Facile Total Syntheses of Idarubicinone-7-β-D-glucuronide: Convenient Preparations of AB-Ring Synthon Using Some Carboxylic Acid Derivatives.

ChemInform ◽  
2004 ◽  
Vol 35 (39) ◽  
Author(s):  
Young S. Rho ◽  
Jihyung Park ◽  
Gyuil Kim ◽  
Hyesun Kim ◽  
Hongsig Sin ◽  
...  
Keyword(s):  
Carboxylic Acid ◽  
Total Syntheses ◽  
Ab Ring

Facile Total Syntheses of Idarubicinone‐7‐β‐D‐glucuronide: Convenient Preparations of AB‐Ring Synthon Using Some Carboxylic Acid Derivatives

2004 ◽  
Vol 34 (9) ◽  
pp. 1703-1722 ◽  
Author(s):  
Young S. Rho ◽  
Jihyung Park ◽  
Gyuil Kim ◽  
Hyesun Kim ◽  
Hongsig Sin ◽  
...  
Keyword(s):  
Carboxylic Acid ◽  
Total Syntheses ◽  
Ab Ring

Total syntheses and antiproliferative activities of prenostodione and its analogues

2021 ◽  
Author(s):  
Aldahir Ramos Orea ◽  
María Teresa Ramírez-Apan ◽  
Rosa M. Chávez-Santos ◽  
Rodrigo Aguayo-Ortiz ◽  
Clara I Espitia ◽  
...  
Keyword(s):  
Carboxylic Acid ◽  
Total Synthesis ◽  
Indole Alkaloid ◽  
Total Syntheses ◽  
Antiproliferative Activities

A high-yielding total synthesis of the indole alkaloid prenostodione was completed in 4 steps and 44% overall yield from 1H-indole-3-carboxylic acid. The expedient syntheses of prenostodiones containing distinct substituents at...

scholarly journals Studi Sintesis Analog Piokelin III: Sintesis Asam 3-Asetil-2-(2-(2-Hidroksifenil)- 4,5-Dihidrotiazol-4-Il)Tiazolidine-4-Karboksilat

2018 ◽  
Vol 10 (1) ◽  
pp. 49
Author(s):  
Adel Zamri
Keyword(s):  
Carboxylic Acid ◽  
Acetic Anhydride ◽  
Total Syntheses

The total syntheses of 3-acetyl-2-(2-(2-hydroxyphenyl)-4,5-dihydrothiazole-4-yl) thiazolidine-4-carboxylic acid, a new pyochelin analog is described. The molecule intermediate 4’-(2-hydroxy-phenyl)-2,3,4,5,2’,5,-hexahydro- [2,2’]bithiazolil-4-carboxylic acid was obtained in 4 steps reaction from 2-hydroxybenzonitrile in good yields. The Nacetylation of molecule intermediate was carried out by acetic anhydride to produce pyochelin analog in moderate yields.

Procedure-Economical, Enantioselective Total Syntheses of Polycyclic Natural Products and Analogues Containing a 3a-Hydroxyhexahydropyrrolo[2,3-b]indole-2-carboxylic Acid Residue

Synlett ◽  
2020 ◽  
Vol 31 (17) ◽  
pp. 1681-1690
Author(s):  
Pei-Qiang Huang
Keyword(s):  
Natural Products ◽  
Carboxylic Acid ◽  
Tandem Reactions ◽  
Protecting Group ◽  
Future Perspectives ◽  
Total Syntheses ◽  
Bioactive Natural Products ◽  
Regioselective Reactions ◽  
Enantioselective Syntheses

