Formal synthesis of (+)-crocacin C

The formal synthesis of (+)-crocacin C is reported. The approach described takes advantage of a highly regioselective epoxide cuprate addition and a diastereoselective Overman rearrangement. The synthesis is practical and amenable to scale up.

Saved in:

Bibliographic Details
Published in:	Tetrahedron letters Vol. 53; no. 16; pp. 2114 - 2116
Main Authors:	Pasqua, Adele E., Ferrari, Frank D., Crawford, James J., Marquez, Rodolfo
Format:	Journal Article
Language:	English
Published:	Elsevier Ltd 18-04-2012
Subjects:	COPPER OXIDE Crocacins Cuprates FABRICATION Formal synthesis Overman rearrangement Synthesis (chemistry) Tetrahedrons Formal synthesis Crocacins Overman rearrangement
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Abstract	The formal synthesis of (+)-crocacin C is reported. The approach described takes advantage of a highly regioselective epoxide cuprate addition and a diastereoselective Overman rearrangement. The synthesis is practical and amenable to scale up.
AbstractList	The formal synthesis of (+)-crocacin C is reported. The approach described takes advantage of a highly regioselective epoxide cuprate addition and a diastereoselective Overman rearrangement. The synthesis is practical and amenable to scale up.
Author	Marquez, Rodolfo Pasqua, Adele E. Ferrari, Frank D. Crawford, James J.
Author_xml	– sequence: 1 givenname: Adele E. surname: Pasqua fullname: Pasqua, Adele E. organization: WestCHEM School of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK – sequence: 2 givenname: Frank D. surname: Ferrari fullname: Ferrari, Frank D. organization: WestCHEM School of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK – sequence: 3 givenname: James J. surname: Crawford fullname: Crawford, James J. organization: Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA – sequence: 4 givenname: Rodolfo surname: Marquez fullname: Marquez, Rodolfo email: rudi.marquez@glasgow.ac.uk, r.marquez@chem.gla.ac.uk organization: WestCHEM School of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK
BookMark	eNp9kEFLxDAQhYOs4K76DzwUTyvSOmnSJr0IsrgqLHjRc0iTKWbptmuSFfbfm6WeHR7M5b3HzLcgs2EckJAbCgUFWj9si4ixx1iUQMsCknhzRuZUCpazStIZmQNwyDmw5oIsQthCmlrCnNyuR7_TfRaOQ_zC4EI2dtny_i43fjTauCFbXZHzTvcBr__2JflcP3-sXvPN-8vb6mmTG8aamEu0dUdbxpltDAcJlkKpmQBRad5KK1pJmaGdYEAb5G1NbSVYLWxrEFC07JIsp969H78PGKLauWCw7_WA4yEoKjivZckrlqx8sqYrQ_DYqb13O-2PioI6IVFbNSFRJyQKkniTYo9TDNMbPw69CsbhYNA6jyYqO7r_C34Bm99rCA
CitedBy_id	crossref_primary_10_1016_j_tet_2015_09_057 crossref_primary_10_1016_j_bmc_2015_01_008 crossref_primary_10_1016_j_tet_2012_09_068 crossref_primary_10_1039_C4QO00332B crossref_primary_10_1016_j_tetlet_2017_06_011 crossref_primary_10_1246_bcsj_20140271 crossref_primary_10_1021_jo301210f
Cites_doi	10.1021/ol103114w 10.1021/ja00545a044 10.1021/ol070336e 10.1135/cccc20051696 10.1021/ol016845c 10.1021/ol0064664 10.1021/ol017092x 10.1021/jo800906p 10.1071/CH03026 10.15227/orgsyn.082.0134 10.1016/S0040-4039(00)02002-5 10.1021/ol035227o 10.1080/00304940903188084 10.1039/b901797f 10.1016/j.bmc.2010.03.003 10.1039/p19950000785 10.1016/j.bmc.2008.10.030 10.1021/jo047732k 10.1039/c0cc05178k 10.1016/j.tet.2011.07.033 10.1016/j.tet.2007.06.081 10.1021/jm061123i 10.1021/jo902582w 10.2533/000942903777678669 10.1016/S0040-4020(01)00940-1 10.1016/j.tet.2008.01.139 10.7164/antibiotics.47.881
