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- Squaramide-catalysed enantionselective Mannich reaction of imines bearing a heterocycle with malonates. Hai-Xiao He, Da-Ming Du
, RSC Adv.
, 2013
, 3
, 16349
- Simple chiral sulfonamide
primary amine catalysed highly enantioselective Michael addition of malonates to enones. Chunhua Luo, Yu Jin, Da-Ming Du
, Org. Biomol. Chem.
, 2012
, 10
, 4116
- A heterogeneous layered bifunctional catalyst for the integration of aerobic oxidation and asymmetric C–C bond formation. Hiroyuki Miyamura, Gerald C. Y. Choo, Tomohiro Yasukawa, Woo-Jin Yoo, Shu Kobayashi
, Chem. Commun.
, 2013
, 49
, 9917
- Synthesis and evaluation of guanidinyl pyrrolidines as bifunctional catalysts for enantioselective conjugate additions to cyclic enones. Sunil V. Pansare, Rajinikanth Lingampally
, Org. Biomol. Chem.
, 2009
, 7
, 319
- Borrowing hydrogen: iridium-catalysed reactions for the formation of C–C bonds from alcohols. Phillip. J. Black, Gerta Cami-Kobeci, Michael G. Edwards, Paul A. Slatford, Michael K. Whittlesey, Jonathan M. J. Williams
, Org. Biomol. Chem.
, 2006
, 4
, 116
- Aza-Knoevenagel-type condensation of secondary amides: direct access to N-monosubstituted β,β-difunctionalized enamines. Pei-Qiang Huang, Wei Ou, Jian-Liang Ye
, Org. Chem. Front.
, 2015
, 2
, 1094
- Highly enantioselective and recyclable organocatalytic Michael addition of malonates to α,β-unsaturated aldehydes in aqueous media. Subrata K. Ghosh, Kritanjali Dhungana, Allan D. Headley, Bukuo Ni
, Org. Biomol. Chem.
, 2012
, 10
, 8322
- Recent synthetic applications of α-amido sulfones as precursors of N-acylimino derivatives. Enrico Marcantoni, Alessandro Palmieri, Marino Petrini
, Org. Chem. Front.
, 2019
, 6
, 2142
- Asymmetric catalytic carbon–carbon coupling reactions via C–H bond activation. Lei Yang, Hanmin Huang
, Catal. Sci. Technol.
, 2012
, 2
, 1099
- Visible light promoted cross-dehydrogenative coupling: a decade update. Avik Kumar Bagdi, Matiur Rahman, Dhananjay Bhattacherjee, Grigory V. Zyryanov, Sumit Ghosh, Oleg N. Chupakhin, Alakananda Hajra
, Green Chem.
, 2020
, 22
, 6632