Catalytic Gels for a Prebiotically Relevant Asymmetric Aldol Reaction in Water: From Organocatalyst Design to Hydrogel Discovery and Back Again
This paper reports an investigation into organocatalytic hydrogels as prebiotically relevant systems. Gels are interesting prebiotic reaction media, combining heterogeneous and homogeneous characteristics with a structurally organized active “solid-like” catalyst separated from the surrounding envir...
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Veröffentlicht in: | Journal of the American Chemical Society 2020-03, Vol.142 (9), p.4379-4389 |
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description | This paper reports an investigation into organocatalytic hydrogels as prebiotically relevant systems. Gels are interesting prebiotic reaction media, combining heterogeneous and homogeneous characteristics with a structurally organized active “solid-like” catalyst separated from the surrounding environment, yet in intimate contact with the solution phase and readily accessible via “liquid-like” diffusion. A simple self-assembling glutamine amide derivative 1 was initially found to catalyze a model aldol reaction between cyclohexanone and 4-nitrobenzaldehyde, but it did not maintain its gel structure during reaction. In this study, it was observed that compound 1 could react directly with the benzaldehyde to form a hydrogel in situ based on Schiff base 2 as a low-molecular-weight gelator (LMWG). This new dynamic gel is a rare example of a two-component self-assembled LMWG hydrogel and was fully characterized. It was demonstrated that glutamine amide 1 could select an optimal aldehyde component and preferentially assemble from mixtures. In the hunt for an organocatalyst, reductive conditions were applied to the Schiff base to yield secondary amine 3, which is also a highly effective hydrogelator at very low loadings with a high degree of nanoscale order. Most importantly, the hydrogel based on 3 catalyzed the prebiotically relevant aldol dimerization of glycolaldehyde to give threose and erythrose. In buffered conditions, this reaction gave excellent conversions, good diastereoselectivity, and some enantioselectivity. Catalysis using the hydrogel of 3 was much better than that using non-assembled 3demonstrating a clear benefit of self-assembly. The results suggest that hydrogels offer a potential strategy by which prebiotic reactions can be promoted using simple, prebiotically plausible LMWGs that can selectively self-organize from complex mixtures. Such processes may have been of prebiotic importance. |
doi_str_mv | 10.1021/jacs.9b13156 |
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Gels are interesting prebiotic reaction media, combining heterogeneous and homogeneous characteristics with a structurally organized active “solid-like” catalyst separated from the surrounding environment, yet in intimate contact with the solution phase and readily accessible via “liquid-like” diffusion. A simple self-assembling glutamine amide derivative 1 was initially found to catalyze a model aldol reaction between cyclohexanone and 4-nitrobenzaldehyde, but it did not maintain its gel structure during reaction. In this study, it was observed that compound 1 could react directly with the benzaldehyde to form a hydrogel in situ based on Schiff base 2 as a low-molecular-weight gelator (LMWG). This new dynamic gel is a rare example of a two-component self-assembled LMWG hydrogel and was fully characterized. It was demonstrated that glutamine amide 1 could select an optimal aldehyde component and preferentially assemble from mixtures. In the hunt for an organocatalyst, reductive conditions were applied to the Schiff base to yield secondary amine 3, which is also a highly effective hydrogelator at very low loadings with a high degree of nanoscale order. Most importantly, the hydrogel based on 3 catalyzed the prebiotically relevant aldol dimerization of glycolaldehyde to give threose and erythrose. In buffered conditions, this reaction gave excellent conversions, good diastereoselectivity, and some enantioselectivity. Catalysis using the hydrogel of 3 was much better than that using non-assembled 3demonstrating a clear benefit of self-assembly. The results suggest that hydrogels offer a potential strategy by which prebiotic reactions can be promoted using simple, prebiotically plausible LMWGs that can selectively self-organize from complex mixtures. Such processes may have been of prebiotic importance.