Gold catalysis: tandem reactions of diyne-diols and external nucleophiles as an easy access to tricyclic cage-like structures.
about
Towards a general diastereoselective route to oxabicyclo[3.2.1]octanes via a gold-catalysed cascade reactionGold catalysis in total synthesis--an update.Triptycene diols: a strategy for synthesizing planar π systems through catalytic conversion of a poly(p-phenylene ethynylene) into a poly(p-phenylene vinylene)Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity.Enantioselective, Stereodivergent Hydroazidation and Hydroamination of Allenes Catalyzed by Acyclic Diaminocarbene (ADC) Gold(I) Complexes.The tandem intermolecular hydroalkoxylation/Claisen rearrangement.Palladium-catalyzed aerobic intermolecular cyclization of acrylic acid with 1-octene to afford α-methylene-γ-butyrolactones: the remarkable effect of continuous water removal from the reaction mixture and analysis of the reaction by kinetic, ESI-MS,Stereoselective Gold(I)-Catalyzed Intermolecular Hydroalkoxlation of Alkynes.On the Gold-Catalyzed Generation of Vinyl Cations from 1,5-Diynes.Gold(I)-Catalyzed N-Desulfonylative Amination versus N-to-O 1,5-Sulfonyl Migration: A Versatile Approach to 1-Azabicycloalkanes.Cyclization Reactions of Aryl Propargyl Acetates with Tethered Epoxide Induced by Ruthenium Complex.Reductant-directed formation of PS-PAMAM-supported gold nanoparticles for use as highly active and recyclable catalysts for the aerobic oxidation of alcohols and the homocoupling of phenylboronic acids.Mutual Cooperation in the Formal Allyl Alcohol Nucleophilic Substitution and Hydration of Alkynes for the Construction of γ-Substituted Ketones.Aerobic oxidation of alcohols in the liquid phase with nanoporous gold catalysts
P2860
Q36251852-DFFB0662-3021-4513-8B92-0B3848FB7384Q37969890-9E969658-E210-4E56-8BC9-35154660E9DAQ41207393-1A5B1ECD-D0C0-49B9-9F14-29ADEC95494BQ41962217-C8AA4AA2-7ED7-4A07-83D8-E60B410B8939Q42415649-DB227D46-1531-4792-A149-D8118DBC99F7Q45114099-246E258A-D760-41E1-90DF-44279B57D89AQ46580486-69F3B6A8-09FB-4C5B-8986-B2442DF16A67Q47098587-47B22704-0859-4CB8-B0D9-FAEEABC3473EQ48047372-F05C3E06-9FD6-4E09-9D96-7E4DF9960D44Q48197672-64B1A147-BA36-427E-A65E-73F8C25574ABQ48239652-461E69E1-D9F0-4C1E-9F3D-9CF927235320Q49209269-E06EB1AB-F9EF-48C2-90C3-9A5A0F7A3FD3Q51466391-2E942FC3-F7F8-4CE6-A195-9631CB6193A9Q57726488-B91110F4-0A03-4B4E-BE94-7DCCD6EB14B7
P2860
Gold catalysis: tandem reactions of diyne-diols and external nucleophiles as an easy access to tricyclic cage-like structures.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Gold catalysis: tandem reactio ...... ricyclic cage-like structures.
@en
Gold catalysis: tandem reactio ...... ricyclic cage-like structures.
@nl
type
label
Gold catalysis: tandem reactio ...... ricyclic cage-like structures.
@en
Gold catalysis: tandem reactio ...... ricyclic cage-like structures.
@nl
prefLabel
Gold catalysis: tandem reactio ...... ricyclic cage-like structures.
@en
Gold catalysis: tandem reactio ...... ricyclic cage-like structures.
@nl
P2093
P356
P1476
Gold catalysis: tandem reactio ...... ricyclic cage-like structures.
@en
P2093
A Stephen K Hashmi
Marcel Wieteck
Matthias Rudolph
Michael Wölfle
Miriam Bührle
Wolfgang Frey
P304
P356
10.1002/CHEM.201001322
P407
P577
2010-08-01T00:00:00Z