ContentType	Journal Article
Copyright	2012 Elsevier Ltd
Copyright_xml	– notice: 2012 Elsevier Ltd
DBID	AAYXX CITATION 7SR 7U5 8BQ 8FD H8G JG9 L7M
DOI	10.1016/j.tetlet.2012.02.049
DatabaseName	CrossRef Engineered Materials Abstracts Solid State and Superconductivity Abstracts METADEX Technology Research Database Copper Technical Reference Library Materials Research Database Advanced Technologies Database with Aerospace
DatabaseTitle	CrossRef Materials Research Database Copper Technical Reference Library Engineered Materials Abstracts Technology Research Database Solid State and Superconductivity Abstracts Advanced Technologies Database with Aerospace METADEX
DatabaseTitleList	Materials Research Database
DeliveryMethod	fulltext_linktorsrc
Discipline	Chemistry
EISSN	1873-3581
EndPage	2116
ExternalDocumentID	10_1016_j_tetlet_2012_02_049 S0040403912002857
GroupedDBID	--- --K --M -ET -~X .~1 0R~ 123 1B1 1RT 1~. 1~5 4.4 457 4G. 53G 5VS 7-5 71M 85S 8P~ 9JM 9JN AABNK AACTN AAEDT AAEDW AAIAV AAIKJ AAKOC AALRI AAOAW AAQFI AARLI AATCM AAXUO ABFNM ABFRF ABGSF ABJNI ABMAC ABPPZ ABUDA ABXDB ABYKQ ABZDS ACBEA ACDAQ ACGFS ACNCT ACNNM ACRLP ADBBV ADECG ADEZE ADMUD ADUVX AEBSH AEFWE AEHWI AEKER AENEX AFKWA AFTJW AFXIZ AFZHZ AGHFR AGUBO AGYEJ AHHHB AIEXJ AIKHN AITUG AJBFU AJOXV AJSZI ALCLG ALMA_UNASSIGNED_HOLDINGS AMFUW AMRAJ AXJTR BKOJK BLXMC CS3 DOVZS DU5 EBS EFJIC EFLBG EJD EO8 EO9 EP2 EP3 F5P FDB FIRID FLBIZ FNPLU FYGXN G-Q GBLVA HZ~ IH2 J1W K-O KOM M2Z M41 MO0 N9A O-L O9- OAUVE OGGZJ OZT P-8 P-9 P2P PC. Q38 RIG RNS ROL RPZ SCC SDF SDG SDP SES SPC SPCBC SSK SSP SSU SSZ T5K TN5 TWZ WH7 XPP XSW YK3 YR2 ZMT ~02 ~G- ~KM .GJ .HR 186 29Q 3EH 6TJ AAHBH AAQXK AAXKI AAYOK AAYXX ABDPE ACBNA ACKIV ADVLN AFFNX AFJKZ AGRDE AKRWK ASPBG AVWKF AZFZN CITATION D0S FEDTE FGOYB HMS HVGLF IHE MVM OHT R2- SCB SEW SOC UQL WUQ XJT Y6R YQJ ZCG ZKB ZXP 7SR 7U5 8BQ 8FD H8G JG9 L7M
ID	FETCH-LOGICAL-c339t-8ed6f1b343d9c4080d102a37075a4b8d7b813c1f73019e4b61d57367dbce0e7b3
ISSN	0040-4039
IngestDate	Fri Oct 25 01:57:00 EDT 2024 Fri Nov 22 00:04:17 EST 2024 Fri Feb 23 02:27:20 EST 2024
IsPeerReviewed	true
IsScholarly	true
Issue	16
Keywords	Formal synthesis Crocacins Overman rearrangement
Language	English
LinkModel	OpenURL
MergedId	FETCHMERGED-LOGICAL-c339t-8ed6f1b343d9c4080d102a37075a4b8d7b813c1f73019e4b61d57367dbce0e7b3
Notes	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
PQID	1744682453
PQPubID	23500
PageCount	3
ParticipantIDs	proquest_miscellaneous_1744682453 crossref_primary_10_1016_j_tetlet_2012_02_049 elsevier_sciencedirect_doi_10_1016_j_tetlet_2012_02_049
PublicationCentury	2000
PublicationDate	2012-04-18
PublicationDateYYYYMMDD	2012-04-18
PublicationDate_xml	– month: 04 year: 2012 text: 2012-04-18 day: 18
PublicationDecade	2010
PublicationTitle	Tetrahedron letters
PublicationYear	2012
Publisher	Elsevier Ltd
Publisher_xml	– name: Elsevier Ltd
