Christina Moberg, Ph.D.

Organic Chemistry KTH Royal Institute of Technology, Stockholm, Stockholms län, Sweden 
Organic Chemistry
"Christina Moberg"
Mean distance: 8.24
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Pàmies O, Margalef J, Cañellas S, et al. (2021) Recent Advances in Enantioselective Pd-Catalyzed Allylic Substitution: From Design to Applications. Chemical Reviews
Moberg C. (2016) Recycling in Asymmetric Catalysis. Accounts of Chemical Research. 49: 2736-2745
Xiao YC, Moberg C. (2016) Silaborative Carbocyclizations of 1,7-Enynes. Diastereoselective Preparation of Chromane Derivatives. Organic Letters
Moberg C. (2016) Minor enantiomer recycling – a strategy to improve enantioselectivity Pure and Applied Chemistry. 88: 309-316
Hertzberg R, Dinér P, Moberg C. (2016) Palladium-Catalyzed C(sp3)–C(sp2) Cross-Couplings of O-(α-Bromoacyl) Cyanohydrins with Boronic Acids: An Entry to Enantio­enriched N-Acylated β-Amino Alcohols Synthesis. 48: 3175-3182
Li E, Zhou H, Östlund V, et al. (2016) Regio- and stereoselective synthesis of conjugated trienes from silaborated 1,3-enynes New Journal of Chemistry. 40: 6340-6346
Bellini R, Magre M, Biosca M, et al. (2016) Conformational Preferences of a Tropos Biphenyl Phosphinooxazoline-a Ligand with Wide Substrate Scope Acs Catalysis. 6: 1701-1712
Théveau L, Bellini R, Dydio P, et al. (2016) Cofactor-Controlled Chirality of Tropoisomeric Ligand Organometallics. 35: 1956-1963
Laurell Nash A, Hertzberg R, Wen YQ, et al. (2015) Dual Lewis Acid-Lewis Base Catalyzed Acylcyanation of Aldehydes: A Mechanistic Study. Chemistry (Weinheim An Der Bergstrasse, Germany)
Hertzberg R, Monreal Santiago G, Moberg C. (2015) Synthesis of the β3-adrenergic receptor agonist solabegron and analogous N-(2-ethylamino)-β-amino alcohols from O-acylated cyanohydrins - expanding the scope of minor enantiomer recycling. The Journal of Organic Chemistry. 80: 2937-41
See more...