Zeynep Dilşad Susam

E-mail

dsusam@metu.edu.tr

Department

ORCID

0000-0001-5404-5296

Scopus Author ID

57194765336

Web of Science Researcher ID

ABA-2687-2020

Organocatalytic enantioselective synthesis of dihydronaphthofurans and dihydrobenzofurans: reaction development and insights into stereoselectivity Susam, Zeynep Dilşad; Ozcan, Bilge Deniz; Kurtkaya, Enis; Yıldırım, Erol; Tanyeli, Cihangir (2022-10-01) Squaramide/cinchona alkaloid-derived bifunctional organocatalysts are in high demand in asymmetric transformations. Bifunctional quinine-derived sterically encumbered squaramide (H-bond donor) organocatalysts were used to ...
Enantioselective synthesis of 2,3-dihydrofurans using a bifunctional quinine/squaramide organocatalyst Susam, Zeynep Dilşad; Gundogdu, Gulsum; Tanyeli, Cihangir (2021-11-01) Asymmetric organocatalytic domino type Michael-S(N)2 reactions give access to enantiomerically enriched dihydrofuran derivatives that can be used as valuable chiral building blocks. A variety of alpha-bromonitroalkenes and...
Bifonksiyonel Skuaramit Organokatalizörlerin Friedel/Crafts Domino Tipi Tepkimelerde İncelenmesi Susam, Zeynep Dilşad; Tanyeli, Cihangir (2017-09-14)
Enantioselective aza-Henry reaction of t-Boc protected imines and nitroalkanes with bifunctional squaramide organocatalysts Susam, Zeynep Dilşad; Tanyeli, Cihangir (2017-05-07) An organocatalytic asymmetric aza-Henry reaction of t-Boc protected imines with nitroalkanes has been established by chiral acid-base type bifunctional Cinchona alkaloid/squaramide organocatalysts. The cooperation of a qui...
Enantioselective aza-Henry reaction of t-Boc protected imines and nitroalkanes with bifunctional squaramide organocatalysts Susam, Zeynep Dilşad; Tanyeli, Cihangir (2016-08-25)
Evaluation of bifunctional organocatalysts in Friedel Crafts substitution domino type reaction Susam, Zeynep Dilşad; Tanyeli, Cihangir (2016-08-25)
Nitroalkanların t Boc Korunumlu İminlerle Organokatalik Enantiyoseçici Aza Henry Tepkimesi Susam, Zeynep Dilşad; Tanyeli, Cihangir (null; 2015-03-22)

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