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- A synthetic route towards 3,4-disubstituted pyrrolidin-2-ones via a Michael addition and reductive ring closing strategy. Monali Dawange, Nikita Parekh, Avinash Kumbhar, Wim Dehaen, Radhika Kusurkar
, New J. Chem.
, 2017
, 41
, 3612
- β-Substituted γ-butyrolactams from mucochloric acid: synthesis of (±)-baclofen and other γ-aminobutyric acids and useful building blocks. Kallolmay Biswas, Rajesh Gholap, Padakanti Srinivas, Sachin Kanyal, Koushik Das Sarma
, RSC Adv.
, 2014
, 4
, 2538
- Photochemical reaction of α-alkyl-β-oxoamides. Competitive γ- and δ-hydrogen abstraction by excited ketone carbonyl groups. Tadashi Hasegawa, Yoshiaki Arata, Kouichi Mizuno, Kenji Masuda, Nobutoshi Yoshihara
, J. Chem. Soc., Perkin Trans. 1
, 1986
, 541
- Reactivity of cyclic sulfamidates towards sulfur-stabilised enolates. Stereocontrolled synthesis of functionalised lactams. John F. Bower, Suda Chakthong, Jakub Švenda, Andrew J. Williams, Ron M. Lawrence, Peter Szeto, Timothy Gallagher
, Org. Biomol. Chem.
, 2006
, 4
, 1868
- Photocyclization of NN-disubstituted benzoylacetamides and acetoacetamides. Tadashi Hasegawa, Hiromu Aoyama, Yoshimori Omote
, J. Chem. Soc., Perkin Trans. 1
, 1976
, 2054
- Biocatalytic amide bond formation. Max Lubberink, William Finnigan, Sabine L. Flitsch
, Green Chem.
, 2023
, 25
, 2958
- Michael, Michael–aldol and Michael–Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives. Steven V. Ley, Darren J. Dixon, Richard T. Guy, Félix Rodríguez, Tom D. Sheppard
, Org. Biomol. Chem.
, 2005
, 3
, 4095
- A convenient synthesis and cytotoxic evaluation of β-aryl-α-methylidene-γ-lactones and β-aryl-α-methylidene-γ-lactams. Anna Albrecht, Łukasz Albrecht, Marek Różalski, Urszula Krajewska, Anna Janecka, Kazimierz Studzian, Tomasz Janecki
, New J. Chem.
, 2010
, 34
, 750
- Synthesis of nitrogen heterocycles via α-aminoalkyl radicals generated from α-silyl secondary amines under visible light irradiation. Kazunari Nakajima, Mai Kitagawa, Yuya Ashida, Yoshihiro Miyake, Yoshiaki Nishibayashi
, Chem. Commun.
, 2014
, 50
, 8900
- Formula index
, J. Chem. Soc.
, 1928
, 3370