Serveur d'exploration sur le LRGP

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Le cluster Cyclization - Rearrangement

Terms

7Cyclization
5Rearrangement
5Reaction conditions
8Reagent
3Silane
6Reactive
4Selectivity
4Enol

Associations

Freq.WeightAssociation
44Cyclization - Rearrangement
44Cyclization - Reaction conditions
33Reagent - Silane
33Reagent - Rearrangement
33Reactive - Rearrangement
33Reactive - Reagent
33Reaction conditions - Selectivity
33Reaction conditions - Rearrangement
33Reaction conditions - Reactive
33Enol - Reactive
33Cyclization - Selectivity
33Cyclization - Reagent
33Cyclization - Reactive

Documents par ordre de pertinence
000143 (2001) Brian R. Bear [États-Unis] ; Steven M. Sparks [États-Unis] ; Kenneth J. Shea [États-Unis]The Type 2 Intramolecular Diels–Alder Reaction: Synthesis and Chemistry of Bridgehead Alkenes
000236 (1989) Gerald L. Larson [États-Unis]Organosilicon survey 1986-the SiliconCarbon bond
000256 (1986) R. Karl Dieter [États-Unis]α-Oxo ketene dithioacetals and related compounds: versatile three-carbon synthons
000046 (2012) David Tilly [Australie, Niger, France] ; Jakob Magolan [États-Unis] ; Jacques Mortier [France]Directed Remote Aromatic Metalations: Mechanisms and Driving Forces
000045 (2012) Barry M. Trost [États-Unis] ; W. Michael Seganish ; Cheol K. Chung ; Dominique AmansTotal Synthesis of Laulimalide: Synthesis of the Northern and Southern Fragments
000122 (2005) Barry M. Trost [États-Unis] ; Gretchen M. SchroederPalladium‐Catalyzed Asymmetric Allylic Alkylation of Ketone Enolates
000234 (1989) Glenn D. Prestwich [États-Unis] ; Czesław Wawrze Czyk [États-Unis]Synthesis of allyl vinyl silanes. Preparation of 12-(dimethylsila)squalene
000051 (2012) Bouchra Belaissaoui [France] ; Yann Le Moullec [France] ; David Willson [États-Unis] ; Éric Favre (génie des procédés) [France]Hybrid membrane cryogenic process for post-combustion CO2 capture
000068 (2011) John J. Eisch [États-Unis] ; John N. Gitua [États-Unis] ; Kun YuVersatile Zirconium Reductants and Carbon–Carbon Coupling Agents Selectively Accessible from the 2:1 Molar Aggregate of n‐Butyllithium and Zirconium(IV) Salts
000111 (2007) Michael J. Truex ; Christian D. Johnson ; James R. Spencer ; T. Prabhakar Clement [États-Unis] ; Brian B. Looney [États-Unis]A deterministic approach to evaluate and implement monitored natural attenuation for chlorinated solvents
000144 (2001) H. A. M. Van Mullekom [États-Unis] ; J. A. J. M. Vekemans [Pays-Bas] ; E. E. Havinga [Pays-Bas] ; E. W. Meijer [Pays-Bas]Developments in the chemistry and band gap engineering of donor–acceptor substituted conjugated polymers
000150 (2000) Jakob Busch-Petersen [États-Unis] ; E. J Corey [États-Unis]Sterically shielded secondary N -tritylamines and N -tritylamide bases, readily available and useful synthetic reagents
000156 (1998) Lucjan Strekowski [États-Unis] ; Shou-Yuan Lin [États-Unis] ; Hyeran Lee [États-Unis] ; Zhi-Qin Zhang [États-Unis] ; J. Christian Mason [États-Unis]Synthesis of 4-perfluoroalkylquinolines
000184 (1995) Simonetta A. Fontana [États-Unis] ; Charles R. Davis [États-Unis] ; Charles R. Ya-Bo He [États-Unis] ; Donald J. Burton [États-Unis]The stereoselective preparation of cis and trans -1,2-difluoroethylene synthons
000217 (1992) Clayton H. Heathcock [États-Unis]The Enchanting Alkaloids of Yuzuriha
000223 (1990) Albert J. Valocchi [États-Unis]Use of temporal moment analysis to study reactive solute transport in aggregated porous media
000224 (1990) Robert P. Discordia [États-Unis] ; Christopher K. Murphy [États-Unis] ; Donald C. Dittmer [États-Unis]Telluride-mediated stereospecific conversion of racemic E -allylic alcohols to homochiral Z -allylic alcohols; transposition of primary and secondary allylic alcohols via glycidol derivatives
000266 (1985) Michael T. Crimmins [États-Unis] ; S. Wayne Mascarella [États-Unis] ; Lori D. Bredon [États-Unis]Intramolecular photocycloadditions: synthesis of stericallycongested substituted [4.5.5.5] Fenestranes. Models for the total synthesis of laurenene and silphinene

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