Base Metal‐Catalyzed C‐Methylation Reactions Using Methanol. Issue 22 (6th October 2021)
- Record Type:
- Journal Article
- Title:
- Base Metal‐Catalyzed C‐Methylation Reactions Using Methanol. Issue 22 (6th October 2021)
- Main Title:
- Base Metal‐Catalyzed C‐Methylation Reactions Using Methanol
- Authors:
- Sarki, Naina
Goyal, Vishakha
Natte, Kishore
Jagadeesh, Rajenahally V. - Abstract:
- Abstract: C‐methylation is a vitally important reaction applicable in chemical synthesis and structure‐based drug design. Notably, the "magic methyl" effect has become decisive in medicinal chemistry and drug discovery for the modulation of bio‐active properties in life science molecules. In this regard, C‐methylation reaction is widely applied chemical modification in various biomolecules, pharmaceuticals, and natural products. In general, this reaction often relies on activated, hazardous and uneconomical methyl sources such as diazomethane, dimethyl sulfate, and methyl halides. To achieve methylation reactions in a sustainable and cost‐effective manner, the use of 'ideal' C1 source is crucial. In this regard, methanol constitutes an expedient −CH3 source because this simple alcohol is less‐hazardous, inexpensive, and abundantly available platform chemical as well as it produces only water as the by‐product in methylation processes. Regarding potential catalysts to perform C‐methylation using methanol by hydrogen borrowing methodology, non‐noble metal‐based catalysts are highly preferable due to their unique advantages such as more abundance, inexpensive and low‐toxicity. In recent years, chemists made significant contributions towards catalytic valorization of methanol as C1 source to insert methyl groups via C−H activation in a variety of compounds and life science molecules. Consequently, in this minireview we summarize the C‐methylation process using methanol byAbstract: C‐methylation is a vitally important reaction applicable in chemical synthesis and structure‐based drug design. Notably, the "magic methyl" effect has become decisive in medicinal chemistry and drug discovery for the modulation of bio‐active properties in life science molecules. In this regard, C‐methylation reaction is widely applied chemical modification in various biomolecules, pharmaceuticals, and natural products. In general, this reaction often relies on activated, hazardous and uneconomical methyl sources such as diazomethane, dimethyl sulfate, and methyl halides. To achieve methylation reactions in a sustainable and cost‐effective manner, the use of 'ideal' C1 source is crucial. In this regard, methanol constitutes an expedient −CH3 source because this simple alcohol is less‐hazardous, inexpensive, and abundantly available platform chemical as well as it produces only water as the by‐product in methylation processes. Regarding potential catalysts to perform C‐methylation using methanol by hydrogen borrowing methodology, non‐noble metal‐based catalysts are highly preferable due to their unique advantages such as more abundance, inexpensive and low‐toxicity. In recent years, chemists made significant contributions towards catalytic valorization of methanol as C1 source to insert methyl groups via C−H activation in a variety of compounds and life science molecules. Consequently, in this minireview we summarize the C‐methylation process using methanol by applying Fe‐, Mn‐, Co‐ and Ni‐based catalysts as well as metal free catalysts. Abstract : … (more)
- Is Part Of:
- Advanced synthesis & catalysis. Volume 363:Issue 22(2021)
- Journal:
- Advanced synthesis & catalysis
- Issue:
- Volume 363:Issue 22(2021)
- Issue Display:
- Volume 363, Issue 22 (2021)
- Year:
- 2021
- Volume:
- 363
- Issue:
- 22
- Issue Sort Value:
- 2021-0363-0022-0000
- Page Start:
- 5028
- Page End:
- 5046
- Publication Date:
- 2021-10-06
- Subjects:
- C-Methylation -- Methanol -- Base metal catalysts -- Borrowing hydrogen technology
Catalysis -- Periodicals
Organic compounds -- Synthesis -- Periodicals
Chemistry -- Periodicals
Chemistry, Technical -- Periodicals
Chemistry -- Periodicals
Catalysis -- Periodicals
Technology, Pharmaceutical -- Periodicals
547.2 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1615-4169 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adsc.202100762 ↗
- Languages:
- English
- ISSNs:
- 1615-4150
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.931980
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20022.xml