Absolute configurations of all four stereoisomers of cryptocaryalactone and deacetyl cryptocaryalactone-Reference-Cited by-同舟云学术

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Absolute configurations of all four stereoisomers of cryptocaryalactone and deacetyl cryptocaryalactone

Published:1998-11 Issue:6 Volume:49 Page:1683-1687
ISSN:0031-9422
Container-title:Phytochemistry
language:en
Short-container-title:Phytochemistry

Author:

Drewes Siegfried E,Horn Marion M,Ramesar Niyum S,Ferreira Daneel,Nel Reinier J.J,Hutchings Anne

Publisher

Elsevier BV

Subject

Horticulture,Plant Science,Molecular Biology,General Medicine,Biochemistry

Reference8 articles.

1. (−)-Cryptocaryalactone and (−)-deacetylcryptocaryalactone-germination inhibitors from Cryptocarya moschata seeds

2. Meyer, H. H., Liebigs Annalen der Chemie, 1984, 977

3. Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters

4. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

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1. First diastereoselective total synthesis of bicyclic styryl lactone: (1R,5R,7R)-7-((E)-styryl)-2,6-dioxabicyclo[3.3.1]nonan-3-one;Results in Chemistry;2023-01

2. α-Pyrones with glucose uptake-stimulatory activity from the twigs of Cryptocarya wrayi;Fitoterapia;2022-04

3. 5,6-Dihydro-α-pyrones from the leaves of Cryptocarya pulchinervia (Lauraceae);Journal of Natural Medicines;2020-03-23

4. Recent advances in the applications of Wittig reaction in the total synthesis of natural products containing lactone, pyrone, and lactam as a scaffold;Monatshefte für Chemie - Chemical Monthly;2019-07-19

5. Chemoenzymatic total synthesis of cryptocaryalactone natural products;Tetrahedron Letters;2018-01

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