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- Facile synthesis of structurally diverse 5-oxopiperazine-2-carboxylates as dipeptide mimics and templates. Michael Limbach, Alexander V. Lygin, Vadim S. Korotkov, Mazen Es-Sayed, Armin de Meijere
, Org. Biomol. Chem.
, 2009
, 7
, 3338
- High yielding selective access to spirocyclopropanated 5-oxopiperazine-2-carboxylates and 1,4-diazepane-2,5-diones from methyl 2-chloro-2-cyclopropylideneacetate. Michael Limbach, Vadim S. Korotkov, Mazen Es-Sayed, Armin de Meijere
, Org. Biomol. Chem.
, 2008
, 6
, 3816
- [4 + 2] Cycloaddition of thiophene S-monoxides to activated methylenecyclopropanes. Thies Thiemann, Daisuke Ohira, Yuanqiang Li, Tsuyoshi Sawada, Shuntaro Mataka, Karsten Rauch, Mathias Noltemeyer, Armin de Meijere
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 2968
- A new cascade ring enlargement of isoxazolidines formed from 2-chloro-2-cyclopropylideneacetates. Chiara Zorn, Andrea Goti, Alberto Brandi, Andrea Goti, Keyji Johnsen, Sergei I. Kozhushkov, Armin de Meijere
, Chem. Commun.
, 1998
, 903
- Haloalkenes activated by geminal groups in reactions with N-nucleophiles. Aleksandr Y. Rulev
, Russ. Chem. Rev.
, 1998
, 67
, 279
- Construction of polysubstituted spiro[2.3] or [3.3] cyclic frameworks fused with a tosylated pyrrolidine promoted by visible-light-induced photosensitization. Xintao Gu, Yin Wei, Min Shi
, Org. Chem. Front.
, 2021
, 8
, 6823
- Tandem transformations initiated and determined by the Michael reaction. Elena V. Gorobets, Mansur S. Miftakhov, Farid A. Valeev
, Russ. Chem. Rev.
, 2000
, 69
, 1001
- New short syntheses of isoquinoline-4-carboxylic acid and 2-aza-3,3a-dihydroazulene-3a-carboxylic acid derivatives. Ludger Wessjohann, Lars Skattebøl, Armin De Meijere
, J. Chem. Soc., Chem. Commun.
, 1990
, 574