Pheromone synthesis, CXLVII. – Synthesis of (1R,3S,6R,9S,10S)-9,10-Epoxytetrahydroedulan, the Main Component of the Hairpencil Secretion of Male Danaid ButterflyEuploea klugii-Reference-Cited by-同舟云学术

Pheromone synthesis, CXLVII. – Synthesis of (1R,3S,6R,9S,10S)-9,10-Epoxytetrahydroedulan, the Main Component of the Hairpencil Secretion of Male Danaid ButterflyEuploea klugii

Published:1993-01-21 Issue:1 Volume:1993 Page:83-90
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Mori Kenji,Aki Shinji,Kido Masaru

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Reference16 articles.

1. Part CXLVI: , Biosci. Biotech. Biochem., in press.

2. [2a] , , , , Liebigs Ann. Chem. 1989, 1195–1201.

3. [2b] – A comparison of our spectra with the originals provided by Prof. Francke revealed a misprint in ref.[2a]: the 13C-NMR spectrum of 14 shows a signal at δ = 34.74 and not at δ = 35.33.

4. [2c] – A comparison of our spectra with the originals provided by Prof. Francke revealed a misprint in ref.[2a]: the 13C-NMR spectrum of 1 shows a signal at δ = 73.47 and not at δ = 70.25.

5. Terpenoids from bark beetles, solitary bees and danaine butterflies

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