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Page 1
The alkaloids of the madangamine group.
Alkaloids Chem Biol. 2015;74:159-99. doi: 10.1016/bs.alkal.2014.10.001.
Alkaloids Chem Biol. 2015.
PMID: 25845061
Review.
Total synthesis of (+)-madangamine D.
Ballette R, Pérez M, Proto S, Amat M, Bosch J.
Ballette R, et al. Among authors: proto s.
Angew Chem Int Ed Engl. 2014 Jun 10;53(24):6202-5. doi: 10.1002/anie.201402263. Epub 2014 May 2.
Angew Chem Int Ed Engl. 2014.
PMID: 24798407
Free article.
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Access to Enantiopure Advanced Intermediates en Route to Madangamines.
Are C, Pérez M, Ballette R, Proto S, Caso F, Yayik N, Bosch J, Amat M.
Are C, et al. Among authors: proto s.
Chemistry. 2019 Dec 10;25(69):15929-15933. doi: 10.1002/chem.201904045. Epub 2019 Nov 12.
Chemistry. 2019.
PMID: 31584737
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First enantioselective synthesis of tetracyclic intermediates en route to madangamine D.
Amat M, Ballette R, Proto S, Pérez M, Bosch J.
Amat M, et al. Among authors: proto s.
Chem Commun (Camb). 2013 Apr 18;49(30):3149-51. doi: 10.1039/c3cc41104d. Epub 2013 Mar 11.
Chem Commun (Camb). 2013.
PMID: 23474469
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First enantioselective synthesis of the diazatricyclic core of madangamine alkaloids.
Amat M, Pérez M, Proto S, Gatti T, Bosch J.
Amat M, et al. Among authors: proto s.
Chemistry. 2010 Aug 16;16(31):9438-41. doi: 10.1002/chem.201000421.
Chemistry. 2010.
PMID: 20379978
No abstract available.
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Model studies on the synthesis of madangamine alkaloids. Assembly of the macrocyclic rings.
Proto S, Amat M, Pérez M, Ballette R, Romagnoli F, Mancinelli A, Bosch J.
Proto S, et al.
Org Lett. 2012 Aug 3;14(15):3916-9. doi: 10.1021/ol301672y. Epub 2012 Jul 25.
Org Lett. 2012.
PMID: 22830949
Free article.
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