C−C, C−S, and C−N Coupling versus Dealkylation Processes in the Cationic Tris(thiolato)dimolybdenum(III) Complexes [Mo2Cp2(μ-SMe)3L2]+ (L = xylNC, t-BuNC, CO, MeCN)-Reference-Cited by-同舟云学术

C−C, C−S, and C−N Coupling versus Dealkylation Processes in the Cationic Tris(thiolato)dimolybdenum(III) Complexes [Mo2Cp2(μ-SMe)3L2]+ (L = xylNC, t-BuNC, CO, MeCN)

Published:2008-07-30 Issue:16 Volume:27 Page:4207-4222
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Ojo Wilfried-Solo¹,Pétillon François Y.¹,Schollhammer P.¹,Talarmin Jean¹

Affiliation:

1. UMR CNRS 6521, Chimie, Electrochimie Moléculaires et Chimie Analytique, UFR Sciences et Techniques, Université de Bretagne Occidentale, CS 93837, 29238 Brest-Cedex 3, France

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om8003702

Reference114 articles.

1. Activation of a CNXylyl ancillary ligand in the reaction of electron-deficient alkynes with a phosphido niobocene complex

2. Ligand exchange reactions within the coordination sphere of a molybdenum η2(4e)-alkyne complex: the formation of an indole in a cascade reaction involving an alkyne and isonitrile ligands

3. Reactions of Isocyanide-Substituted Dimanganese Carbonyl Complexes with Alkynes. Alkyne-Isocyanide Coupling and the Synthesis of Metalated N-Substituted Pyridines

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