References	Beşev, Brehm, Fürstner (b0110) 2005; 70 Crowley, Berry, Cromartie, Daldal, Godfrey, Lee, Phillips, Taylor, Viner, Crowley, Godfrey, Viner, Crowley, Aspinall, Gillen, Godfrey, Devillers, Munns, Sageot, Swanborough, Worthington, Williams, Nising, Hillebrand, Rodefeld (b0010) 2008; 16 b0195 Villa, Targett, Barnes, Whittingham, Marquez, Mathieson, Crawford, Schmidtmann, Marquez, Pasqua, Crawford, Marquez, Sewell, Villa, Matheson, Whittingham, Marquez (b0120) 2007; 9 Dias, de Oliveira, Dias, de Oliveira, Vilcachagua, Nigsch (b0075) 2001; 3 Kawai, Mahadeo, Uenishi (b0155) 2007; 63 Feutrill, Lilly, Rizzacasa, Feutrill, Lilly, Rizzacasa, Feutrill, Rizzacasa, Feutrill, Lilly, White, Rizzacasa (b0035) 2000; 2 Candy, Audran, Bienayme, Bressy, Pons (b0115) 2010; 75 Nakamura, Tanino, Masaaki (b0145) 2003; 5 Anderson, Overman, Watson, Grieco, Takigawa, Bongers, Tanaka (b0160) 2005; 82 Chakraborty, Jayaprakash, Chakraborty, Jayaprakash, Laxman (b0060) 2001; 42 Mata, Thomas (b0190) 1995 Kunze, Jansen, Höfle, Reichenbach (b0005) 1994; 47 Babu, Li, Jacob, Zhang, Khan, Ferreira, Clark (b0150) 2006; 49 Sirasani, Paul, Andrade, Sirasani, Paul, Andrade, Andrade (b0090) 2008; 73 Sirasani (10.1016/j.tetlet.2012.02.049_b0100) 2010; 18 Feutrill (10.1016/j.tetlet.2012.02.049_b0045) 2002; 4 Kawai (10.1016/j.tetlet.2012.02.049_b0155) 2007; 63 Feutrill (10.1016/j.tetlet.2012.02.049_b0050) 2003; 56 Chakraborty (10.1016/j.tetlet.2012.02.049_b0070) 2001; 57 Crowley (10.1016/j.tetlet.2012.02.049_b0015) 2008; 16 Babu (10.1016/j.tetlet.2012.02.049_b0150) 2006; 49 Villa (10.1016/j.tetlet.2012.02.049_b0125) 2007; 9 Feutrill (10.1016/j.tetlet.2012.02.049_b0055) 2008; 64 Nakamura (10.1016/j.tetlet.2012.02.049_b0145) 2003; 5 Chakraborty (10.1016/j.tetlet.2012.02.049_b0065) 2001; 42 Andrade (10.1016/j.tetlet.2012.02.049_b0105) 2009; 41 Sirasani (10.1016/j.tetlet.2012.02.049_b0095) 2008; 73 Anderson (10.1016/j.tetlet.2012.02.049_b0165) 2005; 82 Feutrill (10.1016/j.tetlet.2012.02.049_b0040) 2000; 2 Beşev (10.1016/j.tetlet.2012.02.049_b0110) 2005; 70 Candy (10.1016/j.tetlet.2012.02.049_b0115) 2010; 75 Crowley (10.1016/j.tetlet.2012.02.049_b0185) 2007; Vol. 948 Crowley (10.1016/j.tetlet.2012.02.049_b0025) 2003; 57 Grieco (10.1016/j.tetlet.2012.02.049_b0170) 1980; 102 Kunze (10.1016/j.tetlet.2012.02.049_b0005) 1994; 47 Sewell (10.1016/j.tetlet.2012.02.049_b0140) 2011; 13 Pasqua (10.1016/j.tetlet.2012.02.049_b0135) 2011; 67 Nising (10.1016/j.tetlet.2012.02.049_b0030) 2011; 47 Mathieson (10.1016/j.tetlet.2012.02.049_b0130) 2009; 7 Dias (10.1016/j.tetlet.2012.02.049_b0085) 2005; 70 Mata (10.1016/j.tetlet.2012.02.049_b0190) 1995 Dias (10.1016/j.tetlet.2012.02.049_b0080) 2001; 3
References_xml	– volume: 42 start-page: 497 year: 2001 end-page: 499 ident: b0060 publication-title: Tetrahedron Lett. contributor: fullname: Laxman – volume: 63 start-page: 9049 year: 2007 end-page: 9056 ident: b0155 publication-title: Tetrahedron contributor: fullname: Uenishi – volume: 75 start-page: 1354 year: 2010 end-page: 1359 ident: b0115 publication-title: J. Org. Chem. contributor: fullname: Pons – volume: 9 start-page: 1631 year: 2007 end-page: 1633 ident: b0120 publication-title: Org. Lett. contributor: fullname: Marquez – volume: 49 start-page: 