2015
DOI: 10.1055/s-0035-1560378
|View full text |Cite
|
Sign up to set email alerts
|

Cobalt-Catalysed Bond Formation Reactions; Part 2

Abstract: This review summarises the cobalt-catalysed reactions of the years 2008 through 2014. Covered are addition reactions, such as the hydrogenation of double bonds, the addition of C-H bonds to double and triple bonds, C-H activation reactions, cobalt-catalysed cross-coupling reactions and selected additions of H-B and H-Si bonds to unsaturated starting materials. The cobalt-catalysed cycloadditions range from cyclopropanations, [2+2], Pauson-Khand reactions, [2+2+2], [4+2], [6+2] cycloadditions as well as benzann… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 33 publications
(2 citation statements)
references
References 282 publications
(298 reference statements)
0
2
0
Order By: Relevance
“…Electrophile-promoted cyclization , and CuAAC of 1-iodoacetylenes , being applied to diacetylenes , with subsequent Sonogashira coupling , have been suggested as key steps for the construction of acyclic enediyne systems. The Nicholas reaction was chosen for the final macrocyclization step as a unique synthetic tool for the construction of various cyclic alkyne derivatives including natural enediynes and their analogues. …”
Section: Resultsmentioning
confidence: 99%
“…Electrophile-promoted cyclization , and CuAAC of 1-iodoacetylenes , being applied to diacetylenes , with subsequent Sonogashira coupling , have been suggested as key steps for the construction of acyclic enediyne systems. The Nicholas reaction was chosen for the final macrocyclization step as a unique synthetic tool for the construction of various cyclic alkyne derivatives including natural enediynes and their analogues. …”
Section: Resultsmentioning
confidence: 99%
“…Over the last decade the application of the cobalt catalytic system CoBr 2 /phosphine ligand/Zn/ZnI 2 for the carbon–carbon bond formation has become a subject of a growing interest (for reviews see [1521]). This catalytic system has many advantages, including the availability of the cobalt salts and high tolerance to organic functional groups (for some recent examples see [2227]).…”
Section: Introductionmentioning
confidence: 99%