Ostopanic acid and ethyl 6-oxodocosa-2,4-dienoate were synthesized by a short route based on the palladium catalyzed isomerization of ynone and ynoic ester, respectively, using pent-4-ynal as a starting material. There $re variouf classes 04f natural products such as alcohols, 1 aldehydes, ketones,
โฆ LIBER โฆ
A facile and efficient stereoselective synthesis of 6-hydroxy-trans-4a-phenyldecahydroisoquinoline
โ Scribed by Shinzo Kano; Tsutomu Yokomatsu; Yoko Yuasa; Shiroshi Shibuya
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 144 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
A stereoselective synthesis of 6-oxygenated trans-4a-phenyldecahydroisoquinoline was achieved by treatment of l-ethoxycarbamoyl-l-phenyl-l,S-hexadiene with paraformaldehyde in formic acid.
We investigated a stereoselective synthesis of 6-oxygenated trans-4a-phenyldecahydroisoquinoline system, a key structural variant of morphine moleculel.
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## Abstract For Abstract see ChemInform Abstract in Full Text.
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