scholarly journals IL PROFUMO DI PULITO

2012 ◽  
Author(s):  
Claudio Fuganti ◽  
Maria Elisabetta Brenna
Keyword(s):  
Organic Chemistry ◽  
Total Synthesis ◽  
Aromatic Compounds ◽  
Natural Sources ◽  
Synthetic Organic Chemistry ◽  
Odorous Substances

Modern perfumery was born nearly a century ago, when synthetic organic chemistry made available a great variety of products, besides those traditionally obtained by extraction from nature: pure or enriched compounds isolated from natural sources, semi-synthetic products prepared from natural starting materials, aromatic compounds obtained by total synthesis. The most relevant results achieved in the last decade are herein presented for several types of odorous substances.

scholarly journals Recent Chemical Methodology Advances in the Total Synthesis of Meroterpenoids

2021 ◽  
Vol 68 (2) ◽  
pp. 247-267
Author(s):  
Jan Petrovčič ◽  
Chad Nicholas Ungarean ◽  
David Sarlah
Keyword(s):  
Organic Chemistry ◽  
Natural Products ◽  
Total Synthesis ◽  
Feature Article ◽  
Total Syntheses ◽  
Synthetic Organic Chemistry ◽  
Synthetic Studies

Heterogeneity of meroterpenoids arising from their dual biosynthetic origins is constantly provoking synthetic chemists to utilize their ingenuity and revise their retrosynthetic logic. By studying recent publications on meroterpenoid synthesis,tremendous advances in the field of synthetic organic chemistry can be witnessed. This feature article covers some of the most intriguing total syntheses and synthetic studies towards the meroterpenoid class of natural products from the last five years.

Strategies for the synthesis of furo-pyranones and their application in the total synthesis of related natural products

2021 ◽  
Author(s):  
Sagar Sudam Thorat ◽  
Ravindar Kontham
Keyword(s):  
Organic Chemistry ◽  
Molecular Structure ◽  
Natural Products ◽  
Total Synthesis ◽  
Small Molecules ◽  
Synthetic Organic Chemistry

The furo-pyranone framework is widely present in the molecular structure of various biologically potent natural products and un-natural small molecules, and it represents a valuable target in synthetic organic chemistry...

scholarly journals Recent developments in photoredox-catalyzed remote ortho and para C–H bond functionalizations

2020 ◽  
Vol 16 ◽  
pp. 248-280 ◽  
Author(s):  
Rafia Siddiqui ◽  
Rashid Ali
Keyword(s):  
Organic Chemistry ◽  
Total Synthesis ◽  
Research Area ◽  
Photoredox Catalysis ◽  
Organic Transformations ◽  
Research Papers ◽  
Bond Functionalization ◽  
Synthetic Organic Chemistry ◽  
Recent Developments ◽  
The Impact

In recent years, the research area of direct C–H bond functionalizations was growing exponentially not only due to the ubiquity of inert C–H bonds in diverse organic compounds, including bioactive natural and nonnatural products, but also due to its impact on the discovery of pharmaceutical candidates and the total synthesis of intricate natural products. On the other hand, more recently, the field of photoredox catalysis has become an indispensable and unparalleled research topic in modern synthetic organic chemistry for the constructions of challenging bonds, having the foremost scope in academia, pharmacy, and industry. Therefore, the development of green, simpler, and effective methodologies to accomplish direct C–H bond functionalization is well overdue and highly desirable to the scientific community. In this review, we mainly highlight the impact on, and the utility of, photoredox catalysts in inert ortho and para C–H bond functionalizations. Although a surge of research papers, including reviews, demonstrating C–H functionalizations have been published in this vital area of research, to our best knowledge, this is the first review that focuses on ortho and para C–H functionalizations by photoredox catalysis to provide atom- and step-economic organic transformations. We are certain that this review will act as a promoter to highlight the application of photoredox catalysts for the functionalization of inert bonds in the domain of synthetic organic chemistry.

Recent Developments in the Asymmetric Detrifluoroacetylative Reactions of in situ Generated Mono-Fluorinated Enolates

2020 ◽  
Vol 24 (18) ◽  
pp. 2181-2191
Author(s):  
Li Wang ◽  
Ziyi Li ◽  
Jiang Liu ◽  
Jianlin Han ◽  
Hiroki Moriwaki ◽  
...  
Keyword(s):  
Organic Chemistry ◽  
Bond Cleavage ◽  
Synthetic Methodology ◽  
Research Topics ◽  
Synthetic Organic Chemistry ◽  
Nucleophilic Reactions ◽  
F Center ◽  
Recent Developments

The development of an efficient and mild synthetic methodology for the construction of bioactive fluorine-containing molecules represents one of the hot research topics in general synthetic organic chemistry. In this review, some recent progresses achieved in the development of detrifluoroacetylatively generated mono-fluorinated enolates via CC bond cleavage and their asymmetric nucleophilic reactions for assembly of chiral quaternary C-F center containing compounds.

An approach to computer-assisted drill in synthetic organic chemistry

1973 ◽  
Vol 50 (9) ◽  
pp. 645
Author(s):  
H. A. Clark ◽  
J. C. Marshall ◽  
T. L. Isenhour
Keyword(s):  
Organic Chemistry ◽  
Computer Assisted ◽  
Synthetic Organic Chemistry

Recent advances and perspectives in manganese-catalyzed C–H activation

2021 ◽  
Author(s):  
Thaipparambil Aneeja ◽  
Mohan Neetha ◽  
C. M. A. Afsina ◽  
Gopinathan Anilkumar
Keyword(s):  
Organic Chemistry ◽  
Synthetic Organic Chemistry ◽  
Recent Advances

Manganese-catalyzed C–H activation has become an emerging area in organic chemistry. These efficient and eco-friendly manganese catalysed reactions provides new opportunities in the field of synthetic organic chemistry.

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