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Total synthesis of oasomycin A.
~
Harvard University.
Total synthesis of oasomycin A.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Total synthesis of oasomycin A.
作者:
Nagorny, Pavel.
面頁冊數:
262 p.
附註:
Source: Dissertation Abstracts International, Volume: 68-02, Section: B, page: 0981.
Contained By:
Dissertation Abstracts International68-02B.
標題:
Chemistry, Organic.
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3251301
Total synthesis of oasomycin A.
Nagorny, Pavel.
Total synthesis of oasomycin A.
- 262 p.
Source: Dissertation Abstracts International, Volume: 68-02, Section: B, page: 0981.
Thesis (Ph.D.)--Harvard University, 2007.
*Please refer to dissertation for diagram.Subjects--Topical Terms:
193634
Chemistry, Organic.
Total synthesis of oasomycin A.
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Total synthesis of oasomycin A.
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Source: Dissertation Abstracts International, Volume: 68-02, Section: B, page: 0981.
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Thesis (Ph.D.)--Harvard University, 2007.
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*Please refer to dissertation for diagram.
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The NMR-based structural assignment of the absolute and relative stereochemistry was confirmed by comparison of natural oasomycin A to the sample obtained by synthesis described herein.*
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The total synthesis of the macrolide oasomycin A is described. The convergent synthesis strategy divided this macrolide into five main fragments. These fragments were synthesized via aldol-based methodology and coupled. Key fragment couplings included an anti-Felkin selective aldol addition to construct the C28--C29 bond, Kociensky-Julia olefinations to construct the Delta12 and Delta38 olefins, and a competitive Weinreb amide acylation reaction to fashion the C21 --C22 bond. The utility of 4,5-diphenyloxazole as a carboxy surrogate has been demonstrated throughout the synthesis. The results of a systematic investigation of the late-stage macrolactonization that generated the 42-membered macrocycle of oasomycin A are also presented.
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