Syntheses of diaza[1.1.1] and [1.1.1.1] paracyclophanes by smiles rearrangement
[Display omitted] •Two strained macrocycles, diaza[1.1.1] and [1.1.1.1]paracyclophanes were synthesized.•The synthetic route is short and simple.•The molecular structures of two paracyclophanes were simulated by DFT calculations.•Diaza[1.1.1]paracyclophane is highly distorted.•Intramolecular partial...
Gespeichert in:
Veröffentlicht in: | Tetrahedron letters 2023-10, Vol.130, p.154762, Article 154762 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | 154762 |
container_title | Tetrahedron letters |
container_volume | 130 |
creator | Takemura, Hiroyuki Wakamatsu, Maho Murakami, Hiroko Iwanaga, Tetsuo Sako, Katsuya |
description | [Display omitted]
•Two strained macrocycles, diaza[1.1.1] and [1.1.1.1]paracyclophanes were synthesized.•The synthetic route is short and simple.•The molecular structures of two paracyclophanes were simulated by DFT calculations.•Diaza[1.1.1]paracyclophane is highly distorted.•Intramolecular partially overlapping MO’s were observed, which led to the sharpening of the bridging units.
Highly strained diaza[1.1.1] and [1.1.1.1]paracyclophanes were synthesized using Smiles rearrangement (paracyclophane is hereafter abbreviated as PCP). Smiles rearrangement allowed the synthesis of compounds with bridging groups, which could not be obtained using the previously reported Chapman rearrangement method. The two synthetic methods are complementary to each other and therefore useful for the synthesis of diaza[1n]PCP. However, in Chapman rearrangement, the diaza[1.1.1]PCP precursor is a rigid molecule and the precursor could not be synthesized. In contrast, the Smiles rearrangement uses a PCP-precursor rearrangement with low distortion; thus, [1.1.1]PCP can be obtained. Furthermore, the syntheses of 1a and 2 can be performed on a gram scale. However, due to their low solubility, the molecular structure could not be confirmed by crystallographic analysis; therefore, these structures were optimized by DFT calculations and discussed. |
doi_str_mv | 10.1016/j.tetlet.2023.154762 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3153594267</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0040403923004720</els_id><sourcerecordid>3153594267</sourcerecordid><originalsourceid>FETCH-LOGICAL-c288t-d08116fe5e06a959745aa69e6cc119f3aef376b4700df005f7b01665c1bf5dce3</originalsourceid><addsrcrecordid>eNp9UE1LxDAQDaLguvoPPPTopXXSNGl7EWTxCxb2oJ5EQppO3Cz9WJMo1F9vlnp25jBv4M1j3iPkkkJGgYrrXRYwdBiyHHKWUV6UIj8iC1qVLGW8osdkAVBAWgCrT8mZ9zuIJSpYkM3zNIQtevTJaJLWqh_1RrPY74ka2mTGh22vnNKT7sb9Vg2R3UyJ720XkUPlnBo-sMchnJMTozqPF39zSV7v715Wj-l68_C0ul2nOq-qkLZQUSoMcgShal6XBVdK1Ci0prQ2TKFhpWiKEqA1ANyUTTQquKaN4a1GtiRXs-7ejZ9f6IPsrdfYdfG58ctLRjnjdZGLMlKLmard6L1DI_fO9spNkoI85Cd3cs5PHvKTc37x7GY-w2jj26KTXlscNLbWoQ6yHe3_Ar_Tw3l0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3153594267</pqid></control><display><type>article</type><title>Syntheses of diaza[1.1.1] and [1.1.1.1] paracyclophanes by smiles rearrangement</title><source>Elsevier ScienceDirect Journals</source><creator>Takemura, Hiroyuki ; Wakamatsu, Maho ; Murakami, Hiroko ; Iwanaga, Tetsuo ; Sako, Katsuya</creator><creatorcontrib>Takemura, Hiroyuki ; Wakamatsu, Maho ; Murakami, Hiroko ; Iwanaga, Tetsuo ; Sako, Katsuya</creatorcontrib><description>[Display omitted]
•Two strained macrocycles, diaza[1.1.1] and [1.1.1.1]paracyclophanes were synthesized.•The synthetic route is short and simple.•The molecular structures of two paracyclophanes were simulated by DFT calculations.•Diaza[1.1.1]paracyclophane is highly distorted.•Intramolecular partially overlapping MO’s were observed, which led to the sharpening of the bridging units.
