Results 181 to 190 of about 938,190 (242)
Transition Metal-Free Borata-Alkene/Alkyne Metathesis Enables Access to Cyclopentenes. [PDF]
Dong W +8 more
europepmc +1 more source
C─S Bond Metathesis Reactions: Concepts, Scope, and Mechanistic Insight. [PDF]
Liu H, Xie Y.
europepmc +1 more source
Divergent and programmable skeletal remodeling of complex macrocycles with a small method set. [PDF]
Nikbakht A +4 more
europepmc +1 more source
Olefin Metathesis Catalyzed by a Latent Ruthenathiete Complex. [PDF]
Pabarue AB +4 more
europepmc +1 more source
Direct metathesis deconstruction to recycle poly(dicyclopentadiene) composites. [PDF]
Mason KS +18 more
europepmc +1 more source
Ring-Closing Metathesis in Carbohydrate Annulation
Even eight-membered rings (such as in 2) can be formed by ring-closing metathesis of glucose derivatives such as 1. Enantiomerically pure tricyclic spiro compounds can also be prepared.
Holt, DJ +7 more
openaire +3 more sources
Ring-Closing Metathesis Approach to Dictyostatin
[reaction: see text] An esterification/ring-closing metathesis approach to dictyostatin and discodermolide is introduced. The approach provides for facile fragment coupling of two main segments of these natural products at the C10-C11 alkene with high to complete Z-selectivity.
Cyrous O, Kangani +2 more
openaire +3 more sources
Solvents for ring-closing metathesis reactions
A study of the influence of eight diverse solvents on a Grubbs II-catalysed ring-closing metathesis (RCM) reaction reveals a complex dependence of the different reaction steps on the solvent and suggests acetic acid as a useful solvent for RCM reactions.
Claire S, Adjiman +3 more
openaire +3 more sources
AbstractRing-closing metathesis (RCM) has emerged as a powerful synthetic tool. Depending on the unsaturated functional groups involved, ring-closing-metathesis reactions are classified into three categories: diene ring-closing metathesis, enyne ring-closing metathesis, and diyne ring-closing metathesis.
D. Lee, V. R. Sabbasani
openaire +2 more sources

