Melamine-formaldehyde resin supported H + -catalyzed three-component synthesis of 1,8-dioxo-decahydroacridine derivatives in water and under solvent-free conditions

Abstract A convenient and practical synthesis of 1,8-dioxo-decahydroacridine derivatives using various aldehydes, 5,5-dimethyl-1,3-cyclohexanedione and thiourea in water, was successfully carried out in the presence of melamine-formaldehyde resin supported H + (MFRH) as a catalyst. Under solvent-fre...

Full description

Saved in:
Bibliographic Details
Published inHeterocyclic communications Vol. 19; no. 1; pp. 57 - 63
Main Authors Rezaei, Ramin, Khalifeh, Reza, Rajabzadeh, Maryam, Dorosty, Liela, Doroodmand, Mohammad Mahdi
Format Journal Article
LanguageEnglish
Published Berlin Walter de Gruyter GmbH 01.03.2013
Online AccessGet full text

Cover

Loading…
Abstract Abstract A convenient and practical synthesis of 1,8-dioxo-decahydroacridine derivatives using various aldehydes, 5,5-dimethyl-1,3-cyclohexanedione and thiourea in water, was successfully carried out in the presence of melamine-formaldehyde resin supported H + (MFRH) as a catalyst. Under solvent-free conditions, rapid and efficient synthesis of 1,8-dioxo-decahydroacridine and N -substituted 1,8-dioxo-decahydroacridine derivatives could also be achieved using ammonium acetate and aromatic amines as the nitrogen source.
AbstractList A convenient and practical synthesis of 1,8-dioxo-decahydroacridine derivatives using various aldehydes, 5,5-dimethyl-1,3-cyclohexanedione and thiourea in water, was successfully carried out in the presence of melamine-formaldehyde resin supported H+ (MFRH) as a catalyst. Under solvent-free conditions, rapid and efficient synthesis of 1,8-dioxo-decahydroacridine and N-substituted 1,8-dioxo-decahydroacridine derivatives could also be achieved using ammonium acetate and aromatic amines as the nitrogen source. [PUBLICATION ABSTRACT]
Abstract A convenient and practical synthesis of 1,8-dioxo-decahydroacridine derivatives using various aldehydes, 5,5-dimethyl-1,3-cyclohexanedione and thiourea in water, was successfully carried out in the presence of melamine-formaldehyde resin supported H + (MFRH) as a catalyst. Under solvent-free conditions, rapid and efficient synthesis of 1,8-dioxo-decahydroacridine and N -substituted 1,8-dioxo-decahydroacridine derivatives could also be achieved using ammonium acetate and aromatic amines as the nitrogen source.
Author Doroodmand, Mohammad Mahdi
Rezaei, Ramin
Dorosty, Liela
Rajabzadeh, Maryam
Khalifeh, Reza
Author_xml – sequence: 1
  givenname: Ramin
  surname: Rezaei
  fullname: Rezaei, Ramin
  organization: Department of Chemistry, Islamic Azad University, Firouzabad Branch, 74715, Iran
– sequence: 2
  givenname: Reza
  surname: Khalifeh
  fullname: Khalifeh, Reza
  organization: Department of Chemistry, Shiraz University of Technology, Shiraz, 75555-313, Iran
– sequence: 3
  givenname: Maryam
  surname: Rajabzadeh
  fullname: Rajabzadeh, Maryam
