z-logo
Premium
Diastereoselective Synthesis of Z‐Alkenyl Disulfides from α‐Thiophosphorylated Ketones and Thiosulfonates
Author(s) -
Musiejuk Mateusz,
Doroszuk Justyna,
Jędrzejewski Bartosz,
Ortiz Nieto Gregory,
Marin Navarro Marisol,
Witt Dariusz
Publication year - 2020
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201901208
Subject(s) - chemistry , base (topology) , combinatorial chemistry , reaction conditions , bearing (navigation) , organic chemistry , stereochemistry , polymer chemistry , catalysis , mathematical analysis , mathematics , cartography , geography
We developed a simple and efficient method for the synthesis of functionalized unsymmetrical Z ‐alkenyl disulfides under mild conditions in moderate to good yields. The designed method is based on the reaction of α‐thiophosphorylated carbonyl compounds with thiotosylates in the presence of a base. The developed method allows the preparation of unsymmetrical Z ‐alkenyl disulfides bearing additional hydroxy, carboxy, or ester functionalities

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom