STILBENE GLYCOSIDES FROM GUIBOURTIA TESSMANNII

DOI: 10.1016/0031-9422(94)00915-G

Source and publish data:

Phytochemistry p. 895 - 898 (1995)

Update date:2022-08-04

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Authors:

Nyemba, A. M.

Mpondo, T. Ngando

Kimbu, S. F.

Connolly, J. D.

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Article abstract of DOI:10.1016/0031-9422(94)00915-G

(E)-3,4'-Dimethoxy-5-rutinosyl stibene, rhaponticin and piceid have been isolated from the stem bark of Guibourtia tessmannii. - Key words: Guibourtia tessmannii; Cesalpiniaceae; stem bark; chemistry; stilbene glycoside.

Full text of DOI:10.1016/0031-9422(94)00915-G

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Article Doi

STILBENE GLYCOSIDES FROM GUIBOURTIA TESSMANNII

DOI: 10.1016/0031-9422(94)00915-G

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0031-9422(94)00915-G

Full text of DOI:10.1016/0031-9422(94)00915-G

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R&D Labs maybe for 106822-44-0

Relevant to this article

Revolutionary phosgene-free synthesis of α-amino acid N-carboxyanhydrides using diphenyl carbonate based on activation of α-amino acids by converting into imidazolium salts

Dehydrative amination of alcohols in water using a water-soluble calix[4]resorcinarene sulfonic acid

Straightforward and regiospecific synthesis of pyrazole-5-carboxylates from unsymmetrical enaminodiketones

OXIDATIVE ADDITION REACTIONS OF CpOS(CO)PMe2Ph)Me (Cp= η⁵ -C5Me5). ISOLATION OF INTERMEDIATES DURING ALKYL-METAL ELECTROPHILIC CLEAVAGE REACTIONS

Article Doi

STILBENE GLYCOSIDES FROM GUIBOURTIA TESSMANNII

DOI: 10.1016/0031-9422(94)00915-G

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0031-9422(94)00915-G

Full text of DOI:10.1016/0031-9422(94)00915-G

Products guided by the article

R&D Labs maybe for 106822-44-0

Relevant to this article

Revolutionary phosgene-free synthesis of α-amino acid N-carboxyanhydrides using diphenyl carbonate based on activation of α-amino acids by converting into imidazolium salts

Dehydrative amination of alcohols in water using a water-soluble calix[4]resorcinarene sulfonic acid

Straightforward and regiospecific synthesis of pyrazole-5-carboxylates from unsymmetrical enaminodiketones

OXIDATIVE ADDITION REACTIONS OF Cp*OS(CO)PMe2Ph)Me (Cp*= η5 -C5Me5). ISOLATION OF INTERMEDIATES DURING ALKYL-METAL ELECTROPHILIC CLEAVAGE REACTIONS

OXIDATIVE ADDITION REACTIONS OF CpOS(CO)PMe2Ph)Me (Cp= η⁵ -C5Me5). ISOLATION OF INTERMEDIATES DURING ALKYL-METAL ELECTROPHILIC CLEAVAGE REACTIONS