601 results on '"Prandi, Cristina"'
Search Results
202. LICKOR Promoted Formation of Conjugated Dienes as Useful Building Blocks for Palladium-Catalyzed Syntheses.
203. New Synthetic Approach to Cyclopenta-Fused Heterocycles Based upon a Mild Nazarov Reaction. Part 2. Further Studies on the Torquoselectivity.
204. A New Practical Synthesis of Germylalkoxydienes, Acylgermanes and Ethynylgermanes from α,β-Unsaturated and α-Phenyl Acetals
205. Synthesis and characterisation of estrogenic carriers for cytotoxic Pt(ii) fragments: biological activity of the resulting complexes
206. New Synthetic Approach to Cyclopenta‐Fused Heterocycles Based upon a Mild Nazarov Reaction.
207. Palladium‐Catalyzed Heck Reaction on 1‐Alkoxy‐1,3‐dienes: A Regioselective γ‐Arylation of α,β‐Unsaturated Carbonyl Compounds.
208. Palladium-Catalyzed C—C Bond Formation: Synthesis of 1,1-Dialkylbuta-1,3-dienes and β-Phenylstyrenes via Organoboron Intermediates.
209. α,β‐Unsaturated Acetals in Synthesis
210. Palladium-Catalyzed Heck Reaction on 1-Alkoxy-1,3-dienes: A Regioselective γ-Arylation of α,β-Unsaturated Carbonyl Compounds
211. Palladium-Catalyzed C−C Bond Formation: Synthesis of 1,1-Dialkylbuta-1,3-dienes and β-Phenylstyrenes via Organoboron Intermediates
212. Synthesis of α-Acyl-Functionalized Azacycles by Pd-Catalyzed Cross-Coupling Reactions of α-Alkoxyboronates with Lactam-Derived Vinyl Triflates
213. Uniformly sized molecularly imprinted polymers (MIPs) for 17β-estradiol
214. ChemInform Abstract: Lithium—Potassium Superbases as Key Reagents for the Base‐Catalyzed Isomerization of Some Terpenoids.
215. A New Synthesis of Butadienyl- and Styrylboronic Esters: Highly Reactive Intermediates for Suzuki Cross-Coupling
216. ChemInform Abstract: A New Palladium‐Catalyzed Synthesis of 1,1‐Dialkylbuta‐1,3‐dienes via Organoboron Intermediates.
217. Lithium–potassium superbases as key reagents for the base-catalysed isomerisation of some terpenoids
218. ChemInform Abstract: LIC‐KOR‐Promoted Access to a Tetrahydroindanone Precursor.
219. ChemInform Abstract: Alkoxydienylstannanes via Metalation of α,β‐Unsaturated and α‐Phenyl Acetals: Preparation and Synthetic Uses in the Stille Cross‐Coupling Reaction.
220. ChemInform Abstract: Preparation of Acetal- and Carbonyl-Substituted Allyl Chlorides from α,β-Unsaturated Acetals.
221. LIC-KOR-PROMOTED ACCESS TO A TETRAHYDROINDANONE PRECURSOR
222. Alkoxydienylstannanes via metalation of α,β-unsaturated and α-phenyl acetals: preparation and synthetic uses in the Stille cross-coupling reaction
223. A new palladium-catalysed synthesis of 1,1-dialkylbuta-1,3-dienes via organoboron intermediates
224. Preparation of Acetal- and Carbonyl-Substituted Allyl Chlorides from α,β-Unsaturated Acetals
225. A Short and Efficient New Synthesis of γ-Halo-Substituted α,β-Unsaturated Acetals and Carbonyl Compounds
226. Mixed Superbase LICKOR as a Key Reagent for the Synthesis of Conjugate Dienes from Citral and Farnesal – A New Route to a Potential Mimic Agent of Juvenile Hormones by Diels–Alder Cycloaddition
227. ChemInform Abstract: Mixed Metal Base LICKOR as Key Reagent in the Synthesis of Conjugate Alkadien‐1‐ols. A New Route to an Insect Attractant.
228. Mixed metal base LICKOR as key reagent in the synthesis of conjugate alkadien-1-ols. A new route to an insect attractant
229. Synthesis of 5-Oxatrienes: Useful Intermediates for the Preparation of Hexahydrobenzofuran Structures by Intramolecular Diels-Alder Reaction
230. Intramolecular Diels–Alder reaction of functionalized trienes: synthesis of medium-ring lactones †
231. Titanium dioxide - photocatalysed degradation of some anilides
232. Titanium dioxide-photocatalysed decomposition of some thiocarbamates in water
233. Synthesis of Functionalized Trienes and Regioselective Formation of Medium-Ring Lactones through Intramolecular Diels−Alder Reaction
234. Reaction of α,β-unsaturated and α-phenyl acetals with epoxides, promoted by lithium. Potassium mixed base LICKOR: Synthesis of homoallyl alcohols
235. LICKOR-Promoted 1,2-elimination in 1,1-dimethoxy-2-phenylethane and 1,1-dimethoxy-2-phenylpropane: synthesis of substituted enol ethers and alkynes
236. 1,1-Diethoxybut-2-ene as a Precursor of (2-Hydroxyethyl)-Substituted Alkoxy Dienes: Convenient Intermediates for a New Synthesis of 2-Substituted and 2,6-Disubstituted Tetrahydro-4H-pyran-4-ones
237. Addition reaction of gem-dichloroallyl lithium to benzophenones in the presence of macrocyclic ligands: formation of chloro oxiranes
238. 1-Substituted 1-ethoxy dienes obtained by reaction of 1,1-diethoxybut-2-ene with electrophiles in the presence of the mixed metal base LICKOR
239. Synthesis of Both Enantiomers of the Streptomyces Alkaloid 4-ep/-SS20846A.
240. Alkylation of enol ethers obtained by treatment of α,β-unsaturated acetals with organopotassium reagents: an inverse polarity approach
241. A New, Practical and Efficient Method for Protecting Alcohols as tert-Butyl Ethers.
242. Palladium-catalysed Heck reaction on 1,2-dien-1-ols: a stereoselective synthesis of α-arylated α,β-unsaturated aldehydes
243. Synthesis of Weinreb Amides via Pd-Catalyzed Aminocarbonylation of Heterocyclic-Derived Triflates.
244. Heck Reaction on 1-Alkoxy-1,3-dienes in Ionic Liquids: A Superior Medium for the Regioselective Arylation of the Conjugated Dienic System.
245. Remote Stereocontrol in the Nazarov Reaction: A New Approach to the Core of Roseophilin.
246. New Synthetic Approach to Cyclopenta-Fused Heterocycles Based upon a Mild Nazarov Reaction. 2. Further Studies on the Torquoselectivity.
247. New Synthetic Approach to Cyclopenta-Fused Heterocycles Based upon a Mild Nazarov Reaction.
248. Microwave-Assisted, One-Pot Synthesis of Doxycycline under Heterogeneous Catalysis in Water.
249. Strigolactones, from Plants to Human Health: Achievements and Challenges.
250. 4‐Methyltetrahydropyran: A Versatile Alternative Solvent for the Preparation of Chiral BINOL Catalysts and the Asymmetric Alkylation of Aldehydes.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.