
Publicado: (2021)

Synthesis and Vibrational Circular Dichroism Analysis of N-Heterocyclic Carbene Precursors Containing Remote Chirality Centers
por: Szabó, Zita, et al.
Publicado: (2022)

Stereochemical assignment, antiinflammatory properties, and receptor for the omega-3 lipid mediator resolvin E1
por: Arita, Makoto, et al.
Publicado: (2005)

Assignment of the CD Cotton Effect to the Chiral Center in Pseurotins, and the Stereochemical Revision of Pseurotin A(2)
por: Yamada, Takeshi, et al.
Publicado: (2016)

Stereochemical and Skeletal Diversity Arising from Amino Propargylic Alcohols
por: Pizzirani, Daniela, et al.
Publicado: (2010)

Glucopyranosylidene-Spiro-Thiazolinones: Synthetic Studies and Determination of Absolute Configuration by TDDFT-ECD Calculations
por: Szabó, Katalin E., et al.
Publicado: (2017)

Neuronal Modulators from the Coral-Associated Fungi Aspergillus candidus
por: Peng, Gao-Yang, et al.
Publicado: (2021)

Point-to-Axial Chirality Transmission: A Highly Sensitive Triaryl Chirality Probe for Stereochemical Assignments of Amines
por: Mądry, Tomasz, et al.
Publicado: (2020)

Peniciadametizine A, a Dithiodiketopiperazine with a Unique Spiro[furan-2,7'-pyrazino[1,2-b][1,2]oxazine] Skeleton, and a Related Analogue, Peniciadametizine B, from the Marine Sponge-Derived Fungus Penicillium adametzioides
por: Liu, Yang, et al.
Publicado: (2015)

Bioactive (3Z,5E)-11,20-Epoxybriara-3,5-dien-7,18-olide Diterpenoids from the South China Sea Gorgonian Dichotella gemmacea
por: Li, Cui, et al.
Publicado: (2011)

Stereochemical Study of the Super Large Tetrakis Alkaloid Alasmontamine A by Means of an Advanced Computational NMR
por: Semenov, Valentin A., et al.
Publicado: (2023)

An introduction to stereochemical restraints
por: Evans, Philip R.
Publicado: (2007)

Synthesis of the C1–C27 Fragment of Stambomycin D Validates Modular Polyketide Synthase-Based Stereochemical Assignments
por: Lim, Jieyan, et al.
Publicado: (2021)

Varioloid A, a new indolyl-6,10b-dihydro-5aH-[1]benzofuro[2,3-b]indole derivative from the marine alga-derived endophytic fungus Paecilomyces variotii EN-291
por: Zhang, Peng, et al.
Publicado: (2016)

Correction: Varioloid A, a new indolyl-6,10b-dihydro-5aH-[1]benzofuro[2,3-b]indole derivative from the marine alga-derived endophytic fungus Paecilomyces variotii EN-291
por: Zhang, Peng, et al.
Publicado: (2018)

Expanding Stereochemical and Skeletal Diversity Using Petasis Reactions and 1,3-Dipolar Cycloadditions
por: Muncipinto, Giovanni, et al.
Publicado: (2010)

Unambiguous Stereochemical Assignment of Cyclo(Phe-Pro), Cyclo(Leu-Pro), and Cyclo(Val-Pro) by Electronic Circular Dichroic Spectroscopy
por: Domzalski, Alison, et al.
Publicado: (2021)

Stereochemical studies on pheromonal communications
por: MORI, Kenji
Publicado: (2014)

In Vitro Biological Activity of Natural Products from the Endophytic Fungus Paraboeremia selaginellae against Toxoplasma gondii
por: Mazzone, Flaminia, et al.
Publicado: (2022)

Emergency logistics network optimization with time window assignment
por: Wang, Yong, et al.
Publicado: (2023)

Stereochemical Alignment in Triphospha[3]ferrocenophanes
por: Borucki, Stefan, et al.
Publicado: (2017)

The stereochemical course of 2-methylisoborneol biosynthesis
por: Gu, Binbin, et al.
Publicado: (2022)

Stereochemical and Biosynthetic Rationalisation of the Tropolone Sesquiterpenoids
por: Li, Lei, et al.
Publicado: (2022)

Natural-Product-Inspired Microwave-Assisted Synthesis of Novel Spirooxindoles as Antileishmanial Agents: Synthesis, Stereochemical Assignment, Bioevaluation, SAR, and Molecular Docking Studies
por: Sahu, Nawal Kishore, et al.
Publicado: (2023)

Expanding the chemical diversity of an endophytic fungus Bulgaria inquinans, an ascomycete associated with mistletoe, through an OSMAC approach
por: Ariantari, Ni P., et al.
Publicado: (2019)

A New Effective Algorithm for the Unambiguous Identification of the Stereochemical Characteristics of Compounds During Their Registration in Databases
por: Cieplak, T., et al.
Publicado: (2001)

Oxidized Juncuenin B Analogues with Increased Antiproliferative Activity on Human Adherent Cell Lines: Semisynthesis and Biological Evaluation
por: Bús, Csaba, et al.
Publicado: (2020)

Tautomerism troubles: proton transfer modifies the stereochemical assignments in diastereoisomeric structures of spirocyclic 5-methyl-2H-imidazol-4-amine dimers
por: Blade, Helen, et al.
Publicado: (2021)

Due-Window Assignment Scheduling with Variable Job Processing Times
por: Wu, Yu-Bin, et al.
Publicado: (2015)

Induction of New Lactam Derivatives From the Endophytic Fungus Aplosporella javeedii Through an OSMAC Approach
por: Gao, Ying, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_o3ut99e3g4538jlakf9qcj6shm