Use of allylzinc halide as a source of halide: Differential addition of nucleophiles to Ts-aziridines and aldehydes under similar reaction conditions › Research Explorer

Use of allylzinc halide as a source of halide: Differential addition of nucleophiles to Ts-aziridines and aldehydes under similar reaction conditions

Research output: Contribution to journal › Article › peer-review

DOI

https://doi.org/10.1016/j.tetlet.2018.12.027
Final published version

Rana Chatterjee
Satyajit Samanta
Anindita Mukherjee
Sougata Santra
Grigory V. Zyryanov
Adinath Majee

Original language	English
Pages (from-to)	276-283
Number of pages	8
Journal	Tetrahedron Letters
Volume	60
Issue number	3
DOIs	https://doi.org/10.1016/j.tetlet.2018.12.027
Publication status	Published - 17 Jan 2019

WoS ResearchAreas Categories

Chemistry, Organic

Research areas

Allylation, Allylic halides, Aziridine, Carbonyls, Halogenations, PROMOTED ALLYLATION, BOND-FORMING REACTIONS, HOMOALLYLIC ALCOHOLS, N-TOSYLAZIRIDINES, IONIC LIQUID, SALT, EPOXIDES, RING, CARBONYL ADDITION, INDIUM

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

ID: 8540342