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The Total Synthesis of the Proposed Structure of Mycosporulone and the Enantiospecific Formal Total Synthesis of (+)-FawcettimineThe Total Synthesis of the Proposed Structure of Mycosporulone and the Enantiospecific Formal Total Synthesis of (+)-Fawcettimine pdf free

The Total Synthesis of the Proposed Structure of Mycosporulone and the Enantiospecific Formal Total Synthesis of (+)-Fawcettimine


Author: Heather R Harding
Published Date: 08 Sep 2011
Publisher: Proquest, Umi Dissertation Publishing
Original Languages: English
Book Format: Paperback::206 pages
ISBN10: 1243732105
ISBN13: 9781243732101
File size: 44 Mb
Dimension: 189x 246x 11mm::376g
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Enantiospecific Total Synthesis of ( )-Bakkenolide III and Formal Total which also constitutes the formal total synthesis of ( )-bakkenolides, B, C, H, L, V, and X. Synthesis of the Core Structure of Daphnimacropodines. Organic and a synthetic study of the formal synthesis of enantiopure fawcettimine. Total synthesis of the proposed structure of mycosporulone: structural revision and an unexpected Enantiospecific formal total synthesis of (+)-fawcettimine. Abstract A formal total synthesis of the marine macrolide iriomoteolide 3a is described. Salient features of the synthesis include the elaboration Enantiospecific Formal Total Synthesis of (+)-Fawcettimine intermediate in Heathcock's synthesis, there completing a formal total synthesis





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