7877 year: 2006 end-page: 7886 ident: b0150 publication-title: J. Med. Chem. contributor: fullname: Clark – volume: 16 start-page: 10345 year: 2008 end-page: 10355 ident: b0010 publication-title: Bioorg. Med. Chem. contributor: fullname: Rodefeld – volume: 5 start-page: 3579 year: 2003 end-page: 3582 ident: b0145 publication-title: Org. Lett. contributor: fullname: Masaaki – ident: b0195 – volume: 70 start-page: 1696 year: 2005 end-page: 1708 ident: b0110 publication-title: Collect. Czech. Chem. Commun. contributor: fullname: Fürstner – volume: 47 start-page: 881 year: 1994 end-page: 886 ident: b0005 publication-title: J. Antibiot. contributor: fullname: Reichenbach – start-page: 785 year: 1995 end-page: 799 ident: b0190 publication-title: J. Chem. Soc., Perkin Trans. 1 contributor: fullname: Thomas – volume: 73 start-page: 6386 year: 2008 end-page: 6388 ident: b0090 publication-title: J. Org. Chem. contributor: fullname: Andrade – volume: 82 start-page: 134 year: 2005 end-page: 7588 ident: b0160 publication-title: Org. Synth. contributor: fullname: Tanaka – volume: 3 start-page: 3951 year: 2001 end-page: 3954 ident: b0075 publication-title: Org. Lett. contributor: fullname: Nigsch – volume: 2 start-page: 3365 year: 2000 end-page: 3367 ident: b0035 publication-title: Org. Lett. contributor: fullname: Rizzacasa – volume: 13 start-page: 800 year: 2011 ident: 10.1016/j.tetlet.2012.02.049_b0140 publication-title: Org. Lett. doi: 10.1021/ol103114w contributor: fullname: Sewell – volume: 102 start-page: 7587 year: 1980 ident: 10.1016/j.tetlet.2012.02.049_b0170 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00545a044 contributor: fullname: Grieco – volume: 9 start-page: 1631 year: 2007 ident: 10.1016/j.tetlet.2012.02.049_b0125 publication-title: Org. Lett. doi: 10.1021/ol070336e contributor: fullname: Villa – volume: 70 start-page: 1696 year: 2005 ident: 10.1016/j.tetlet.2012.02.049_b0110 publication-title: Collect. Czech. Chem. Commun. doi: 10.1135/cccc20051696 contributor: fullname: Beşev – volume: 3 start-page: 3951 year: 2001 ident: 10.1016/j.tetlet.2012.02.049_b0080 publication-title: Org. Lett. doi: 10.1021/ol016845c contributor: fullname: Dias – volume: 2 start-page: 3365 year: 2000 ident: 10.1016/j.tetlet.2012.02.049_b0040 publication-title: Org. Lett. doi: 10.1021/ol0064664 contributor: fullname: Feutrill – volume: 4 start-page: 525 year: 2002 ident: 10.1016/j.tetlet.2012.02.049_b0045 publication-title: Org. Lett. doi: 10.1021/ol017092x contributor: fullname: Feutrill – volume: 73 start-page: 6386 year: 2008 ident: 10.1016/j.tetlet.2012.02.049_b0095 publication-title: J. Org. Chem. doi: 10.1021/jo800906p contributor: fullname: Sirasani – volume: 56 start-page: 783 year: 2003 ident: 10.1016/j.tetlet.2012.02.049_b0050 publication-title: Aust. J. Chem. doi: 10.1071/CH03026 contributor: fullname: Feutrill – volume: 82 start-page: 134 year: 2005 ident: 10.1016/j.tetlet.2012.02.049_b0165 publication-title: Org. Synth. doi: 10.15227/orgsyn.082.0134 contributor: fullname: Anderson – volume: 42 start-page: 497 year: 2001 ident: 10.1016/j.tetlet.2012.02.049_b0065 publication-title: Tetrahedron Lett. doi: 