Mo-Based Complexes with Two Aryloxides and a Pentafluoroimido Ligand: Catalysts for Efficient Z-Selective Synthesis of a Macrocyclic Trisubstituted Alkene by Ring-Closing Metathesis
Olefin metathesis catalysts for controlling the formation of trisubstituted macrocyclic Z alkenes have been developed. The most effective complexes are Mo alkylidenes with a pentafluorophenylimido group and two large aryloxide ligands. The macrocyclic lactone precursor to anticancer agents epothilon...
Main Authors: | Wang, Chenbo, Haeffner, Fredrik, Hoveyda, Amir H., Schrock, Richard Royce |
---|---|
Other Authors: | Massachusetts Institute of Technology. Department of Chemistry |
Format: | Article |
Language: | en_US |
Published: |
Wiley Blackwell
2014
|
Online Access: | http://hdl.handle.net/1721.1/86095 https://orcid.org/0000-0001-5827-3552 |
Similar Items
-
Synthesis of E- and Z-trisubstituted alkenes by catalytic cross-metathesis
by: Nguyen, Thach T., et al.
Published: (2018) -
Efficient and Selective Formation of Macrocyclic Disubstituted Z Alkenes by Ring-Closing Metathesis (RCM) Reactions Catalyzed by Mo- or W-Based Monoaryloxide Pyrrolide (MAP) Complexes: Applications to Total Syntheses of Epilachnene, Yuzu Lactone, Ambrettolide, Epothilone C, and Nakadomarin A
by: Wang, Chenbo, et al.
Published: (2014) -
Kinetically E-selective macrocyclic ring-closing metathesis
by: Shen, Xiao, et al.
Published: (2018) -
Z-Selective and Syndioselective Ring-Opening Metathesis Polymerization (ROMP) Initiated by MonoAryloxidePyrrolide (MAP) Catalysts
by: Flook, Margaret M., et al.
Published: (2012) -
Highly Z- and Enantioselective Ring-Opening/Cross-Metathesis Reactions Catalyzed by Stereogenic-at-Mo Adamantylimido Complexes
by: Ibrahem, Ismail, et al.
Published: (2013)