Esa T. Jarvi
Massachusetts Institute of Technology(US)
Publications by Year
Research Areas
Fluorine in Organic Chemistry, Asymmetric Synthesis and Catalysis, HIV/AIDS drug development and treatment, Synthetic Organic Chemistry Methods, Carbohydrate Chemistry and Synthesis
Most-Cited Works
- → 2'-Deoxy-2'-methylenecytidine and 2'-deoxy-2',2'-difluorocytidine 5'-diphosphates: potent mechanism-based inhibitors of ribonucleotide reductase(1991)252 cited
- → Terminal difluoro olefin analogs of squalene are time-dependent inhibitors of squalene epoxidase(1992)137 cited
- → Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diol(1988)125 cited
- → 4',5'-Unsaturated-5'-fluoro adenosine nucleosides: potent mechanism-based inhibitors of S-adenosyl-L-homocysteine hydrolase(1989)98 cited
- → A new route to vinyl fluorides(1990)89 cited
- → A new method for the electrophilic fluorination of vinyl stannanes.(1993)84 cited
- → The synthesis of α,α-difluoroaldehydes and ketones via claisen rearrangements(1985)71 cited
- → Difluoromethyldiphenylphosphine oxide. A new reagent for conversion of carbonyl compounds to 1,1-difluoroolefins.(1990)64 cited
- → Inactivation of Ribonucleotide Reductase by (E)-2‘-Fluoromethylene-2‘-deoxycytidine 5‘-Diphosphate: A Paradigm for Nucleotide Mechanism-Based Inhibitors(1996)64 cited
- → 4'-5'-Unsaturated 5'-halogenated nucleosides. Mechanism-based and competitive inhibitors of S-adenosyl-L-homocysteine hydrolase(1991)57 cited