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- Formal [4+1] cyclization of (thio/imido)hydrazides and ethyl 3,3,3-trifluoropropanoate: unified synthesis of 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles. Lan Zhao, Jun Xu, Jun Ma, Guangwei Yin, Fangyi Li, Tongchuan Suo, Chunhua Wang
, New J. Chem.
, 2022
, 46
, 20755
- Synthesis and SARs of indole-based α-amino acids as potent HIV-1 non-nucleoside reverse transcriptase inhibitors. Xin Han, Haoming Wu, Wei Wang, Chune Dong, Po Tien, Shuwen Wu, Hai-Bing Zhou
, Org. Biomol. Chem.
, 2014
, 12
, 8308
- Accurate determinations of the extent to which the SE2′ reactions of allyl-, allenyl- and propargylsilanes are stereospecifically anti. Michael J. C. Buckle, Ian Fleming, Salvador Gil, Kah Ling Christine Pang
, Org. Biomol. Chem.
, 2004
, 2
, 749
- Synthesis of mono-fluorinated heterocycles with a ring-junction nitrogen atom via Rh(iii)-catalyzed CF3-carbenoid C–H functionalization and defluorinative annulation. Haosheng Li, Mingjing Mei, Duozhi Wang, Lei Zhou
, Org. Chem. Front.
, 2023
, 10
, 1544
- Rhodium(iii)-catalyzed CF3-carbenoid C–H functionalization of 6-arylpurines. Daria V. Vorobyeva, Mikhail M. Vinogradov, Yulia V. Nelyubina, Dmitry A. Loginov, Alexander S. Peregudov, Sergey N. Osipov
, Org. Biomol. Chem.
, 2018
, 16
, 2966
- The photochemical Wolff rearrangement of 3-diazo-1,1,1-trifluoro-2-oxopropane revisited. Peter Haiss, Klaus-Peter Zeller
, Org. Biomol. Chem.
, 2003
, 1
, 2556
- Methyltrifluoropyruvate
imines possessing N-oxalyl and N-phosphonoformyl groups—precursors to a variety of α-CF3-α-amino acid derivatives. Hanna Skarpos, Daria V. Vorob'eva, Sergey N. Osipov, Irina L. Odinets, Eli Breuer, Gerd-Volker Röschenthaler
, Org. Biomol. Chem.
, 2006
, 4
, 3669
- Stereocontrol of 1,5-related stereocentres using an intermediate silyl group—the diastereoselectivity of nucleophilic attack on a double bond adjacent to a stereogenic centre carrying a silyl group. Ian Fleming, Pranab Maiti, Chandrashekar Ramarao
, Org. Biomol. Chem.
, 2003
, 1
, 3989
- Ligand-free copper-catalyzed borylative defluorination: access to gem-difluoroallyl boronic acid derivatives. Ashley M. Gates, Swetha Jos, Webster L. Santos
, Org. Biomol. Chem.
, 2022
, 20
, 366
- Multiple-fold C–F bond functionalization for the synthesis of (hetero)cyclic compounds: fluorine as a detachable chemical handle. Danhua Ge, Xue-Qiang Chu
, Org. Chem. Front.
, 2022
, 9
, 2013