57187-83-4Relevant academic research and scientific papers
Visible-Light-Mediated Three-Component Radical Iodosulfonylative Cyclization of Enynes
Cheng, Qi,Zhang, Fengrong,Chen, Xiaoyun,Han, Ying,Yan, Chaoguo,Shi, Yaocheng,Hou, Hong,Zhu, Shaoqun
, p. 2515 - 2519 (2022/04/14)
An efficient three-component radical iodosulfonylative cyclization of enynes is described. The visible-light irradiation of iodoform with sulfinates enables sulfonyl radical generation under catalyst- and oxidant-free conditions and triggers the radical a
Oxygen-Tethered 1,6-Enynes and [41.0]-Bicyclic Ether Skeletons as Hedonic Materials for the Fragrance Industry
Laher, Romain,Gentilini, Emilie,Marin, Christophe,Michelet, Véronique
, p. 4020 - 4029 (2021/08/10)
The synthesis of original structures for the fragrance industry bearing bicyclic scaffolds is described. To the best of our knowledge, these structures are not found in the fragrance industry, neither from natural nor synthetic pathways. NHC-gold-type catalysts showed excellent activities leading to light bicyclic enol ethers. Several bicyclic adducts were prepared in good to excellent yields (18-99%). Evaluation of NHC-Au complexes allowed to reach a TOF of 300 h -1. The evaluation for the organoleptic properties of [4.1.0]-bicyclic ethers were compared with the unprecedented properties of the 1,6-enyne precursors. Evaluations of starting materials showed a great interest in these structures with various olfactory facets. In this study, we depicted the similarity and differences between starting ethers and their cycloisomerized bicyclic counterparts.
When Gold Meets Perfumes: Synthesis of Olfactive Compounds via Gold-Catalyzed Cycloisomerization Reactions
Laher, Romain,Marin, Christophe,Michelet, Véronique
supporting information, p. 4058 - 4062 (2020/04/20)
An efficient, and mild synthetic route for the preparation of functionalized volatile oxa-bicyclo[4.1.0]-hept-4-ene (29 compounds, 44-98% isolated yields) has been developed relying on the association of IPrAuCl with NaBArF. The remarkable selectivity was demonstrated on a 1 g and 25 g scale with low catalyst loadings. The synthetic utility of these low-molecular-weight enols was further demonstrated by the derivatization of some adducts and by the unprecedented olfactory evaluation of all bicyclic derivatives.
Gold(I)-catalyzed intramolecular [4+2] cycloadditions of arylalkynes or 1,3-enynes with alkenes: Scope and mechanism
Nieto-Oberhuber, Cristina,Perez-Galan, Patricia,Herrero-Gomez, Elena,Lauterbach, Thorsten,Rodriguez, Cristina,Lopez, Salome,Bour, Christophe,Rosellon, Antonio,Cardenas, Diego J.,Echavarren, Antonio M.
, p. 269 - 279 (2008/09/20)
The cyclizations of enynes substituted at the alkyne gives products of formal [4+2] cyclization with Au(I) catalysts. 1,8-Dien-3-ynes cyclize by a 5-exo-dig pathway to form hydrindanes. 1,6-Enynes with an aryl ring at the alkyne give 2,3,9,9a-tetrahydro-1
