Prins-type macrocyclizations as an efficient ring-closing strategy in natural product synthesis.
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Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural ProductCapturing Biological Activity in Natural Product Fragments by Chemical SynthesisDesigned, synthetically accessible bryostatin analogues potently induce activation of latent HIV reservoirs in vitroFeCl3-Catalyzed Tandem Prins and Friedel-Crafts Cyclization: A Highly Diastereoselective Route to Polycyclic Ring Structures.Total synthesis of bryostatin 9Silyl enol ether Prins cyclization: diastereoselective formation of substituted tetrahydropyran-4-onesTranslating Nature's Library: The Bryostatins and Function-Oriented SynthesisAssembly of four diverse heterocyclic libraries enabled by Prins cyclization, Au-catalyzed enyne cycloisomerization, and automated amide synthesis.Highly stereoselective Brønsted acid catalyzed synthesis of spirooxindole pyrans.Total synthesis of the cyanolide A aglycon.Lead Diversification through a Prins-Driven Macrocyclization Strategy: Application to C13-Diversified Bryostatin Analogues.Cu(II)-catalyzed olefin migration and Prins cyclization: highly diastereoselective synthesis of substituted tetrahydropyrans.Pyranone natural products as inspirations for catalytic reaction discovery and developmentAdvances in the synthesis of glycosidic macrolides: clavosolides A-D and cyanolide A.Synthesis of bridged inside-outside bicyclic ethers through oxidative transannular cyclization reactions.Mechanistic and computational studies of exocyclic stereocontrol in the synthesis of bryostatin-like cis-2,6-disubstituted 4-alkylidenetetrahydropyrans by Prins cyclization.Toward the Ideal Synthesis and Transformative Therapies: The Roles of Step Economy and Function Oriented Synthesis.Tandem Allylboration-Prins Reaction for the Rapid Construction of Substituted Tetrahydropyrans: Application to the Total Synthesis of (-)-Clavosolide A.Enantioselective synthesis of (-)-exiguolide by iterative stereoselective dioxinone-directed Prins cyclizations.A tandem isomerization/prins strategy: iridium(III)/Brønsted acid cooperative catalysisExo-selective reductive macrocyclization of ynals.De novo macrolide-glycolipid macrolactone hybrids: Synthesis, structure and antibiotic activity of carbohydrate-fused macrocycles.Facile access to cis-2,6-disubstituted tetrahydropyrans by palladium-catalyzed decarboxylative allylation: total syntheses of (±)-centrolobine and (+)-decytospolides A and B.Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes.Catalytic intermolecular carbon electrophile induced semipinacol rearrangement.A tandem annulation with a [1,3]-hydride transfer as the key step leading to isochromans.Substitution dependent stereoselective construction of bicyclic lactones and its application to the total synthesis of pyranopyran, tetraketide and polyrhacitide AFabrication of plasmonic Au-Pd alloy nanoparticles for photocatalytic Suzuki-Miyaura reactions under ambient conditions.Stereodivergent Synthesis of Functionalized Tetrahydropyrans Accelerated by Mechanism-Based Allylboration and Bioinspired Oxa-Michael Cyclization.A tandem Prins spirocyclization for the stereoselective synthesis of tetrahydrospiro[chroman-2,4'-pyran] derivatives.Synthesis, structure and reactivity of [15]-macrodilactones.An iodine catalyzed metal free domino process for the stereoselective synthesis of oxygen bridged bicyclic ethers.Total synthesis of (-)-exiguolide via an organosilane-based strategy.Gold-catalyzed 1,2-acyloxy migration/intramolecular [3+2] 1,3-dipolar cycloaddtion cascade reaction: an efficient strategy for syntheses of medium-sized-ring ethers and amines.An Efficient Synthesis of Benzazocines by Gold(I)-Catalyzed Tandem 1,2-Acyloxy Shift/[3+2] Cycloaddition of Terminal 1,9-Enynyl Esters.Synthesis of 3-oxaterpenoids and its application in the total synthesis of (±)-moluccanic acid methyl ester.A natural product inspired tetrahydropyran collection yields mitosis modulators that synergistically target CSE1L and tubulin.Stereoselective Synthesis and Physicochemical Properties of Liquid-Crystal Compounds Possessing atrans-2,5-Disubstituted Tetrahydropyran Ring with Negative Dielectric Anisotropy
P2860
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P2860
Prins-type macrocyclizations as an efficient ring-closing strategy in natural product synthesis.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
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2010年學術文章
@zh-hant
name
Prins-type macrocyclizations a ...... in natural product synthesis.
@en
Prins-type macrocyclizations a ...... in natural product synthesis.
@nl
type
label
Prins-type macrocyclizations a ...... in natural product synthesis.
@en
Prins-type macrocyclizations a ...... in natural product synthesis.
@nl
prefLabel
Prins-type macrocyclizations a ...... in natural product synthesis.
@en
Prins-type macrocyclizations a ...... in natural product synthesis.
@nl
P2860
P356
P1476
Prins-type macrocyclizations a ...... in natural product synthesis.
@en
P2093
Erika A Crane
P2860
P304
P356
10.1002/ANIE.201002809
P407
P577
2010-11-01T00:00:00Z