Asymmetric Synthesis of Polyfunctionalized Pyrrolidines and Related Alkaloids
Abstract This account describes our recent studies on the development of a general method of preparing polyfunctionalized pyrrolidine, indolizidine, pyrrolizidine and pyrrolo[1,2-A]azepines and their related alkaloids. 1 Introduction 2 Tandem Vinyl Epoxide Aminolysis/Ring-Closing Metathesis 3 All R...
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Veröffentlicht in: | Synlett 2004-12, Vol.2004 (15), p.2670-2680 |
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container_title | Synlett |
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creator | Pyne, Stephen G. Davis, Andrew S. Gates, Nicole J. Hartley, Joseph P. Lindsay, Karl B. Machan, Theeraphan Tang, Minyan |
description | Abstract
This account describes our recent studies on the development of a general method of preparing polyfunctionalized pyrrolidine, indolizidine, pyrrolizidine and pyrrolo[1,2-A]azepines and their related alkaloids.
1 Introduction
2 Tandem Vinyl Epoxide Aminolysis/Ring-Closing Metathesis
3 All Routes Lead to Oxazolidinones
4 SYN-Dihydroxylation Reactions of 2,5-Dihydropyrroles, Indolizidines and Pyrrolo[1,2-C]oxazol-3-ones
5 Asymmetric Synthesis of Swainsonine and Epiaustralines
6 Synthesis of 1,2-Amino Alcohols and Putative Uniflorine A Using the Petasis Reaction
7 Croomine Revisited |
doi_str_mv | 10.1055/s-2004-834801 |
format | Article |
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This account describes our recent studies on the development of a general method of preparing polyfunctionalized pyrrolidine, indolizidine, pyrrolizidine and pyrrolo[1,2-A]azepines and their related alkaloids.
1 Introduction
2 Tandem Vinyl Epoxide Aminolysis/Ring-Closing Metathesis
3 All Routes Lead to Oxazolidinones
4 SYN-Dihydroxylation Reactions of 2,5-Dihydropyrroles, Indolizidines and Pyrrolo[1,2-C]oxazol-3-ones
5 Asymmetric Synthesis of Swainsonine and Epiaustralines
6 Synthesis of 1,2-Amino Alcohols and Putative Uniflorine A Using the Petasis Reaction
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This account describes our recent studies on the development of a general method of preparing polyfunctionalized pyrrolidine, indolizidine, pyrrolizidine and pyrrolo[1,2-A]azepines and their related alkaloids.
1 Introduction
2 Tandem Vinyl Epoxide Aminolysis/Ring-Closing Metathesis
3 All Routes Lead to Oxazolidinones
4 SYN-Dihydroxylation Reactions of 2,5-Dihydropyrroles, Indolizidines and Pyrrolo[1,2-C]oxazol-3-ones
5 Asymmetric Synthesis of Swainsonine and Epiaustralines
6 Synthesis of 1,2-Amino Alcohols and Putative Uniflorine A Using the Petasis Reaction
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This account describes our recent studies on the development of a general method of preparing polyfunctionalized pyrrolidine, indolizidine, pyrrolizidine and pyrrolo[1,2-A]azepines and their related alkaloids.
1 Introduction
2 Tandem Vinyl Epoxide Aminolysis/Ring-Closing Metathesis
3 All Routes Lead to Oxazolidinones
4 SYN-Dihydroxylation Reactions of 2,5-Dihydropyrroles, Indolizidines and Pyrrolo[1,2-C]oxazol-3-ones
5 Asymmetric Synthesis of Swainsonine and Epiaustralines
6 Synthesis of 1,2-Amino Alcohols and Putative Uniflorine A Using the Petasis Reaction
7 Croomine Revisited</abstract><doi>10.1055/s-2004-834801</doi><tpages>11</tpages></addata></record> |
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title | Asymmetric Synthesis of Polyfunctionalized Pyrrolidines and Related Alkaloids |
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