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F. Löwe Teichmann Prausnitz R. E. Liesegang Hans Pfeiffer 《Colloid and polymer science》1935,71(3):354-356
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M. N. Bazhin 《Theoretical and Experimental Chemistry》1981,16(5):498-501
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E. Geissler 《Analytical and bioanalytical chemistry》1903,42(6-7):463-463
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《Journal of Analytical Chemistry》2010,65(9):983-984
Chronicle
Birthday of academician B. F. Myasoedov 相似文献16.
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[Chemical reaction: See text] The synthesis of stevastelin B3 (2) and B (5) are described. In a first approach, epoxy cyclodepsipeptide 8 was considered as a promising candidate for the synthesis of the [15]-membered ring members of the stevastelins; however, the oxirane ring opening, required for the completion of the natural stevastelin synthesis, failed. Thus, we synthesized stevastelin B (5), carrying out the oxirane ring opening earlier in the synthesis and following a synthetic scheme capable of delivering analogues. On the other hand, a translactonization reaction of the [15]-membered ring derivative 59 led to the total synthesis of the natural [13]-membered ring component of the stevastelins family, stevastelin B3 (2). 相似文献
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《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2015,127(10):2924-2924