New Synthesis of Penta-N,O-acetyl-DL-validamine and Pseudo-2-amino-2-deoxy-α-DL-mannopyranose, and Their Uronate Analogs

DOI: 10.1246/bcsj.61.1824

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1824 - 1826 (1988)

Update date:2022-07-29

Topics:

Authors:

Ogawa, Seiichiro

Suzuki, Motohiro

Tonegawa, Takeshi

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Article abstract of DOI:10.1246/bcsj.61.1824

Treatment of the hydroxy lactone derived from (+/-)-endo-7-oxabicyclo<2.2.1>hept-5-ene-2-carboxylic acid with hydrogen bromide-acetic acid, followed by esterification, gave 48 percent of ethyl DL-(1,3,5/2,4)-5-bromo-2,3,4-trihydroxy-1-cyclohexanecarboxyla

Full text of DOI:10.1246/bcsj.61.1824

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Article Doi

New Synthesis of Penta-N,O-acetyl-DL-validamine and Pseudo-2-amino-2-deoxy-α-DL-mannopyranose, and Their Uronate Analogs

DOI: 10.1246/bcsj.61.1824

Source and publish data:

Authors:

Article abstract of DOI:10.1246/bcsj.61.1824

Full text of DOI:10.1246/bcsj.61.1824

Products guided by the article

R&D Labs maybe for 117683-13-3

Relevant to this article

Intramolecular chirality transfer in irans-5,6-Diaryl-5,6-dihydro-l,10- phenanthroline-5,6-diols: Solvato- And halochromic responses by circular dichroism

Chiral bioinspired non-heme iron complexes for enantioselective epoxidation of α,β-unsaturated ketones

The preparation and X-ray crystal structure of (SC6F5)2-2)>2>

Sterically oriented synthesis and structure of new perphosphorylated resorcinarenes

EPR spectroscopic investigation of radical-induced degradation of partially fluorinated aromatic model compounds for fuel cell membranes

FURANNULATION via RADICAL CYCLISATION