</description><identifier>ISSN: 0002-7863</identifier><identifier>ISSN: 1520-5126</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/jacs.9b13156</identifier><identifier>PMID: 32023044</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Acetaldehyde - analogs & derivatives ; Acetaldehyde - chemistry ; benzaldehyde ; Benzaldehydes - chemistry ; Catalysis ; catalytic activity ; cyclohexanones ; Cyclohexanones - chemistry ; diastereoselectivity ; dimerization ; enantioselectivity ; erythrose ; glutamine ; Glutamine - analogs & derivatives ; hydrogels ; Hydrogels - chemistry ; organocatalysts ; prebiotics ; schiff bases ; Schiff Bases - chemical synthesis ; secondary amines ; Stereoisomerism ; Tetroses - chemical synthesis</subject><ispartof>Journal of the American Chemical Society, 2020-03, Vol.142 (9), p.4379-4389</ispartof><rights>Copyright © 2020 American Chemical Society 2020 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a553t-7562a9fea5eca0dade6188b49d9e801a0d94171b0c8d1a35179dcc8efa809e1a3</citedby><cites>FETCH-LOGICAL-a553t-7562a9fea5eca0dade6188b49d9e801a0d94171b0c8d1a35179dcc8efa809e1a3</cites><orcidid>0000-0002-9881-2714</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jacs.9b13156$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jacs.9b13156$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,776,780,881,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32023044$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hawkins, Kirsten</creatorcontrib><creatorcontrib>Patterson, Anna K</creatorcontrib><creatorcontrib>Clarke, Paul A</creatorcontrib><creatorcontrib>Smith, David K</creatorcontrib><title>Catalytic Gels for a Prebiotically Relevant Asymmetric Aldol Reaction in Water: From Organocatalyst Design to Hydrogel Discovery and Back Again</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>This paper reports an investigation into organocatalytic hydrogels as prebiotically relevant systems. Gels are interesting prebiotic reaction media, combining heterogeneous and homogeneous characteristics with a structurally organized active “solid-like” catalyst separated from the surrounding environment, yet in intimate contact with the solution phase and readily accessible via “liquid-like” diffusion. A simple self-assembling glutamine amide derivative 1 was initially found to catalyze a model aldol reaction between cyclohexanone and 4-nitrobenzaldehyde, but it did not maintain its gel structure during reaction. In this study, it was observed that compound 1 could react directly with the benzaldehyde to form a hydrogel in situ based on Schiff base 2 as a low-molecular-weight gelator (LMWG). This new dynamic gel is a rare example of a two-component self-assembled LMWG hydrogel and was fully characterized. It was demonstrated that glutamine amide 1 could select an optimal aldehyde component and preferentially assemble from mixtures. In the hunt for an organocatalyst, reductive conditions were applied to the Schiff base to yield secondary amine 3, which is also a highly effective hydrogelator at very low loadings with a high degree of nanoscale order. Most importantly, the hydrogel based on 3 catalyzed the prebiotically relevant aldol dimerization of glycolaldehyde to give threose and erythrose. In buffered conditions, this reaction gave excellent conversions, good diastereoselectivity, and some enantioselectivity. Catalysis using the hydrogel of 3 was much better than that using non-assembled 3demonstrating a clear benefit of self-assembly. The results suggest that hydrogels offer a potential strategy by which prebiotic reactions can be promoted using simple, prebiotically plausible LMWGs that can selectively self-organize from complex mixtures. Such processes may have been of prebiotic importance.</description><subject>Acetaldehyde - analogs & derivatives</subject><subject>Acetaldehyde - chemistry</subject><subject>benzaldehyde</subject><subject>Benzaldehydes - chemistry</subject><subject>Catalysis</subject><subject>catalytic activity</subject><subject>cyclohexanones</subject><subject>Cyclohexanones - chemistry</subject><subject>diastereoselectivity</subject><subject>dimerization</subject><subject>enantioselectivity</subject><subject>erythrose</subject><subject>glutamine</subject><subject>Glutamine - analogs & derivatives</subject><subject>hydrogels</subject><subject>Hydrogels - chemistry</subject><subject>organocatalysts</subject><subject>prebiotics</subject><subject>schiff bases</subject><subject>Schiff Bases - chemical synthesis</subject><subject>secondary amines</subject><subject>Stereoisomerism</subject><subject>Tetroses - chemical synthesis</subject><issn>0002-7863</issn><issn>1520-5126</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxS0Eokvhxhn5yIEU2_mzDgekZUtbpEpFCMTRmjiT4MWxi-1dKZ-iX7leuhSQkDhZfvPzmxk_Qp5zdsKZ4K83oONJ2_GS180DsuC1YEXNRfOQLBhjoljKpjwiT2Lc5GslJH9MjkrBRMmqakFu1pDAzsloeo420sEHCvRjwM74LIK1M_2EFnfgEl3FeZowhQyvbO9troBOxjtqHP0KCcMbehb8RK_CCM7rn9Yx0VOMZnQ0eXox98GPaOmpidrvMMwUXE_fgf5OVyMY95Q8GsBGfHY4j8mXs_ef1xfF5dX5h_XqsoC6LlOxrBsB7YBQowbWQ48Nl7Kr2r5FyXiW2oovece07DmUNV-2vdYSB5Csxawck7d3vtfbbsJeo0sBrLoOZoIwKw9G_V1x5psa_U4tedXIRmSDlweD4H9sMSY15ZXQWnDot1GJVjZS1rJt_o-WObP9iFVGX92hOvgYAw73E3Gm9nGrfdzqEHfGX_y5xT38K9_frfevNn4bXP7Uf3vdAsa1tmU</recordid><startdate>20200304</startdate><enddate>20200304</enddate><creator>Hawkins, Kirsten</creator><creator>Patterson, Anna