Search engine for discovering works of Art, research articles, and books related to Art and Culture
Javascript must be enabled to continue!
ChemInform Abstract: Asymmetric Epoxidation of Allylic Alcohols: The Katsuki‐Sharpless Epoxidation Reaction
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: Asymmetric Epoxidation of Allylic Alcohols: The Katsuki‐Sharpless Epoxidation Reaction
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
Asymmetric Epoxidation of Allylic Alcohols: the Katsuki–Sharpless Epoxidation Reaction
Asymmetric Epoxidation of Allylic Alcohols: the Katsuki–Sharpless Epoxidation Reaction
AbstractIn 1980, Sharpless and Katsuki discovered a system for the asymmetric epoxidation of primary allylic alcohols that utilizes Ti(OPr‐i)4, a dialkyl tartrate as a chiral ligan...
Isolation, characterization and semi-synthesis of natural products dimeric amide alkaloids
Isolation, characterization and semi-synthesis of natural products dimeric amide alkaloids
Isolation, characterization of natural products dimeric amide alkaloids from roots of the Piper chaba Hunter. The synthesis of these products using intermolecular [4+2] cycloaddit...
Jacobsen‐Katsuki Epoxidation
Jacobsen‐Katsuki Epoxidation
AbstractThe Jacobsen and Katsuki have reported the improvement of olefin epoxidation, using a sophisticated chiral salen ligand for manganese complexes, which resulted in high enan...
Sharpless Asymmetric Dihydroxylation: An Impressive Gadget for the Synthesis of Natural Products: A Review
Sharpless Asymmetric Dihydroxylation: An Impressive Gadget for the Synthesis of Natural Products: A Review
Sharpless asymmetric dihydroxylation is an important reaction in the enantioselective synthesis of chiral vicinal diols that involves the treatment of alkene with osmium tetroxide ...
Developmental Toxicology of Industrial Alcohols: A Summary of 13 Alcohols Administered by Inhalation to Rats
Developmental Toxicology of Industrial Alcohols: A Summary of 13 Alcohols Administered by Inhalation to Rats
The developmental toxicology of 13 industrial alcohols (methanol, ethanol, 1-propanol, isopropanol, 1-butanol, 2-butanol, tertiary-butanol, 1-pentanol, 1-hexanol, 2-ethyl-1-hexanol...
Comparisons of metal oxides activity in the transesterification of triglycerides by С1–С4 alcohols
Comparisons of metal oxides activity in the transesterification of triglycerides by С1–С4 alcohols
The activity of heterogeneous catalysts for the transesterification reaction of sunflower oil triglycerides with aliphatic alcohols of normal structure was investigated in this wor...
Active, selective, and stable single-component precatalysts for asymmetric allylic alkylation
Active, selective, and stable single-component precatalysts for asymmetric allylic alkylation
The stereoselective construction of new carbon-element bonds is a crucial aspect of organic synthesis. Among the many strategies developed to date, palladium-catalysed asymmetric a...
Plasticizing Effectiveness and Characteristics of Different Mono‐Alcohols, Di‐Alcohols, and Polyols for Starch‐Based Materials
Plasticizing Effectiveness and Characteristics of Different Mono‐Alcohols, Di‐Alcohols, and Polyols for Starch‐Based Materials
AbstractThe effectiveness of various alcohols as plasticizers for starch‐based materials is studied. Specifically, the impact of molecular structures, such as the number of hydroxy...