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Asymmetric synthesis of naturally occurring spiroketals.

Asymmetric synthesis of naturally occurring spiroketals.

http://www.wikidata.org/entity/Q37270393

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Polyketide assembly by alkene-alkyne reductive cross-coupling: spiroketals through the union of homoallylic alcohols Spiroacetal formation through telescoped cycloaddition and carbon-hydrogen bond functionalization: total synthesis of bistramide A.A gold-catalyzed alkyne-diol cycloisomerization for the synthesis of oxygenated 5,5-spiroketals.Olefin metathesis-iodoetherification-dehydroiodination strategy for spiroketal subunits of polyether antibiotics Construction of spirolactones with concomitant formation of the fused quaternary centre--application to the synthesis of natural products.Asymmetric synthesis of highly functionalized tetrahydropyrans via a one-pot organocatalytic Michael/Henry/ketalization sequence.On the proposed structures and stereocontrolled synthesis of the cephalosporolides.Synthesis of natural products containing spiroketals via intramolecular hydrogen abstraction.A catalytic multicomponent coupling reaction for the enantioselective synthesis of spiroacetals.Synthesis of spiroketals under neutral conditions via a type III ring-rearrangement metathesis strategy

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Asymmetric synthesis of naturally occurring spiroketals.

http://www.wikidata.org/entity/Q37270393

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 28 August 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Asymmetric synthesis of naturally occurring spiroketals.

@en

Asymmetric synthesis of naturally occurring spiroketals.

@nl

type

label

Asymmetric synthesis of naturally occurring spiroketals.

@en

Asymmetric synthesis of naturally occurring spiroketals.

@nl

prefLabel

Asymmetric synthesis of naturally occurring spiroketals.

@en

Asymmetric synthesis of naturally occurring spiroketals.

@nl

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Asymmetric synthesis of naturally occurring spiroketals.

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Anil K Saikia

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B Rama Raju

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Creative Commons Attribution

P2860

Enantioselective total synthesis of bistramide A

1,n-Dicarbanionic Titanium Intermediates from Monocarbanionic Organometallics and Their Application in Organic Synthesis

Stimulation of protein kinase C-dependent and -independent signaling pathways by bistratene A in intestinal epithelial cells

Efficacious modification of the mitsunobu reaction for inversions of sterically hindered secondary alcohols

A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)

Chemistry of spiroketals

Synthesis and activity of a new generation of ruthenium-based olefin metathesis catalysts coordinated with 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ligands.

Total synthesis of bistramide A.

Total synthesis of a stereoisomer of bistramide C and assignment of configuration of the natural product.

The development of L2X2Ru=CHR olefin metathesis catalysts: an organometallic success story.

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1942-2038

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scholarly article

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10.3390/MOLECULES13081942

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18794795

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polycyclic compound

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