Javascript must be enabled to continue!
ChemInform Abstract: Stereoselective Synthesis of C‐Glycosides via Tebbe Methylenation and Claisen Rearrangement.
View through CrossRef
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Title: ChemInform Abstract: Stereoselective Synthesis of C‐Glycosides via Tebbe Methylenation and Claisen Rearrangement.
Description:
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals.
To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option.
The original article is trackable via the “References” option.
Related Results
Lombardo Methylenation
Lombardo Methylenation
AbstractThe modification of the Takai–Nozaki methylenation (also known as the Nozaki–Hayashe methylenation) to convert ketones/aldehydes into alkenes using the “low temperature age...
Tebbe Olefination
Tebbe Olefination
Abstract
The transformation of a carbonyl group into a terminal vinyl group by means of low‐valent titanium alkylidene complexes, especially a methylene comp...
A Review on Chemical Structure and Biological Activities of Monoterpene Glycosides
A Review on Chemical Structure and Biological Activities of Monoterpene Glycosides
Abstract:
Monoterpene glycosides are important active ingredients in many commonly used traditional Chinese
medicines. Based on their different aglycones, monoterpene glycosides ar...
Synthesis of α‐C‐Glycosides via Tandem Tebbe Methylenation and Claisen Rearrangement.
Synthesis of α‐C‐Glycosides via Tandem Tebbe Methylenation and Claisen Rearrangement.
AbstractFor Abstract see ChemInform Abstract in Full Text....
Synthetic Studies towards Fungal glycosides: An Overview
Synthetic Studies towards Fungal glycosides: An Overview
Fungi have provided intriguing chemical diversity and have additionally proven to
be a tremendous source for a great variety of therapeutic molecules. Various fungal glycosides
hav...
The enantioselective Organocatalytic [1,2]-Rearrangement of Allylic Ammonium Ylides
The enantioselective Organocatalytic [1,2]-Rearrangement of Allylic Ammonium Ylides
The [1,2]-rearrangement of allylic ammonium ylides is traditionally observed as a competitive minor pathway alongside the thermally allowed [2,3]-sigmatropic rearrangement. The cha...
The Enantioselective Organocatalytic [1,2]-Rearrangement of Allylic Ammonium Ylides
The Enantioselective Organocatalytic [1,2]-Rearrangement of Allylic Ammonium Ylides
The [1,2]-rearrangement of allylic ammonium ylides is traditionally observed as a competitive minor pathway alongside the thermally allowed [2,3]-sigmatropic rearrangement. The cha...
Immunochromatographic assay for the detection of pseudojujubogenin glycosides
Immunochromatographic assay for the detection of pseudojujubogenin glycosides
AbstractIntroductionBacopa monnieri contains pseudojujubogenin glycosides as pharmacologically active compounds. In order to screen large numbers of plant samples for the presence ...

