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2006 | 4 | 3 | 375-402
Tytuł artykułu

Heteroareno-annelated estranes by triene cyclization

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
17-Thienyl-and 17-benzo[b]thienyl-3-hydroxyestra-1,3,5(10),16-tetraenes were synthesized by either sequential or one-pot Suzuki cross-coupling and Wittig olefination reactions. At 160 °C, heteroaryl substituted steroids were observed to undergo thermal intramolecular cyclization to produce E-ring heteroareno-annelated estranes.
Słowa kluczowe
Wydawca

Czasopismo
Rocznik
Tom
4
Numer
3
Strony
375-402
Opis fizyczny
Daty
wydano
2006-09-01
online
2006-09-01
Twórcy
  • Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, Kasuga-shi, 816-8580, Japan
  • Institute of Materials Chemistry and Engineering, Kyushu University, Kasuga-shi, 816-8580, Japan
  • Institute of Materials Chemistry and Engineering, Kyushu University, Kasuga-shi, 816-8580, Japan
  • Institute of Materials Chemistry and Engineering, Kyushu University, Kasuga-shi, 816-8580, Japan, thies@cm.kyushu-u.ac.jp
Bibliografia
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  • [26] M. Watanabe, G.R. Morais, S. Mataka, K. Ideta and T. Thiemann: “Two Variations of Solvent-Reduced Wittig Olefination Reactions - Comparison of Solventless Wittig Reactions to Wittig Reactions under Ultrasonication with Minimal Work-up”, Z. f. Naturforschg., Vol. 60B, (2005), p. 909.
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Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_s11532-006-0016-2
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