The Diene-Transmissive -Cycloaddition Strategy: Stereoselective Synthesis of Advanced Intermediates to Quassinoids

DOI: 10.1021/jo00098a017

Source and publish data:

Journal of Organic Chemistry p. 5596 - 5608 (1994)

Update date:2022-08-04

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Authors:

Spino, Claude

Liu, Gang

Tu, Noah

Girard, Suzanne

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Article abstract of DOI:10.1021/jo00098a017

Complex intermediates to quassinoids, some optically active and containing many functional groups, were synthesized via a diene-transmissive Diels-Alder strategy.The stereochemistry of the key inter- and intramolecular cycloadditions was controlled by ste

Full text of DOI:10.1021/jo00098a017

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Article Doi

The Diene-Transmissive -Cycloaddition Strategy: Stereoselective Synthesis of Advanced Intermediates to Quassinoids

DOI: 10.1021/jo00098a017

Source and publish data:

Authors:

Article abstract of DOI:10.1021/jo00098a017

Full text of DOI:10.1021/jo00098a017

Products guided by the article

R&D Labs maybe for 160084-54-8

Relevant to this article

Differential chemical modification of substrate binding areas in porcine-pancreatic alpha-amylase by three regioisomeric photolabile ligands

Sequential C3 and C5 direct C-H arylation of imidazo[1,2-a]pyrazines with (Hetero)aryl bromides

Diversity-Oriented Approach to Normuscopyridine and Its Analogues through Ring-Closing Metathesis

An efficient synthesis of pyrido[2,3-d][6,5-d]dipyrimidine and 5,5′-arylmethylenebis(2,6-diaminopyrimidinone) derivatives under microwave irradiation

Facile preparation of dehydrodigallic acid and its derivative for the synthesis of ellagitannins

Experimental and theoretical studies of (FTIR, FT-NMR, UV-Visible, X-ray and DFT) 2-(4-Allyl-5-pyridin-4-yl-4H-[1,2,4]triazol-3-ylsulfanyl)-1-(3-methyl- 3-phenyl-cyclobutyl)-ethanone