A general enantioselective route to the chamigrene natural product family. - Wikidata - awgldk - TriplyDB

A general enantioselective route to the chamigrene natural product family.

A general enantioselective route to the chamigrene natural product family.

http://www.wikidata.org/entity/Q41788466

about

The Construction of All-Carbon Quaternary Stereocenters by Use of Pd-Catalyzed Asymmetric Allylic Alkylation Reactions in Total Synthesis Formal total syntheses of classic natural product target molecules via palladium-catalyzed enantioselective alkylation.Transition metal-catalyzed decarboxylative allylation and benzylation reactions Total syntheses of natural products containing spirocarbocycles.Advances in Stereoconvergent Catalysis from 2005 to 2015: Transition-Metal-Mediated Stereoablative Reactions, Dynamic Kinetic Resolutions, and Dynamic Kinetic Asymmetric Transformations.Palladium-Catalyzed Asymmetric Alkylation in the Synthesis of Cyclopentanoid and Cycloheptanoid Core Structures Bearing All-Carbon Quaternary Stereocenters.Effect of elatol, isolated from red seaweed Laurencia dendroidea, on Leishmania amazonensis.The catalytic enantioselective total synthesis of (+)-liphagal.Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies.The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation.Well-defined silica supported bipodal molybdenum oxo alkyl complexes: a model of the active sites of industrial olefin metathesis catalysts.

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P2860

A general enantioselective route to the chamigrene natural product family.

http://www.wikidata.org/entity/Q41788466

description

2010 nî lūn-bûn

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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2010年论文

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2010年论文

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name

A general enantioselective route to the chamigrene natural product family.

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A general enantioselective route to the chamigrene natural product family.

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A general enantioselective route to the chamigrene natural product family.

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J.TET.2010.04.128

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A general enantioselective route to the chamigrene natural product family.

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Brian M Stoltz

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David E White

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Ian C Stewart

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Robert H Grubbs

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P2860

Brominations of steroidal hormone having alpha,beta-unsaturated ketone, 17-O-acetyltestosterone, in the presence of silver triflate.

A facile and modular synthesis of phosphinooxazoline ligands.

Enantioselective synthesis of (+)-majusculone.

Construction of bridged and fused ring systems via intramolecular Michael reactions of vinylnitroso compounds.

Conformations of N-heterocyclic carbene ligands in ruthenium complexes relevant to olefin metathesis.

Unusual allylpalladium carboxylate complexes: identification of the resting state of catalytic enantioselective decarboxylative allylic alkylation reactions of ketones.

Catalytic enantioselective approach to the eudesmane sesquiterpenoids: total synthesis of (+)-carissone.

The first examples of ring-closing olefin metathesis of vinyl chlorides.

The catalytic asymmetric total synthesis of elatol.

Enantioselective total synthesis of (+)-cassiol.

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4668-4686

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10.1016/J.TET.2010.04.128

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26

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66

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Brinton Seashore-Ludlow

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46010118

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20798895

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enantioselectivity

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2925317

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