The 3a-hydroxyhexahydropyrrolo[2,3-b]indole-2-carboxylic acid (HPIC) residue and its aza-analogue are found in many bioactive natural products. In this account, short divergent total syntheses of several such natural products, diastereomers and analogues are described. It is demonstrated that by appropriate combination of different efficient tactics such as biomimetic/bio-inspired synthesis, chemo/regioselective reactions, umpolung of regioselectivity and/or reactivity, and tandem reactions, the enantioselective syntheses of polycyclic molecules such as (+)-asperlicin E and (–)-robustanoids A and B can be achieved in a protecting-group-free and redox-economical manner, in only three to four steps starting from l-tryptophan.1 Introduction2 Strategic Considerations2.1 Occurrence of HO-HPIC and HO-aza-HPIC Residues in Natural Products2.2 Biosyntheses of HO-HPIC and HO-aza-HPIC Residues2.3 Chemical Syntheses of HO-HPIC and HO-aza-HPIC Residues3 Procedure-Economical Syntheses of HO-HPIC-Containing Natural Products3.1 Protecting-Group-Free Syntheses of Asperlicin E, Its Diastereomer, and an Analogue3.2 Divergent Syntheses of (–)-Robustanoids A and B, a Diastereomer, and Analogues4 Conclusion and Future Perspectives

Extension of the Modified Julia Olefination on Carboxylic Acid Derivatives: Scope and Applications

Synlett ◽  
2017 ◽  
Vol 29 (01) ◽  
pp. 34-45 ◽  
Author(s):  
David Gueyrard
Keyword(s):  
Carboxylic Acid ◽  
Total Synthesis ◽  
Enol Ether ◽  
Enol Ethers ◽  
Total Syntheses ◽  
Bistramide A ◽  
Enol Esters ◽  
Jaspine B ◽  
Ether Synthesis ◽  
Julia Olefination

This account relates our work in the field of modified Julia olefination to extend this very useful olefination method to carboxylic acid derivatives. Since our preliminary results on lactones in 2005, the reaction has been extended to a large range of derivatives (lactams, imides and anhydrides) through an intra- or intermolecular process leading to a great variety of structures (enol ethers, enamides and exo enol esters). This article will also focus on the application of this methodology for the preparation of biologically interesting compounds and/or total syntheses of natural products such as C-disaccharide, bistramide A, jaspine B and maculalactone B.1 Introduction2 Modified Julia Olefination on Lactones2.1 Methylene Enol Ether Synthesis2.2 Substituted Enol Ether Synthesis2.3 Monofluorinated Enol Ether Synthesis2.4 Difluorinated Enol Ether Synthesis3 Applications3.1 Spiroketal Synthesis3.2 Spirocompound Synthesis3.3 Pseudodisaccharide Synthesis3.4 Total Synthesis of Jaspine B4 Modified Julia Olefination on Other Carboxylic Acid Derivatives4.1 Lactam Olefination and Spiroaminal Synthesis4.2 Bicyclic Enamide Synthesis by Intramolecular Modified Julia Olefination on Imides4.3 Modified Julia Olefination on Anhydrides5 Conclusion

Fibrinolytic Activity of Cerebro-Spinal Fluid and the Development of Artificial Cerebral Haematomas in Dogs

1969 ◽  
Vol 21 (02) ◽  
pp. 294-303 ◽  
Author(s):  
H Mihara ◽  
T Fujii ◽  
S Okamoto
Keyword(s):  
Cerebrospinal Fluid ◽  
Carboxylic Acid ◽  
Fibrinolytic Activity ◽  
Clinical Implications ◽  
Trans Form ◽  
Plate Method ◽  
Blood Samples ◽  
Fibrin Plate ◽  
The Brain

SummaryBlood was injected into the brains of dogs to produce artificial haematomas, and paraffin injected to produce intracerebral paraffin masses. Cerebrospinal fluid (CSF) and peripheral blood samples were withdrawn at regular intervals and their fibrinolytic activities estimated by the fibrin plate method. Trans-form aminomethylcyclohexane-carboxylic acid (t-AMCHA) was administered to some individuals. Genera] relationships were found between changes in CSF fibrinolytic activity, area of tissue damage and survival time. t-AMCHA was clearly beneficial to those animals given a programme of administration. Tissue activator was extracted from the brain tissue after death or sacrifice for haematoma examination. The possible role of tissue activator in relation to haematoma development, and clinical implications of the results, are discussed.

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