Regioselective convergent synthesis of 2-arylidene thiazolo[3,2-]pyrimidines as potential anti-chikungunya agents
Convergent and convenient regioselective synthesis of novel thiazolo[2,3- a ]pyrimidine derivatives was accomplished using the one-pot reaction of 6-ethylthiouracil, bromoacetic acid, anhydrous sodium acetate, acetic anhydride, acetic acid and suitable aldehyde. X-ray crystallographic study reveals...
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creator | Fares, Mohamed McCosker, Patrick M Alsherbiny, Muhammad A Willis, Anthony C Clark, Timothy Neyts, Johan Jochmans, Dirk Keller, Paul A |
description | Convergent and convenient regioselective synthesis of novel thiazolo[2,3-
a
]pyrimidine derivatives was accomplished using the one-pot reaction of 6-ethylthiouracil, bromoacetic acid, anhydrous sodium acetate, acetic anhydride, acetic acid and suitable aldehyde. X-ray crystallographic study reveals the presence of the
Z
configuration of only one regioisomer confirmed by computational studies as being the most likely isomer present.
Convergent and convenient regioselective synthesis of novel thiazolo[2,3-
a
]pyrimidines was accomplished using the one-pot reaction of 6-ethylthiouracil, bromoacetic acid, anhydrous sodium acetate, acetic anhydride, acetic acid and suitable aldehyde. |
doi_str_mv | 10.1039/d0ra00257g |
format | Article |
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Z
configuration of only one regioisomer confirmed by computational studies as being the most likely isomer present.
Convergent and convenient regioselective synthesis of novel thiazolo[2,3-
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a
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Z
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Convergent and convenient regioselective synthesis of novel thiazolo[2,3-
a
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a
]pyrimidine derivatives was accomplished using the one-pot reaction of 6-ethylthiouracil, bromoacetic acid, anhydrous sodium acetate, acetic anhydride, acetic acid and suitable aldehyde. X-ray crystallographic study reveals the presence of the
Z
configuration of only one regioisomer confirmed by computational studies as being the most likely isomer present.
Convergent and convenient regioselective synthesis of novel thiazolo[2,3-
a
]pyrimidines was accomplished using the one-pot reaction of 6-ethylthiouracil, bromoacetic acid, anhydrous sodium acetate, acetic anhydride, acetic acid and suitable aldehyde.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>35498334</pmid><doi>10.1039/d0ra00257g</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-0007-263X</orcidid><orcidid>https://orcid.org/0000-0001-9337-2441</orcidid><orcidid>https://orcid.org/0000-0002-9265-6028</orcidid><orcidid>https://orcid.org/0000-0003-0589-3955</orcidid><orcidid>https://orcid.org/0000-0001-7931-4659</orcidid><orcidid>https://orcid.org/0000-0003-4868-845X</orcidid><orcidid>https://orcid.org/0000-0002-0033-7514</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetic acid Aldehydes Chemistry Chikungunya virus Convergence Crystallography Pyrimidines Regioselectivity Sodium acetate Synthesis |
title | Regioselective convergent synthesis of 2-arylidene thiazolo[3,2-]pyrimidines as potential anti-chikungunya agents |
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