10.1016/S0040-4039(00)02002-5 contributor: fullname: Chakraborty – volume: 5 start-page: 3579 year: 2003 ident: 10.1016/j.tetlet.2012.02.049_b0145 publication-title: Org. Lett. doi: 10.1021/ol035227o contributor: fullname: Nakamura – volume: 41 start-page: 359 year: 2009 ident: 10.1016/j.tetlet.2012.02.049_b0105 publication-title: Org. Prep. Proced. Int. doi: 10.1080/00304940903188084 contributor: fullname: Andrade – volume: 7 start-page: 2170 year: 2009 ident: 10.1016/j.tetlet.2012.02.049_b0130 publication-title: Org. Biomol. Chem. doi: 10.1039/b901797f contributor: fullname: Mathieson – volume: 18 start-page: 3648 year: 2010 ident: 10.1016/j.tetlet.2012.02.049_b0100 publication-title: Bioorg. Med. Chem. doi: 10.1016/j.bmc.2010.03.003 contributor: fullname: Sirasani – start-page: 785 year: 1995 ident: 10.1016/j.tetlet.2012.02.049_b0190 publication-title: J. Chem. Soc., Perkin Trans. 1 doi: 10.1039/p19950000785 contributor: fullname: Mata – volume: 16 start-page: 10345 year: 2008 ident: 10.1016/j.tetlet.2012.02.049_b0015 publication-title: Bioorg. Med. Chem. doi: 10.1016/j.bmc.2008.10.030 contributor: fullname: Crowley – volume: 70 start-page: 2225 year: 2005 ident: 10.1016/j.tetlet.2012.02.049_b0085 publication-title: J. Org. Chem. doi: 10.1021/jo047732k contributor: fullname: Dias – volume: 47 start-page: 4062 year: 2011 ident: 10.1016/j.tetlet.2012.02.049_b0030 publication-title: Chem. Commun. doi: 10.1039/c0cc05178k contributor: fullname: Nising – volume: 67 start-page: 7611 year: 2011 ident: 10.1016/j.tetlet.2012.02.049_b0135 publication-title: Tetrahedron doi: 10.1016/j.tet.2011.07.033 contributor: fullname: Pasqua – volume: 63 start-page: 9049 year: 2007 ident: 10.1016/j.tetlet.2012.02.049_b0155 publication-title: Tetrahedron doi: 10.1016/j.tet.2007.06.081 contributor: fullname: Kawai – volume: 49 start-page: 7877 year: 2006 ident: 10.1016/j.tetlet.2012.02.049_b0150 publication-title: J. Med. Chem. doi: 10.1021/jm061123i contributor: fullname: Babu – volume: 75 start-page: 1354 year: 2010 ident: 10.1016/j.tetlet.2012.02.049_b0115 publication-title: J. Org. Chem. doi: 10.1021/jo902582w contributor: fullname: Candy – volume: 57 start-page: 685 year: 2003 ident: 10.1016/j.tetlet.2012.02.049_b0025 publication-title: Chimia doi: 10.2533/000942903777678669 contributor: fullname: Crowley – volume: 57 start-page: 9461 year: 2001 ident: 10.1016/j.tetlet.2012.02.049_b0070 publication-title: Tetrahedron doi: 10.1016/S0040-4020(01)00940-1 contributor: fullname: Chakraborty – volume: 64 start-page: 4880 year: 2008 ident: 10.1016/j.tetlet.2012.02.049_b0055 publication-title: Tetrahedron doi: 10.1016/j.tet.2008.01.139 contributor: fullname: Feutrill – volume: 47 start-page: 881 year: 1994 ident: 10.1016/j.tetlet.2012.02.049_b0005 publication-title: J. Antibiot. doi: 10.7164/antibiotics.47.881 contributor: fullname: Kunze – volume: Vol. 948 year: 2007 ident: 10.1016/j.tetlet.2012.02.049_b0185 contributor: fullname: Crowley
SSID	ssj0000680
Score	2.114559
Snippet	The formal synthesis of (+)-crocacin C is reported. The approach described takes advantage of a highly regioselective epoxide cuprate addition and a...