  organization: Department of Chemistry, Islamic Azad University, Firouzabad Branch, 74715, Iran
– sequence: 4
  givenname: Liela
  surname: Dorosty
  fullname: Dorosty, Liela
  organization: Department of Chemistry, Islamic Azad University, Firouzabad Branch, 74715, Iran
– sequence: 5
  givenname: Mohammad Mahdi
  surname: Doroodmand
  fullname: Doroodmand, Mohammad Mahdi
BookMark eNotUctOBCEQJEYTV92bH0DiUVEYmGU4GuMr0XjR84SFJoOZhRHY1fV7_FDZaF86na6u6lQdof0QAyB0yugla1l7NRjSUNYQSlu-h2YNU4xQpuQ-mlGpOKFNxw_RPOd3Wkso1ko6Qz_PMOqVD0BcTCs9Whi2FnCC7APO62mKqYDFD_gcE6OLHrffdSxDAiAmrqb6Qyg4b0MZ6knG0WF20RHr41ckFoyudClqk7ytIthC8htd_AYyrgKfukDCOli8DnWFcxw3lY-4So9NDNYXH0M-QQdOjxnm__0Yvd3dvt48kKeX-8eb6ydiOGWFLK1caK6FWLiGUq0NOCm1aJadEGrRuQUHpZiyEhxlrRIV33aCGgOKV7cUP0Znf7xTih9ryKV_j-sUqmRfLRYdk1J1FXXxhzIp5pzA9VPyK522PaM7XNsPpt9F0e-i4L9Gl4Ci
CitedBy_id crossref_primary_10_1016_j_msec_2019_109975
crossref_primary_10_1080_10406638_2016_1207687
crossref_primary_10_1007_s11164_023_05213_1
crossref_primary_10_1039_C5RA06441D
crossref_primary_10_1039_C7NJ03281A
crossref_primary_10_3390_catal12080829
crossref_primary_10_1007_s11164_022_04851_1
crossref_primary_10_1016_j_ijbiomac_2019_12_059
crossref_primary_10_1007_s11164_021_04643_z
crossref_primary_10_1016_j_jfca_2022_104802
crossref_primary_10_1080_10406638_2019_1616305
crossref_primary_10_2174_0113852728264228231013074432
crossref_primary_10_1002_slct_201600719
crossref_primary_10_1080_01932691_2019_1614460
crossref_primary_10_1080_00397911_2015_1109127
crossref_primary_10_1016_j_jece_2022_108854
crossref_primary_10_1080_10406638_2018_1481115
crossref_primary_10_1016_j_catcom_2023_106776
crossref_primary_10_1080_10406638_2018_1521846
crossref_primary_10_1080_00397911_2017_1409898
crossref_primary_10_1007_s11164_023_05125_0
crossref_primary_10_1016_j_diamond_2019_107661
crossref_primary_10_1038_s41598_023_49632_x
crossref_primary_10_1002_ajoc_202100286
ContentType Journal Article
Copyright Copyright Walter de Gruyter GmbH Mar 2013
Copyright_xml – notice: Copyright Walter de Gruyter GmbH Mar 2013
DBID AAYXX
CITATION
DOI 10.1515/hc-2012-0053
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList
CrossRef
DeliveryMethod fulltext_linktorsrc
EISSN 2191-0197
EndPage 63
ExternalDocumentID 3272328951
10_1515_hc_2012_0053
GroupedDBID 0R~
4.4
5GY
9-L
AAFPC
AAFWJ
AAQCX
AASQH
AASQN
AAWFC
AAXMT
AAYXX
ABAOT
ABAQN
ABDBF
ABFKT
ABIQR
ABLVI
ABRQL
ABUVI
ABXMZ
ACGFS
ACIWK
ACXLN
ACZBO
ADALX
ADGQD
ADGYE
ADOZN
AEJTT
AENEX
AEQDQ
AEXIE
AFAUI
AFBAA
AFCXV
AFGNR
AFPKN
AFQUK
AHGSO
AIERV
AIKXB
AJATJ
AJPIC
AKXKS
ALMA_UNASSIGNED_HOLDINGS
AMAVY
BAKPI
BBCWN
BBDJO
CITATION
DA2
EAP
EBS
EJD
ESX
GROUPED_DOAJ
HZ~
IY9
O9-
OK1
PQQKQ
QD8
RDG
SA.
ID FETCH-LOGICAL-c301t-bd76a3a446f200aacef77a42b844968f63e9919d7ef01594bd75840cce9319193
ISSN 0793-0283
IngestDate Thu Oct 10 16:03:41 EDT 2024
Fri Aug 23 00:38:45 EDT 2024
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c301t-bd76a3a446f200aacef77a42b844968f63e9919d7ef01594bd75840cce9319193
OpenAccessLink https://www.degruyter.com/document/doi/10.1515/hc-2012-0053/pdf