K</creator><creator>Clarke, Paul A</creator><creator>Smith, David K</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9881-2714</orcidid></search><sort><creationdate>20200304</creationdate><title>Catalytic Gels for a Prebiotically Relevant Asymmetric Aldol Reaction in Water: From Organocatalyst Design to Hydrogel Discovery and Back Again</title><author>Hawkins, Kirsten ; Patterson, Anna K ; Clarke, Paul A ; Smith, David K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a553t-7562a9fea5eca0dade6188b49d9e801a0d94171b0c8d1a35179dcc8efa809e1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acetaldehyde - analogs & derivatives</topic><topic>Acetaldehyde - chemistry</topic><topic>benzaldehyde</topic><topic>Benzaldehydes - chemistry</topic><topic>Catalysis</topic><topic>catalytic activity</topic><topic>cyclohexanones</topic><topic>Cyclohexanones - chemistry</topic><topic>diastereoselectivity</topic><topic>dimerization</topic><topic>enantioselectivity</topic><topic>erythrose</topic><topic>glutamine</topic><topic>Glutamine - analogs & derivatives</topic><topic>hydrogels</topic><topic>Hydrogels - chemistry</topic><topic>organocatalysts</topic><topic>prebiotics</topic><topic>schiff bases</topic><topic>Schiff Bases - chemical synthesis</topic><topic>secondary amines</topic><topic>Stereoisomerism</topic><topic>Tetroses - chemical synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hawkins, Kirsten</creatorcontrib><creatorcontrib>Patterson, Anna K</creatorcontrib><creatorcontrib>Clarke, Paul A</creatorcontrib><creatorcontrib>Smith, David K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hawkins, Kirsten</au><au>Patterson, Anna K</au><au>Clarke, Paul A</au><au>Smith, David K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catalytic Gels for a Prebiotically Relevant Asymmetric Aldol Reaction in Water: From Organocatalyst Design to Hydrogel Discovery and Back Again</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2020-03-04</date><risdate>2020</risdate><volume>142</volume><issue>9</issue><spage>4379</spage><epage>4389</epage><pages>4379-4389</pages><issn>0002-7863</issn><issn>1520-5126</issn><eissn>1520-5126</eissn><abstract>This paper reports an investigation into organocatalytic hydrogels as prebiotically relevant systems. Gels are interesting prebiotic reaction media, combining heterogeneous and homogeneous characteristics with a structurally organized active “solid-like” catalyst separated from the surrounding environment, yet in intimate contact with the solution phase and readily accessible via “liquid-like” diffusion. A simple self-assembling glutamine amide derivative 1 was initially found to catalyze a model aldol reaction between cyclohexanone and 4-nitrobenzaldehyde, but it did not maintain its gel structure during reaction. In this study, it was observed that compound 1 could react directly with the benzaldehyde to form a hydrogel in situ based on Schiff base 2 as a low-molecular-weight gelator (LMWG). This new dynamic gel is a rare example of a two-component self-assembled LMWG hydrogel and was fully characterized. It was demonstrated that glutamine amide 1 could select an optimal aldehyde component and preferentially assemble from mixtures. In the hunt for an organocatalyst, reductive conditions were applied to the Schiff base to yield secondary amine 3, which is also a highly effective hydrogelator at very low loadings with a high degree of nanoscale order. Most importantly, the hydrogel based on 3 catalyzed the prebiotically relevant aldol dimerization of glycolaldehyde to give threose and erythrose. In buffered conditions, this reaction gave excellent conversions, good diastereoselectivity, and some enantioselectivity. Catalysis using the hydrogel of 3 was much better than that using non-assembled 3demonstrating a clear benefit of self-assembly. The results suggest that hydrogels offer a potential strategy by which prebiotic reactions can be promoted using simple, prebiotically plausible LMWGs that can selectively self-organize from complex mixtures. Such processes may have been of prebiotic importance.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>32023044</pmid><doi>10.1021/jacs.9b13156</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-9881-2714</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetaldehyde - analogs & derivatives Acetaldehyde - chemistry benzaldehyde Benzaldehydes - chemistry Catalysis catalytic activity cyclohexanones Cyclohexanones - chemistry diastereoselectivity dimerization enantioselectivity erythrose glutamine Glutamine - analogs & derivatives hydrogels Hydrogels - chemistry organocatalysts prebiotics schiff bases Schiff Bases - chemical synthesis secondary amines Stereoisomerism Tetroses - chemical synthesis |
title | Catalytic Gels for a Prebiotically Relevant Asymmetric Aldol Reaction in Water: From Organocatalyst Design to Hydrogel Discovery and Back Again |
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