SourceID	proquest crossref elsevier
SourceType	Aggregation Database Publisher
StartPage	2114
SubjectTerms	COPPER OXIDE Crocacins Cuprates FABRICATION Formal synthesis Overman rearrangement Synthesis (chemistry) Tetrahedrons
Title	Formal synthesis of (+)-crocacin C
URI	https://dx.doi.org/10.1016/j.tetlet.2012.02.049 https://search.proquest.com/docview/1744682453
Volume	53
hasFullText	1
inHoldings	1
isFullTextHit
isPrint
link	http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Zi9RAEG7c3Qd9EU9cL6IoKEMPk3Snj8d1Nsu6oAg7wr41nT4e1mGicyD4661Op5N44QFCCDMdkkmqaqq_qnxVjdAzZ33BS2OxL2qGKSMa10x7LIQE_Gx17dv1U07P-dsLcVzRakjmDGP_VdMwBroOlbN_oe3-ojAAn0HnsAetw_6P9H4SQOgydCIAaNd1GwEU-bx4BUE_BrdrtAmVfmNUunBb8DnOrsEUlm19T4-03-nNp13MvYYlcybVdJSBDoF2Qr8fJsf9oflaf06k-ZaGOznrj73Ra5iKvkRWt22WvhknHgKDg-LOV7bZsFQRM9CPWg9LZxCTxgZFUxedquAEhz5rY68bWwQn6_rWh8ay0m4-hq_sp74-ph0up1sHkgq02JDWhY3KYW7rGYfn4cbCfeWBlSJKvocOCvBN4BoPjl5XF2ej6VvMEtUynJDqLVtS4I-_9Ss8893M3sKVxQ10vYszsqNoIDfRFbe6ha7O0_J-t9HTaChZbyhZ47MXk5e9iWTzO-j9SbWYn-JuwQxsCJFbLJxlPq8JJVYaCrGABfioCQdYqGktLK9FTkzug1eXjtYstyUnjNvauJnjNbmL9lfNyt1DGYiJayFLaQBRhzpbz-HvXjIjDQTAnhwinB5bfYx9UVQiDF6qKCYVxKRmsFF5iHiSjeqwXcRsCtT5mzOfJFEqEFF4n6VXrtltFATTlImCluT-P1_9Abo22PZDtL9d79wjtLexu8edYXwFn8h4JA
link.rule.ids	315,782,786,27933,27934
linkProvider	Elsevier
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=Formal+synthesis+of+%28%2B%29-crocacin+C&rft.jtitle=Tetrahedron+letters&rft.au=Pasqua%2C+Adele+E.&rft.au=Ferrari%2C+Frank+D.&rft.au=Crawford%2C+James+J.&rft.au=Marquez%2C+Rodolfo&rft.date=2012-04-18&rft.pub=Elsevier+Ltd&rft.issn=0040-4039&rft.eissn=1873-3581&rft.volume=53&rft.issue=16&rft.spage=2114&rft.epage=2116&rft_id=info:doi/10.1016%2Fj.tetlet.2012.02.049&rft.externalDocID=S0040403912002857
thumbnail_l	http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0040-4039&client=summon
thumbnail_m	http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0040-4039&client=summon
thumbnail_s	http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0040-4039&client=summon