PQID 1514817798
PQPubID 2030121
PageCount 7
ParticipantIDs proquest_journals_1514817798
crossref_primary_10_1515_hc_2012_0053
PublicationCentury 2000
PublicationDate 2013-03-01
20130301
PublicationDateYYYYMMDD 2013-03-01
PublicationDate_xml – month: 03
  year: 2013
  text: 2013-03-01
  day: 01
PublicationDecade 2010
PublicationPlace Berlin
PublicationPlace_xml – name: Berlin
PublicationTitle Heterocyclic communications
PublicationYear 2013
Publisher Walter de Gruyter GmbH
Publisher_xml – name: Walter de Gruyter GmbH
SSID ssj0000491570
Score 2.1055498
Snippet Abstract A convenient and practical synthesis of 1,8-dioxo-decahydroacridine derivatives using various aldehydes, 5,5-dimethyl-1,3-cyclohexanedione and...
A convenient and practical synthesis of 1,8-dioxo-decahydroacridine derivatives using various aldehydes, 5,5-dimethyl-1,3-cyclohexanedione and thiourea in...
SourceID proquest
crossref
SourceType Aggregation Database
StartPage 57
Title Melamine-formaldehyde resin supported H + -catalyzed three-component synthesis of 1,8-dioxo-decahydroacridine derivatives in water and under solvent-free conditions
URI https://www.proquest.com/docview/1514817798
Volume 19
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Nb9NAEF1F7YULAgGiUNAe6ClsSZy11z6Wqo2FmlYqicjN2i8rQW1cOQng_Bx-Gr-EmbVju7Qg4GJZXsvOel5m3o7ezBLyxgQKwiDXzO_1LeMp2EL1tWKG-9byQah6LuE2Og_iCf8w9aedzo-Wamm9Uod6c29dyf9YFa6BXbFK9h8sWz8ULsA52BeOYGE4_pWNRxbsCTSROeZ5ZeysMLgNCqz_u8v1jetZbrrxgfeeuTRNsbEol8ytZSglzxYoBFgWCyCBVV8S8GvHITPz7FvGjNUSHoglV_ncIBs1MKkvrlO4U9F-ldhhETPvWImWd2GyqJ5kKbwA5exm3mQDK_4bo_om04XG3tq6XZzSaO7tRlqnMbjEydURYYZVZHZWYmJTR5NL-VmqjTTlyEjmhbyu2XmGNS1lTn5ur2Q7xYHbTQzaKY5PTjgAc-wO83WBp8NrFbccpUANolduiHNo3TVwxJgmKbW_taeP7iC6dNtlj-w70cR3jTdmGkCHApaeP2ii5lYpcH6RnE7OzpLxyXR8e7QkCZ4AzhpGWOW_68EPBS-8exQPP17UmUBYo_V9t6thPZGqQgPe_6799tvc6TZ1cHxo_Ig8rBYy9KhE5WPSsYsn5Pu9iKQOkbRGJI27DR7pL3ikNR5pltL-29-ikbbQSOHxDo0U0EgdGmkbjbRB41MyOT0ZH8es2gWEaQg-K6aMCORAch6k8N-XUttUCMk9FXIeBWEaDCyscSIjbArUNuJwP5DqntY2gvAC65NnZGcBE3hOqOcpKVNPpIHvBAphZJSRPWHBSoL7Zo8cbL9vclM2e0lwkQx2SGY6QTskaIc9sr_9-EnlDpZ4Fw_7QkThiz8PvyQPGpDvk51VvravgNmu1OsKGj8B0f2vHg
link.rule.ids 315,783,787,27936,27937
linkProvider Walter de Gruyter
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Melamine-formaldehyde+resin+supported+H%2B-catalyzed+three-component+synthesis+of+1%2C8-dioxo-decahydroacridine+derivatives+in+water+and+under+solvent-free+conditions&rft.jtitle=Heterocyclic+communications&rft.au=Rezaei%2C+Ramin&rft.au=Khalifeh%2C+Reza&rft.au=Rajabzadeh%2C+Maryam&rft.au=Dorosty%2C+Liela&rft.date=2013-03-01&rft.pub=Walter+de+Gruyter+GmbH&rft.issn=0793-0283&rft.eissn=2191-0197&rft.volume=19&rft.issue=1&rft.spage=57&rft_id=info:doi/10.1515%2Fhc-2012-0053&rft.externalDBID=NO_FULL_TEXT&rft.externalDocID=3272328951
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0793-0283&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0793-0283&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0793-0283&client=summon