Catalytic tin radical mediated tricyclisations. Part 2 †‡

Kelly, David R.; Picton, Mark R.

doi:10.1039/b000662i

Search citation statements

Order By: Relevance

Paper Sections

Select...

Oxygen Heterocycles1

Citation Types

Supporting

Mentioning

Contrasting

Year Published

2000

2019

Publication Types

Select...

Article3

Other2

Book1

Relationship

Self Cite0

Independent6

Authors

Journals

Cited by 7 publications

(1 citation statement)

References 28 publications

(18 reference statements)

Supporting

Mentioning

Contrasting

Order By: Relevance

“…A novel protocol uses a cascade reaction in which three rings are constructed in a single reaction and an example is illustrated in Scheme 26. 109…”

Section: Oxygen Heterocyclesmentioning

confidence: 99%

Synthesis of heterocycles by radical cyclisation

Bowman

Cloonan

Krintel

2001

J. Chem. Soc., Perkin Trans. 1

View full text Add to dashboard Cite

“…A novel protocol uses a cascade reaction in which three rings are constructed in a single reaction and an example is illustrated in Scheme 26. 109…”

Section: Oxygen Heterocyclesmentioning

confidence: 99%

Synthesis of heterocycles by radical cyclisation

Bowman

Cloonan

Krintel

2001

J. Chem. Soc., Perkin Trans. 1

View full text Add to dashboard Cite

Radicals and Carbohydrates

Pérez‐Martín

Suárez

2012

Encyclopedia of Radicals in Chemistry, Biology and Materials

View full text Add to dashboard Cite

show abstract

Tin Hydrides and Functional Group Transformations

Jasch

Heinrich

2012

Encyclopedia of Radicals in Chemistry, Biology and Materials

View full text Add to dashboard Cite

Tin hydrides have played an important role in the development of radical chemistry. Despite their comparatively late discovery as reagents for radical reactions in the late 1950s, they have since then had a tremendous impact. After a short historical introduction including two milestones in tin hydride radical chemistry, an overview is given of the manifold applications tin hydrides are useful for. Starting from the preparation of the classic tin hydrides, new variants are presented along with their advantages over the traditional reagents. In relation to simple radical reductions, for which tin hydrides are popular reagents because of their hydrogen‐donor abilities, we show which functional groups are suited for the tin‐mediated generation of radicals. If those radicals are not immediately reduced by the tin hydride, a large number of group transformations can be performed ranging from simple cyclizations to complex rearrangements or domino reactions.

show abstract

Catalytic tin radical mediated tricyclisations. Part 2 †‡

Cited by 7 publications

References 28 publications

Synthesis of heterocycles by radical cyclisation

Synthesis of heterocycles by radical cyclisation

Radicals and Carbohydrates

Tin Hydrides and Functional Group Transformations

Contact Info

Product

Resources

About