Author: Barry George Shearer
Publisher:
ISBN:
Category : Ring formation (Chemistry)
Languages : en
Pages : 426
Book Description
Studies Toward the Total Synthesis of Kijanolide
Author: Barry George Shearer
Publisher:
ISBN:
Category : Ring formation (Chemistry)
Languages : en
Pages : 426
Book Description
Publisher:
ISBN:
Category : Ring formation (Chemistry)
Languages : en
Pages : 426
Book Description
A Formal Synthesis of Tetronolide Studies Toward the Total Synthesis of Kijanolide
Author: Melissa Lynn Reilly
Publisher:
ISBN:
Category :
Languages : en
Pages : 364
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 364
Book Description
Studies Toward the Synthesis of Kijanolide
Author: Bradley B. Brown
Publisher:
ISBN:
Category :
Languages : en
Pages : 606
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 606
Book Description
Studies Toward the Total Synthesis of the Tedanolides
Author: Lisa Deanna Julian
Publisher:
ISBN:
Category :
Languages : en
Pages : 416
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 416
Book Description
Part I. Total Synthesis of (-)-ratjadone Part II. Studies Toward the Total Synthesis of Zoanthenol
Author: David C. Ihle
Publisher:
ISBN:
Category :
Languages : en
Pages : 532
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 532
Book Description
Studies Toward the Total Synthesis of Quartromicin D3
Author: Roxanne Kay Kunz
Publisher:
ISBN:
Category :
Languages : en
Pages : 272
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 272
Book Description
Studies Toward the Total Synthesis of Glycinoeclepin A
Author: Charnsak Thongsornkleeb
Publisher:
ISBN:
Category :
Languages : en
Pages : 188
Book Description
Studies directed toward the synthesis of the A-ring portion of glycinoeclepin A are described. The enantioselective synthesis of key diketone intermediate 128 in four steps from 2,2-dimethyl-1,3-cyclohexanedione (5) has been accomplished via the acid-catalyzed intramolecular Michael cyclization of an enone generated in situ from 132. In the course of these studies, a new method for the preparation of the highly reactive a-alkynyl acroleins was developed. Several methods for the further elaborations of diketone 128 to the key enyne intermediate 95 were investigated and the best route developed to date involves the conversion of the methyl ketone to a vinyl triflate (177) followed by Sonogashira coupling. In addition, the conversion of diketone 128 to the vinyl halide 258 via a Shapiro strategy was achieved and model studies were carried out on the synthesis of vinylallene by coupling cuprate derivatives of this intermediate with propargyl alcohol derivatives.
Publisher:
ISBN:
Category :
Languages : en
Pages : 188
Book Description
Studies directed toward the synthesis of the A-ring portion of glycinoeclepin A are described. The enantioselective synthesis of key diketone intermediate 128 in four steps from 2,2-dimethyl-1,3-cyclohexanedione (5) has been accomplished via the acid-catalyzed intramolecular Michael cyclization of an enone generated in situ from 132. In the course of these studies, a new method for the preparation of the highly reactive a-alkynyl acroleins was developed. Several methods for the further elaborations of diketone 128 to the key enyne intermediate 95 were investigated and the best route developed to date involves the conversion of the methyl ketone to a vinyl triflate (177) followed by Sonogashira coupling. In addition, the conversion of diketone 128 to the vinyl halide 258 via a Shapiro strategy was achieved and model studies were carried out on the synthesis of vinylallene by coupling cuprate derivatives of this intermediate with propargyl alcohol derivatives.
Studies Toward the Total Synthesis of Aplysistatin and the Total Synthesis of Ancistrofuran
Author: Andrew James Caruso
Publisher:
ISBN:
Category :
Languages : en
Pages : 438
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 438
Book Description
Total Synthesis of Cylindricines A and B
Author: Julie Elizabeth Fields
Publisher:
ISBN:
Category :
Languages : en
Pages : 362
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 362
Book Description
Studies Toward the Total Synthesis of ( )-Cortistatin J Via an Intramolecular (4 3) Cycloaddition
Author: Lok-Lok Liu
Publisher:
ISBN: 9781361255162
Category :
Languages : en
Pages :
Book Description
This dissertation, "Studies Toward the Total Synthesis of ( )-cortistatin J via an Intramolecular (4 3) Cycloaddition" by Lok-lok, Liu, 廖樂樂, was obtained from The University of Hong Kong (Pokfulam, Hong Kong) and is being sold pursuant to Creative Commons: Attribution 3.0 Hong Kong License. The content of this dissertation has not been altered in any way. We have altered the formatting in order to facilitate the ease of printing and reading of the dissertation. All rights not granted by the above license are retained by the author. DOI: 10.5353/th_b4659162 Subjects: Ring formation (Chemistry) Organic compounds - Synthesis
Publisher:
ISBN: 9781361255162
Category :
Languages : en
Pages :
Book Description
This dissertation, "Studies Toward the Total Synthesis of ( )-cortistatin J via an Intramolecular (4 3) Cycloaddition" by Lok-lok, Liu, 廖樂樂, was obtained from The University of Hong Kong (Pokfulam, Hong Kong) and is being sold pursuant to Creative Commons: Attribution 3.0 Hong Kong License. The content of this dissertation has not been altered in any way. We have altered the formatting in order to facilitate the ease of printing and reading of the dissertation. All rights not granted by the above license are retained by the author. DOI: 10.5353/th_b4659162 Subjects: Ring formation (Chemistry) Organic compounds - Synthesis