Dimethylsulfoxonium Methylide

Ng, John S.; Liu, Chin; Aggarwal, Varinder K.; Winn, C. L.

doi:10.1002/047084289x.rd385.pub2

Search citation statements

Order By: Relevance

Paper Sections

Select...

Methyl Iodide (Mei) and Its Derivatives1

Citation Types

Supporting

Mentioning

Contrasting

Year Published

2018

Publication Types

Select...

Article1

Relationship

Self Cite0

Independent1

Authors

Journals

Cited by 1 publication

(1 citation statement)

References 108 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Besides epoxidation, DIMSOYh as been used for methylation. [160] Recently,G anguly, Chakraborty,a nd co-workersr eported the C-methylation att he 2-position of 2-carboxy-4-chromanones by using freshly prepared DIMSOY. [161] The reactionw as performed through av ery mild and simple approach:f irst, DIMSOY was prepared from TMSO-I in DMSO with cooling in an ice bath;s econd, to the DIMSOY solution was added chromone-2-carboxylates.…”

Section: Methyl Iodide (Mei) and Its Derivativesmentioning

confidence: 99%

Recent Advances in Methylation: A Guide for Selecting Methylation Reagents

Chen

2018

Chemistry A European J

199

121

View full text Add to dashboard Cite

Methylation is a well‐known structural modification in organic and medicinal chemistry. This review summarizes recent advances in methylation by categorizing specific methylation reagents. The challenges of mono N‐methylation of aliphatic amines and N‐methylation of peptides are discussed. This review will be useful for chemists wanting to select the appropriate reagents for methylation chemistry. Based on the large diversity of methylation reagents and their wide scope, this review also broadens perspectives on which strategies to select for utilizing a particular methylation, resulting in an increased flexibility in synthetic route planning.

show abstract

Section: Methyl Iodide (Mei) and Its Derivativesmentioning

confidence: 99%