Highly strained diaza[1.1.1] and [1.1.1.1]paracyclophanes were synthesized using Smiles rearrangement (paracyclophane is hereafter abbreviated as PCP). Smiles rearrangement allowed the synthesis of compounds with bridging groups, which could not be obtained using the previously reported Chapman rearrangement method. The two synthetic methods are complementary to each other and therefore useful for the synthesis of diaza[1n]PCP. However, in Chapman rearrangement, the diaza[1.1.1]PCP precursor is a rigid molecule and the precursor could not be synthesized. In contrast, the Smiles rearrangement uses a PCP-precursor rearrangement with low distortion; thus, [1.1.1]PCP can be obtained. Furthermore, the syntheses of 1a and 2 can be performed on a gram scale. However, due to their low solubility, the molecular structure could not be confirmed by crystallographic analysis; therefore, these structures were optimized by DFT calculations and discussed.</description><identifier>ISSN: 0040-4039</identifier><identifier>EISSN: 1873-3581</identifier><identifier>DOI: 10.1016/j.tetlet.2023.154762</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>[1n]paracyclophanes ; chemical structure ; Cyclophanes ; Macrocycles ; methodology ; Smiles rearrangement ; solubility ; strains</subject><ispartof>Tetrahedron letters, 2023-10, Vol.130, p.154762, Article 154762</ispartof><rights>2023 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c288t-d08116fe5e06a959745aa69e6cc119f3aef376b4700df005f7b01665c1bf5dce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0040403923004720$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids></links><search><creatorcontrib>Takemura, Hiroyuki</creatorcontrib><creatorcontrib>Wakamatsu, Maho</creatorcontrib><creatorcontrib>Murakami, Hiroko</creatorcontrib><creatorcontrib>Iwanaga, Tetsuo</creatorcontrib><creatorcontrib>Sako, Katsuya</creatorcontrib><title>Syntheses of diaza[1.1.1] and [1.1.1.1] paracyclophanes by smiles rearrangement</title><title>Tetrahedron letters</title><description>[Display omitted]
•Two strained macrocycles, diaza[1.1.1] and [1.1.1.1]paracyclophanes were synthesized.•The synthetic route is short and simple.•The molecular structures of two paracyclophanes were simulated by DFT calculations.•Diaza[1.1.1]paracyclophane is highly distorted.•Intramolecular partially overlapping MO’s were observed, which led to the sharpening of the bridging units.
Highly strained diaza[1.1.1] and [1.1.1.1]paracyclophanes were synthesized using Smiles rearrangement (paracyclophane is hereafter abbreviated as PCP). Smiles rearrangement allowed the synthesis of compounds with bridging groups, which could not be obtained using the previously reported Chapman rearrangement method. The two synthetic methods are complementary to each other and therefore useful for the synthesis of diaza[1n]PCP. However, in Chapman rearrangement, the diaza[1.1.1]PCP precursor is a rigid molecule and the precursor could not be synthesized. In contrast, the Smiles rearrangement uses a PCP-precursor rearrangement with low distortion; thus, [1.1.1]PCP can be obtained. Furthermore, the syntheses of 1a and 2 can be performed on a gram scale. However, due to their low solubility, the molecular structure could not be confirmed by crystallographic analysis; therefore, these structures were optimized by DFT calculations and discussed.</description><subject>[1n]paracyclophanes</subject><subject>chemical structure</subject><subject>Cyclophanes</subject><subject>Macrocycles</subject><subject>methodology</subject><subject>Smiles rearrangement</subject><subject>solubility</subject><subject>strains</subject><issn>0040-4039</issn><issn>1873-3581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9UE1LxDAQDaLguvoPPPTopXXSNGl7EWTxCxb2oJ5EQppO3Cz9WJMo1F9vlnp25jBv4M1j3iPkkkJGgYrrXRYwdBiyHHKWUV6UIj8iC1qVLGW8osdkAVBAWgCrT8mZ9zuIJSpYkM3zNIQtevTJaJLWqh_1RrPY74ka2mTGh22vnNKT7sb9Vg2R3UyJ720XkUPlnBo-sMchnJMTozqPF39zSV7v715Wj-l68_C0ul2nOq-qkLZQUSoMcgShal6XBVdK1Ci0prQ2TKFhpWiKEqA1ANyUTTQquKaN4a1GtiRXs-7ejZ9f6IPsrdfYdfG58ctLRjnjdZGLMlKLmard6L1DI_fO9spNkoI85Cd3cs5PHvKTc37x7GY-w2jj26KTXlscNLbWoQ6yHe3_Ar_Tw3l0</recordid><startdate>20231025</startdate><enddate>20231025</enddate><creator>Takemura, Hiroyuki</creator><creator>Wakamatsu, Maho</creator><creator>Murakami, Hiroko</creator><creator>Iwanaga, Tetsuo</creator><creator>Sako, Katsuya</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20231025</creationdate><title>Syntheses