Phosphoric acid catalyzed desymmetrization of bicyclic bislactones bearing an all-carbon stereogenic center: total syntheses of (-)-rhazinilam and (-)-leucomidine B.

Phosphoric acid catalyzed desymmetrization of bicyclic bislactones bearing an all-carbon stereogenic center: total syntheses of (-)-rhazinilam and (-)-leucomidine B.

Item
http://www.wikidata.org/entity/Q53495374
Selective syntheses of leuconolam, leuconoxine, and mersicarpine alkaloids from a common intermediate through regiocontrolled cyclizations by Staudinger reactions†Electronic supplementary information (ESI) available: Experimental details and proceduA Functional Group Approach for Prediction of APPI Response of Organic Synthetic Targets.Discovery and enantiocontrol of axially chiral urazoles via organocatalytic tyrosine click reaction.The Diaza[5.5.6.6]fenestrane Skeleton-Synthesis of Leuconoxine Alkaloids.Biosynthetically inspired divergent approach to monoterpene indole alkaloids: total synthesis of mersicarpine, leuconodines B and D, leuconoxine, melodinine E, leuconolam, and rhazinilam.Palladium-Catalyzed Enantioselective Desymmetrizing Aza-Wacker Reaction: Development and Application to the Total Synthesis of (-)-Mesembrane and (+)-Crinane.Enantioselective Brønsted Acid Catalysis as a Tool for the Synthesis of Natural Products and Pharmaceuticals.Organocatalytic Enantioselective Acyloin Rearrangement of α-Hydroxy Acetals to α-Alkoxy Ketones.Organocatalytic Nucleophilic Addition of Hydrazones to Imines: Synthesis of Enantioenriched Vicinal Diamines.Free-Radical Carbocyanation of Olefins.Organocatalytic Enantioselective Vinylogous Pinacol Rearrangement Enabled by Chiral Ion Pairing.Chiral Phosphoric Acid-Catalyzed Enantioselective Formal [3+2] Cycloaddition of Azomethine Imines with Enecarbamates.Enantioselective Total Syntheses of (-)-Rhazinilam, (-)-Leucomidine B, and (+)-Leuconodine F.Catalytic Silylations of Alcohols: Turning Simple Protecting-Group Strategies into Powerful Enantioselective Synthetic Methods.Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations.
P2860

Phosphoric acid catalyzed desymmetrization of bicyclic bislactones bearing an all-carbon stereogenic center: total syntheses of (-)-rhazinilam and (-)-leucomidine B.

Item
http://www.wikidata.org/entity/Q53495374
description
2014 nî lūn-bûn
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name
Phosphoric acid catalyzed desy ...... zinilam and (-)-leucomidine B.
@en
Phosphoric acid catalyzed desy ...... nic center: total syntheses of
@nl
type
label
Phosphoric acid catalyzed desy ...... zinilam and (-)-leucomidine B.
@en
Phosphoric acid catalyzed desy ...... nic center: total syntheses of
@nl
prefLabel
Phosphoric acid catalyzed desy ...... zinilam and (-)-leucomidine B.
@en
Phosphoric acid catalyzed desy ...... nic center: total syntheses of
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P356
P1433
P1476
Phosphoric acid catalyzed desy ...... zinilam and (-)-leucomidine B.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698