Concise Total Synthesis of Enigmazole A & Studies Towards the Total Synthesis of Rhizoxin D

Concise Total Synthesis of Enigmazole A & Studies Towards the Total Synthesis of Rhizoxin D PDF Author: Andreas Ahlers
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Languages : en
Pages :

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Concise Total Synthesis of Enigmazole A & Studies Towards the Total Synthesis of Rhizoxin D

Concise Total Synthesis of Enigmazole A & Studies Towards the Total Synthesis of Rhizoxin D PDF Author: Andreas Ahlers
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Category :
Languages : en
Pages :

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The Total Synthesis of Rhizoxin D

The Total Synthesis of Rhizoxin D PDF Author: Kim Werner
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ISBN:
Category :
Languages : en
Pages : 312

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Total Synthesis of (+)-rhizoxin D.

Total Synthesis of (+)-rhizoxin D. PDF Author: Jeffrey Paul Stonehouse
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Category :
Languages : en
Pages :

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Studies Directed Toward the Total Synthesis of (-)-enigmazole B

Studies Directed Toward the Total Synthesis of (-)-enigmazole B PDF Author: Alia M. Orbin
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Category :
Languages : en
Pages : 247

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Total Synthesis of (-)-enigmazole A

Total Synthesis of (-)-enigmazole A PDF Author: Yanran Ai
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Category :
Languages : en
Pages : 530

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The dissertation contained herein presents a total synthesis of (-)-enigmazole A utilizing a late-stage large-fragment Petasis-Ferrier union/rearrangement protocol. Chapter One details the isolation, structural elucidation and subsequent biological studies of (-)-enigmazole A. The previous synthetic studies of (-)-enigmazole A are also introduced. The chapter then outlines the Smith three-step Petasis-Ferrier union/rearrangement protocol, as well as a number of the successfultotal syntheses achieved over the years by the Smith group utilizing this protocol. Herein, a late-stage large-fragment Petasis-Ferrier union/rearrangement will be utilized as the synthetic cornerstone for the Smith total synthesis of (-)-enigmazole A. Chapter Two describes the retrosynthetic strategy toward (-)-enigmazole A and subsequent total synthesis. The late-stage large-fragment Petasis-Ferrier union/rearrangement, which generates the entire carbon skeletonof (-)-enigmazole A, is described after the construction of the requisite eastern and western hemispheres. The chapter then describes the subsequent macrolactonization studies and the end game of the total synthesis. In addition to the Smith three-step Petasis-Ferrier union/rearrangement protocol, highlights of the total synthesis includes a Negishi cross-coupling, a dithiane-epoxide union, a Type I ARC multicomponent coupling, a Yamaguchi macrolactonization and chemoselective oxidation/reduction strategies the details of which are also described in Chapter Two.

Studies Directed Towards the Total Synthesis of Rhizoxin

Studies Directed Towards the Total Synthesis of Rhizoxin PDF Author: Benjamin Eric Blass
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ISBN:
Category :
Languages : en
Pages : 490

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Total Synthesis of (−)‐Enigmazole A.

Total Synthesis of (−)‐Enigmazole A. PDF Author:
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Languages : en
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Studies Directed Toward the Total Synthesis of Rhizoxins

Studies Directed Toward the Total Synthesis of Rhizoxins PDF Author: Jian Hong
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Category :
Languages : en
Pages : 558

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Part A. Studies Directed Towards the Total Synthesis of (±) A-23187 ; Part B. Formal Total Synthesis of (±) A-23187

Part A. Studies Directed Towards the Total Synthesis of (±) A-23187 ; Part B. Formal Total Synthesis of (±) A-23187 PDF Author: Eric L. Williams
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Category : Organic compounds
Languages : en
Pages : 164

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Studies Towards the Total Synthesis of the Biologically Active Natural Product Aigialomycin D and Development of Two Novel Methodologies

Studies Towards the Total Synthesis of the Biologically Active Natural Product Aigialomycin D and Development of Two Novel Methodologies PDF Author: Naval Bajwa
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Category :
Languages : en
Pages : 674

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