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MAELYS AMAT, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1285128918IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
276096(MA)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
OTHER
Class of 2018
Research & Publications (20)
Enantioselective total synthesis of the indole alkaloid 16-episilicine.
PMID 19436915·Chem Commun (Camb)·2009
8-other
A general synthetic route to enantiopure 5-substituted cis-decahydroquinolines.
PMID 19118477·J Org Chem·2009
8-other
Enantioselective formal synthesis of (+)-dihydrocorynantheine and (-)-dihydrocorynantheol.
PMID 19072689·J Org Chem·2009
8-other
Coarse molecular-dynamics analysis of an order-to-disorder transformation of a krypton monolayer on graphite.
PMID 19045385·J Chem Phys·2008
8-other
An enantioselective synthetic route to cis-2,4-disubstituted and 2,4-bridged piperidines.
PMID 18666797·J Org Chem·2008
8-other
A biomimetic enantioselective approach to the decahydroquinoline class of dendrobatid alkaloids.
PMID 18383489·Angew Chem Int Ed Engl·2008
7-preclinical
Animal behavior case of the month. Two cats were evaluated because of aggression towards each other and their owners.
PMID 17764428·J Am Vet Med Assoc·2007
5-case
Enantioselective spirocyclizations from tryptophanol-derived oxazolopiperidone lactams.
PMID 17602493·Org Lett·2007
8-other
Straightforward methodology for the enantioselective synthesis of benzo[a]- and indolo[2,3-a]quinolizidines.
PMID 17547461·J Org Chem·2007
8-other
Enantioselective synthesis of 3,3-disubstituted piperidine derivatives by enolate dialkylation of phenylglycinol-derived oxazolopiperidone lactams.
PMID 17488127·J Org Chem·2007
8-other
Dynamic kinetic resolution and desymmetrization processes: a straightforward methodology for the enantioselective synthesis of piperidines.
PMID 16850515·Chemistry·2006
8-other
Alkylation of phenylglycinol-derived oxazolopiperidone lactams. Enantioselective synthesis of beta-substituted piperidines.
PMID 16674053·J Org Chem·2006
8-other
Highly enantioselective dynamic kinetic resolution and desymmetrization processes by cyclocondensation of chiral aminoalcohols with racemic or prochiral delta-oxoacid derivatives.
PMID 15742067·Chem Commun (Camb)·2005
8-other
Conjugate additions to phenylglycinol-derived unsaturated delta-lactams. Enantioselective synthesis of uleine alkaloids.
PMID 15575744·J Org Chem·2004
8-other
Enantioselective formal synthesis of uleine alkaloids from phenylglycinol-derived bicyclic lactams.
PMID 15263938·Chem Commun (Camb)·2004
8-other
Enantioselective synthesis of cis- and trans-3,5-disubstituted piperidines. Synthesis of 20S- and 20R-dihydrocleavamine.
PMID 12917001·Org Lett·2003
8-other
Enantioselective synthesis of piperidine, indolizidine, and quinolizidine alkaloids from a phenylglycinol-derived delta-lactam.
PMID 12608811·J Org Chem·2003
8-other
Dynamic kinetic resolution and desymmetrization of enantiotopic groups by cyclodehydration of racemic or prochiral delta-oxoesters with (R)-phenylglycinol: enantioselective synthesis of piperidines.
PMID 12491424·Angew Chem Int Ed Engl·2002
8-other
Stereodivergent synthesis of enantiopure cis- and trans-3-Ethyl-4-piperidineacetates.
PMID 12153235·Org Lett·2002
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 330 BROOKLINE AVE
BOSTON, MA 02215 - Phone
- (617) 667-7000
Quick Facts
- NPI
- 1285128918
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 8
- Publications
- 20
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