of diaza[1.1.1] and [1.1.1.1] paracyclophanes by smiles rearrangement</title><author>Takemura, Hiroyuki ; Wakamatsu, Maho ; Murakami, Hiroko ; Iwanaga, Tetsuo ; Sako, Katsuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c288t-d08116fe5e06a959745aa69e6cc119f3aef376b4700df005f7b01665c1bf5dce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>[1n]paracyclophanes</topic><topic>chemical structure</topic><topic>Cyclophanes</topic><topic>Macrocycles</topic><topic>methodology</topic><topic>Smiles rearrangement</topic><topic>solubility</topic><topic>strains</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takemura, Hiroyuki</creatorcontrib><creatorcontrib>Wakamatsu, Maho</creatorcontrib><creatorcontrib>Murakami, Hiroko</creatorcontrib><creatorcontrib>Iwanaga, Tetsuo</creatorcontrib><creatorcontrib>Sako, Katsuya</creatorcontrib><collection>CrossRef</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Tetrahedron letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takemura, Hiroyuki</au><au>Wakamatsu, Maho</au><au>Murakami, Hiroko</au><au>Iwanaga, Tetsuo</au><au>Sako, Katsuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Syntheses of diaza[1.1.1] and [1.1.1.1] paracyclophanes by smiles rearrangement</atitle><jtitle>Tetrahedron letters</jtitle><date>2023-10-25</date><risdate>2023</risdate><volume>130</volume><spage>154762</spage><pages>154762-</pages><artnum>154762</artnum><issn>0040-4039</issn><eissn>1873-3581</eissn><abstract>[Display omitted]
•Two strained macrocycles, diaza[1.1.1] and [1.1.1.1]paracyclophanes were synthesized.•The synthetic route is short and simple.•The molecular structures of two paracyclophanes were simulated by DFT calculations.•Diaza[1.1.1]paracyclophane is highly distorted.•Intramolecular partially overlapping MO’s were observed, which led to the sharpening of the bridging units.
Highly strained diaza[1.1.1] and [1.1.1.1]paracyclophanes were synthesized using Smiles rearrangement (paracyclophane is hereafter abbreviated as PCP). Smiles rearrangement allowed the synthesis of compounds with bridging groups, which could not be obtained using the previously reported Chapman rearrangement method. The two synthetic methods are complementary to each other and therefore useful for the synthesis of diaza[1n]PCP. However, in Chapman rearrangement, the diaza[1.1.1]PCP precursor is a rigid molecule and the precursor could not be synthesized. In contrast, the Smiles rearrangement uses a PCP-precursor rearrangement with low distortion; thus, [1.1.1]PCP can be obtained. Furthermore, the syntheses of 1a and 2 can be performed on a gram scale. However, due to their low solubility, the molecular structure could not be confirmed by crystallographic analysis; therefore, these structures were optimized by DFT calculations and discussed.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.tetlet.2023.154762</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0040-4039 |
ispartof | Tetrahedron letters, 2023-10, Vol.130, p.154762, Article 154762 |
issn | 0040-4039 1873-3581 |
language | eng |
recordid | cdi_proquest_miscellaneous_3153594267 |
source | Elsevier ScienceDirect Journals |
subjects | [1n]paracyclophanes chemical structure Cyclophanes Macrocycles methodology Smiles rearrangement solubility strains |
title | Syntheses of diaza[1.1.1] and [1.1.1.1] paracyclophanes by smiles rearrangement |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T14%3A12%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Syntheses%20of%20diaza%5B1.1.1%5D%20and%20%5B1.1.1.1%5D%20paracyclophanes%20by%20smiles%20rearrangement&rft.jtitle=Tetrahedron%20letters&rft.au=Takemura,%20Hiroyuki&rft.date=2023-10-25&rft.volume=130&rft.spage=154762&rft.pages=154762-&rft.artnum=154762&rft.issn=0040-4039&rft.eissn=1873-3581&rft_id=info:doi/10.1016/j.tetlet.2023.154762&rft_dat=%3Cproquest_cross%3E3153594267%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3153594267&rft_id=info:pmid/&rft_els_id=S0040403923004720&rfr_iscdi=true |