Cobalt-catalyzed chelation-assisted insertion of C-C multiple bonds into C(sp2)-H bonds
In this thesis, I describe chelation-assisted cobalt-catalyzed insertion of C–C multiple bond into C(sp2)–H bond. Chapter 1 describes a brief review of a major developments of insertion of C–C multiple bond into C(sp2)–H bond. Chapter 2 describes aldimine-directed cobalt-catalyzed hydroarylation of...
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sg-ntu-dr.10356-622062023-02-28T23:37:50Z Cobalt-catalyzed chelation-assisted insertion of C-C multiple bonds into C(sp2)-H bonds Yamakawa, Takeshi Yoshikai Naohiko School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis In this thesis, I describe chelation-assisted cobalt-catalyzed insertion of C–C multiple bond into C(sp2)–H bond. Chapter 1 describes a brief review of a major developments of insertion of C–C multiple bond into C(sp2)–H bond. Chapter 2 describes aldimine-directed cobalt-catalyzed hydroarylation of aromatic aldimines with alkynes. The obtained ortho-alkenylated benzaldehydes are transformed into the corresponding indene and naphthalene derivatives. Chapter 3 describes annulation of -unsaturated imine and alkyne to afford 1,2-dihydropyridine under inexpensive cobalt catalysis. The reaction likely proceeds via olefinic C–H bond alkenylation followed by electrocyclization of the resulting azatriene intermediate. Chapter 4 describes cobalt-catalyzed branched-selective hydroarylation of substituted styrenes. The same catalytic system promotes isomerization of allyl, homoallyl, and bishomoallylbenzenes to the corresponding substituted styrenes and hydroarylation of the resulting -substituted styrenes to afford the corresponding 1,1-diarylalkanes. DOCTOR OF PHILOSOPHY (SPMS) 2015-02-25T07:47:04Z 2015-02-25T07:47:04Z 2014 2014 Thesis Yamakawa, T. (2014). Cobalt-catalyzed chelation-assisted insertion of C-C multiple bonds into C(sp2)-H bonds. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/62206 10.32657/10356/62206 en 161 p. application/pdf |
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DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis Yamakawa, Takeshi Cobalt-catalyzed chelation-assisted insertion of C-C multiple bonds into C(sp2)-H bonds |
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In this thesis, I describe chelation-assisted cobalt-catalyzed insertion of C–C multiple bond into C(sp2)–H bond. Chapter 1 describes a brief review of a major developments of insertion of C–C multiple bond into C(sp2)–H bond. Chapter 2 describes aldimine-directed cobalt-catalyzed hydroarylation of aromatic aldimines with alkynes. The obtained ortho-alkenylated benzaldehydes are transformed into the corresponding indene and naphthalene derivatives. Chapter 3 describes annulation of -unsaturated imine and alkyne to afford 1,2-dihydropyridine under inexpensive cobalt catalysis. The reaction likely proceeds via olefinic C–H bond alkenylation followed by electrocyclization of the resulting azatriene intermediate. Chapter 4 describes cobalt-catalyzed branched-selective hydroarylation of substituted styrenes. The same catalytic system promotes isomerization of allyl, homoallyl, and bishomoallylbenzenes to the corresponding substituted styrenes and hydroarylation of the resulting -substituted styrenes to afford the corresponding 1,1-diarylalkanes. |
author2 |
Yoshikai Naohiko |
author_facet |
Yoshikai Naohiko Yamakawa, Takeshi |
format |
Theses and Dissertations |
author |
Yamakawa, Takeshi |
author_sort |
Yamakawa, Takeshi |
title |
Cobalt-catalyzed chelation-assisted insertion of C-C multiple bonds into C(sp2)-H bonds |
title_short |
Cobalt-catalyzed chelation-assisted insertion of C-C multiple bonds into C(sp2)-H bonds |
title_full |
Cobalt-catalyzed chelation-assisted insertion of C-C multiple bonds into C(sp2)-H bonds |
title_fullStr |
Cobalt-catalyzed chelation-assisted insertion of C-C multiple bonds into C(sp2)-H bonds |
title_full_unstemmed |
Cobalt-catalyzed chelation-assisted insertion of C-C multiple bonds into C(sp2)-H bonds |
title_sort |
cobalt-catalyzed chelation-assisted insertion of c-c multiple bonds into c(sp2)-h bonds |
publishDate |
2015 |
url |
https://hdl.handle.net/10356/62206 |
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1759854265101189120 |