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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Synlett 2004-12, Vol.2004 (15), p.2670-2680
Hauptverfasser: Pyne, Stephen G., Davis, Andrew S., Gates, Nicole J., Hartley, Joseph P., Lindsay, Karl B., Machan, Theeraphan, Tang, Minyan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2680
container_issue 15
container_start_page 2670
container_title Synlett
container_volume 2004
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
fullrecord <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_s_2004_834801</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_2004_834801</sourcerecordid><originalsourceid>FETCH-LOGICAL-c340t-ef40120a815f112128ee3c615a288001e2e97dee18ffa9cb42c8f0c86df0e4253</originalsourceid><addsrcrecordid>eNp1kMtOwzAQRS0EEuWxZJ8PwDDjOKmzrCpeUhEVj7VlnLHq4sTIThfh60lVtqxGmjka3XsYu0K4Qaiq28wFgOSqlArwiM1QlvNp1dTHbAZNWfNKoDxlZzlvAVCqBmbseZHHrqMheVu8jf2woexzEV2xjmF0u94OPvYm-B9qi_WYUgy-9T3lwvRt8UrBDNNhEb5MiL7NF-zEmZDp8m-es4_7u_flI1-9PDwtFytuSwkDJycBBRiFlUMUKBRRaWusjFBqikaCmnlLhMo509hPKaxyYFXdOiApqvKc8cNfm2LOiZz-Tr4zadQIeu9CZ713oQ8uJv76wA8bTx3pbdylqVX-B_8FO0dghg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Asymmetric Synthesis of Polyfunctionalized Pyrrolidines and Related Alkaloids</title><source>Thieme Connect Journals</source><creator>Pyne, Stephen G. ; Davis, Andrew S. ; Gates, Nicole J. ; Hartley, Joseph P. ; Lindsay, Karl B. ; Machan, Theeraphan ; Tang, Minyan</creator><creatorcontrib>Pyne, Stephen G. ; Davis, Andrew S. ; Gates, Nicole J. ; Hartley, Joseph P. ; Lindsay, Karl B. ; Machan, Theeraphan ; Tang, Minyan</creatorcontrib><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</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2004-834801</identifier><language>eng</language><subject>account</subject><ispartof>Synlett, 2004-12, Vol.2004 (15), p.2670-2680</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-ef40120a815f112128ee3c615a288001e2e97dee18ffa9cb42c8f0c86df0e4253</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2004-834801.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2004-834801$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,778,782,3006,3007,27907,27908,54542,54543</link.rule.ids></links><search><creatorcontrib>Pyne, Stephen G.</creatorcontrib><creatorcontrib>Davis, Andrew S.</creatorcontrib><creatorcontrib>Gates, Nicole J.</creatorcontrib><creatorcontrib>Hartley, Joseph P.</creatorcontrib><creatorcontrib>Lindsay, Karl B.</creatorcontrib><creatorcontrib>Machan, Theeraphan</creatorcontrib><creatorcontrib>Tang, Minyan</creatorcontrib><title>Asymmetric Synthesis of Polyfunctionalized Pyrrolidines and Related Alkaloids</title><title>Synlett</title><addtitle>Synlett</addtitle><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</description><subject>account</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp1kMtOwzAQRS0EEuWxZJ8PwDDjOKmzrCpeUhEVj7VlnLHq4sTIThfh60lVtqxGmjka3XsYu0K4Qaiq28wFgOSqlArwiM1QlvNp1dTHbAZNWfNKoDxlZzlvAVCqBmbseZHHrqMheVu8jf2woexzEV2xjmF0u94OPvYm-B9qi_WYUgy-9T3lwvRt8UrBDNNhEb5MiL7NF-zEmZDp8m-es4_7u_flI1-9PDwtFytuSwkDJycBBRiFlUMUKBRRaWusjFBqikaCmnlLhMo509hPKaxyYFXdOiApqvKc8cNfm2LOiZz-Tr4zadQIeu9CZ713oQ8uJv76wA8bTx3pbdylqVX-B_8FO0dghg</recordid><startdate>20041207</startdate><enddate>20041207</enddate><creator>Pyne, Stephen G.</creator><creator>Davis, Andrew S.</creator><creator>Gates, Nicole J.</creator><creator>Hartley, Joseph P.</creator><creator>Lindsay, Karl B.</creator><creator>Machan, Theeraphan</creator><creator>Tang, Minyan</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20041207</creationdate><title>Asymmetric Synthesis of Polyfunctionalized Pyrrolidines and Related Alkaloids</title><author>Pyne, Stephen G. ; Davis, Andrew S. ; Gates, Nicole J. ; Hartley, Joseph P. ; Lindsay, Karl B. ; Machan, Theeraphan ; Tang, Minyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-ef40120a815f112128ee3c615a288001e2e97dee18ffa9cb42c8f0c86df0e4253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>account</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pyne, Stephen G.</creatorcontrib><creatorcontrib>Davis, Andrew S.</creatorcontrib><creatorcontrib>Gates, Nicole J.</creatorcontrib><creatorcontrib>Hartley, Joseph P.</creatorcontrib><creatorcontrib>Lindsay, Karl B.</creatorcontrib><creatorcontrib>Machan, Theeraphan</creatorcontrib><creatorcontrib>Tang, Minyan</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pyne, Stephen G.</au><au>Davis, Andrew S.</au><au>Gates, Nicole J.</au><au>Hartley, Joseph P.</au><au>Lindsay, Karl B.</au><au>Machan, Theeraphan</au><au>Tang, Minyan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asymmetric Synthesis of Polyfunctionalized Pyrrolidines and Related Alkaloids</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2004-12-07</date><risdate>2004</risdate><volume>2004</volume><issue>15</issue><spage>2670</spage><epage>2680</epage><pages>2670-2680</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>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</abstract><doi>10.1055/s-2004-834801</doi><tpages>11</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0936-5214
ispartof Synlett, 2004-12, Vol.2004 (15), p.2670-2680
issn 0936-5214
1437-2096
language eng
recordid cdi_crossref_primary_10_1055_s_2004_834801
source Thieme Connect Journals
subjects account
title Asymmetric Synthesis of Polyfunctionalized Pyrrolidines and Related Alkaloids
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T08%3A33%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-thieme_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Asymmetric%20Synthesis%20of%20Polyfunctionalized%20Pyrrolidines%20and%20Related%20Alkaloids&rft.jtitle=Synlett&rft.au=Pyne,%20Stephen%20G.&rft.date=2004-12-07&rft.volume=2004&rft.issue=15&rft.spage=2670&rft.epage=2680&rft.pages=2670-2680&rft.issn=0936-5214&rft.eissn=1437-2096&rft_id=info:doi/10.1055/s-2004-834801&rft_dat=%3Cthieme_cross%3E10_1055_s_2004_834801%3C/thieme_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true