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- Enantioselective synthesis of α-halo-α-alkylmalonates via phase-transfer catalytic α-alkylation. Suckchang Hong, Minsik Kim, Myunggi Jung, Min Woo Ha, Myungmo Lee, Yohan Park, Mi-hyun Kim, Taek-Soo Kim, Jihoon Lee, Hyeung-geun Park
, Org. Biomol. Chem.
, 2014
, 12
, 1510
- Multi-catalysis cascade reactions based on the methoxycarbonylketene platform: diversity-oriented synthesis of functionalized non-symmetrical malonates for agrochemicals and pharmaceuticals. Dhevalapally B. Ramachary, Chintalapudi Venkaiah, Y. Vijayendar Reddy, Mamillapalli Kishor
, Org. Biomol. Chem.
, 2009
, 7
, 2053
- The synthesis of α-([11C]methyl)phenylalanine and α-([11C]methyl)tyrosine from 11C-labelled malonic esters. Antony D. Gee, Bengt Långström
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 215
- Thermoneutral synthesis of spiro-1,4-cyclohexadienes by visible-light-driven dearomatization of benzylmalonates. Quan-Qing Zhao, Julia Rehbein, Oliver Reiser
, Green Chem.
, 2022
, 24
, 2772
- Nano-K2CO3: preparation, characterization and evaluation of reactive activities. Jun-Zhang Li, Shi-Ming Fan, Xuan-Fei Sun, Shouxin Liu
, RSC Adv.
, 2016
, 6
, 1865
- Synthesis of maculalactone A and derivatives for environmental fate tracking studies. Samuel L. Bader, Michael U. Luescher, Karl Gademann
, Org. Biomol. Chem.
, 2015
, 13
, 199
- Synthetic approaches and functionalizations of imidazo[1,2-a]pyrimidines: an overview of the decade. Richa Goel, Vijay Luxami, Kamaldeep Paul
, RSC Adv.
, 2015
, 5
, 81608
- Novel peptide isosteres that were designed to inhibit the binding of the HIV surface glycoprotein (gp120) to the T cell surface glycoprotein CD4. Michael G. B. Drew, Stephen Gorsuch, John Mann, Shimon Yoshida
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 1627
- 11. Studies on the Michael reaction. Part II. The nature of the condensation product from ethyl benzylmalonate and ethyl fumarate. J. A. Gardner, H. N. Rydon
, J. Chem. Soc.
, 1938
, 42
- Synthetic and mechanistic studies of metal-free transfer hydrogenations applying polarized olefins as hydrogen acceptors and amine borane adducts as hydrogen donors. Xianghua Yang, Thomas Fox, Heinz Berke
, Org. Biomol. Chem.
, 2012
, 10
, 852