## Abstract Calixarene analogs containing a thiophene unit in the macrocyclic ring were prepared by a stepwise method. The macrocycles adopt a coneβlike form as the preferred conformation in solution. The induced chemical shift change, nOe experiment, and ^1^H relaxation time (__T__~1~) measurement
Toward the synthesis of taxol and its analogs: Incorporation of non-aromatic C-rings in the pinene pathway
β Scribed by Paul A. Wender; Paul E. Floreancig; Timothy E. Glass; Michael G. Natchus; Anthony J. Shuker; James C. Sutton
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 229 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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The paper reports the synthesis of some ethereal insect juvenile hormone analogs with a pinene or cyclohexene ring in the terminal position. ## Synthese von Juvenilhormon-Analogen von Insekten, IV I). -Synthese von Ether-Analogen mit einem Pinen-und Cyclohexenring in der terminalen Stellung Es wi
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