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pro vyhledávání: '"Lindsay, Karl"'
Autor:
Lindsay, Karl B.
Publikováno v:
Access electronically.
Thesis (Ph.D.)--University of Wollongong, 2003.
Typescript. Includes bibliographical references: leaf 214-222.
Typescript. Includes bibliographical references: leaf 214-222.
Autor:
Lindsay, Karl B
Publikováno v:
University of Wollongong Thesis Collection.
The aim of this project was to develop a flexible asymmetric synthesis of 1-aza-[2+n.3.0] bicyclic ring systems (n=1,2,3). This was accomplished by the aminolysis of chiral vinyl epoxides followed by ring closing metathesis of the resulting dienes to
Externí odkaz:
http://ro.uow.edu.au/theses/167
Publikováno v:
In Tetrahedron 2009 65(52):10908-10916
Autor:
Taaning, Rolf H, Lindsay, Karl B, Schiøtt, Birgit, Daasbjerg, Kim, Skrydstrup, Troels, Taaning, Rolf Hejle
Publikováno v:
Taaning, R H, Lindsay, K B, Schiøtt, B, Daasbjerg, K, Skrydstrup, T & Taaning, R H 2009, ' Importance of C-N bond rotation in N-acyl oxazolidinones in their SmI2-promoted coupling to acrylamides ', Journal of the American Chemical Society, vol. 131, no. 29, pp. 10253-62 . https://doi.org/10.1021/ja903401y
A detailed mechanistic investigation was undertaken to determine the dominating factors of the postelectron transfer steps in the SmI(2)-promoted carbon-carbon bond forming reaction between N-acyl oxazolidinones and acrylamides. Competition experimen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb4e12c1623227c3b9a0a3aacdccfbcf
https://pure.au.dk/portal/da/publications/importance-of-cn-bond-rotation-in-nacyl-oxazolidinones-in-their-smi2promoted-coupling-to-acrylamides(c673aa19-eeed-45de-a5aa-e6e5289102ae).html
https://pure.au.dk/portal/da/publications/importance-of-cn-bond-rotation-in-nacyl-oxazolidinones-in-their-smi2promoted-coupling-to-acrylamides(c673aa19-eeed-45de-a5aa-e6e5289102ae).html
Publikováno v:
Taaning, R, Lindsay, K & Skrydstrup, T 2009, ' Some unusual reactivities in the SmI 2-mediated reductive coupling of acrylamides and acrylates with imides ', Tetrahedron, vol. 65, pp. 10908 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::ecf66e423471fde5fee10999edabce2d
https://pure.au.dk/portal/da/publications/some-unusual-reactivities-in-the-smi2mediated-reductive-coupling-of-acrylamides-and-acrylates-with-imides(6dfa2640-2143-11df-b95d-000ea68e967b).html
https://pure.au.dk/portal/da/publications/some-unusual-reactivities-in-the-smi2mediated-reductive-coupling-of-acrylamides-and-acrylates-with-imides(6dfa2640-2143-11df-b95d-000ea68e967b).html
Autor:
Taaning, Rolf Hejle, Lindsay, Karl, Schiøtt, Hanne Birgit, Daasbjerg, Kim, Skrydstrup, Troels
Publikováno v:
Taaning, R H, Lindsay, K, Schiøtt, H B, Daasbjerg, K & Skrydstrup, T 2009, ' C-N Bond Rotation in N-Acyl Oxazolidinones as the Controlling Factor in Their SmI 2-Promoted Coupling to Acrylamides ', Journal of the American Chemical Society, vol. 131, pp. 10253-10262 .
Udgivelsesdato: 2009
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::abd8c427cae26d807b45402d8ed1f36f
https://pure.au.dk/portal/da/publications/cn-bond-rotation-in-nacyl-oxazolidinones-as-the-controlling-factor-in-their-smi2promoted-coupling-to-acrylamides(35b39ec0-9c59-11de-a092-000ea68e967b).html
https://pure.au.dk/portal/da/publications/cn-bond-rotation-in-nacyl-oxazolidinones-as-the-controlling-factor-in-their-smi2promoted-coupling-to-acrylamides(35b39ec0-9c59-11de-a092-000ea68e967b).html
Publikováno v:
Taaning, R H, Lindsay, K B, Skrydstrup, T & Taaning, R H 2009, ' Some unusual reactivities in the SmI2-mediated reductive coupling of acrylamides and acrylates with imides ', Tetrahedron, vol. 65, no. 52, pp. 10908-10916 .
A serendipitous discovery of some intra-molecular enolate addition reactions following a SmI2-mediated reductive cross-coupling between imides and electron-deficient olefins leading to some novel compounds was investigated to determine the generality
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::f92be665bed5bbcdb621ae82129be3b5
https://pure.au.dk/portal/da/publications/some-unusual-reactivities-in-the-smi2mediated-reductive-coupling-of-acrylamides-and-acrylates-with-imides(17aaa60c-5f36-4ef2-8e8d-0c458899af9e).html
https://pure.au.dk/portal/da/publications/some-unusual-reactivities-in-the-smi2mediated-reductive-coupling-of-acrylamides-and-acrylates-with-imides(17aaa60c-5f36-4ef2-8e8d-0c458899af9e).html
Publikováno v:
Nielsen, L, Lindsay, K & Skrydstrup, T 2008, ' Synthesis of Silanediol Peptide Mimics ', Dublin, Ireland, 08/07/2007-13/07/2007, .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::f3f64953862d62ce385a6641f845c0a3
https://pure.au.dk/portal/da/publications/synthesis-of-silanediol-peptide-mimics(fb669970-ce46-11dc-abe4-000ea68e967b).html
https://pure.au.dk/portal/da/publications/synthesis-of-silanediol-peptide-mimics(fb669970-ce46-11dc-abe4-000ea68e967b).html
Publikováno v:
Nielsen, L, Skrydstrup, T & Lindsay, K 2008, ' Synthesis of Silanediol Peptide Mimic Precursors ', Haevichi, Jeju, Korea, Republic of, 01/06/2008-06/06/2008, .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::319de0de63abe3b27c32528835c238b3
https://pure.au.dk/portal/da/publications/synthesis-of-silanediol-peptide-mimic-precursors(b0dd84e0-8dfe-11dd-bd84-000ea68e967b).html
https://pure.au.dk/portal/da/publications/synthesis-of-silanediol-peptide-mimic-precursors(b0dd84e0-8dfe-11dd-bd84-000ea68e967b).html