Synthesis of Strychnos Alkaloids PDF Download
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Author: Christopher Scott Brook
Publisher:
ISBN:
Category : Alkaloids
Languages : en
Pages : 734
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Book Description
Author: Christopher Scott Brook
Publisher:
ISBN:
Category : Alkaloids
Languages : en
Pages : 734
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Book Description
Author: Gopal Sirasani
Publisher: Elsevier Inc. Chapters
ISBN: 0128056045
Category : Science
Languages : en
Pages : 39
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Book Description
Described herein is an account of my laboratory’s entry into the magnificent field of complex alkaloid total synthesis, spanning the development of novel methods for quickly assembling polycyclic frameworks through the total synthesis of various members of the Strychnos alkaloids. A discussion of the prior art related to our approach to these alkaloids in addition to strategic decisions and reasoning made en route to targets akuammicine ( 1 ), strychnine ( 2 ), and leuconicines A ( 3 ) and B ( 4 ) is carefully detailed. Finally, we present the retrosynthetic analyses of the aforementioned targets and respective total syntheses thereof (including asymmetric variants).
Author: Steven Roger Angle
Publisher:
ISBN:
Category :
Languages : en
Pages : 428
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Book Description
Author: Albert Peter Paul
Publisher:
ISBN:
Category : Alkaloids
Languages : en
Pages : 236
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Author: Johannes Nicolaas Zonjee
Publisher:
ISBN:
Category :
Languages : en
Pages : 136
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Book Description
Author: Robert Wells Marquis
Publisher:
ISBN:
Category :
Languages : en
Pages : 260
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Author: Christophe Michoud
Publisher:
ISBN:
Category :
Languages : en
Pages : 414
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Author: David Bruce Coakwell Martin
Publisher:
ISBN: 9781267029607
Category :
Languages : en
Pages : 471
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Book Description
In the first part of this dissertation, our studies toward the Strychnos alkaloids are detailed. Previous work in this area is summarized in Chapter 1, including a short description of the biosynthetic pathway, a discussion of the structural challenges of the Strychnos alkaloids, and unique strategies that have been developed to overcome these challenges. An introduction to the use of Zincke aldehydes in natural product synthesis is presented in Chapter 2, including important historical examples and the work developed in the Vanderwal group. In Chapter 3, the development of the anionic bicyclization of tryptamine-derived Zincke aldehydes is outlined, along with substrate scope and preliminary mechanistic discussions. The bicyclization reaction provides tetracyclic products in moderate to high yields and as single diastereomers, matching the ABCE ring system of most indole monoterpene alkaloids. The application of this reaction to the synthesis of norfluorocurarine is discussed. In Chapter 4, a second-generation strategy for gaining general access to more complex tetracyclic compounds is outlined. The allyl group was identified as an easily removed protecting group, allowing the subsequent incorporation of more complex side-chains. A number of strategies for Strychnos D-ring closure were explored, including a propargylsilane cyclization, Heck reaction and Cu-mediated conjugate addition. Concise syntheses of norfluorocurarine (five steps), dehydrodesacetylretuline (six steps), valparicine (seven steps), the Wieland-Gumlich aldehyde (five steps) and strychnine (six steps) are disclosed. Unexpected reactions discovered during our studies include a surprisingly facile dimerization of the products, and an unexpected cycloreversion to regenerate Zincke aldehydes under specific conditions. In the second part of this dissertation, our progress toward the synthesis of platencin, a novel antibiotic, is described. The proposed synthesis incorporates a bicyclization strategy that was explored using a radical cascade reaction, a Heck reaction, and related stepwise approaches. While attempting to photoinitiate an atom-tranfer radical cyclization, a [2+2] adduct was isolated and characterized by X-ray diffraction. A variety of thermally initiated reactions are also described, giving different products, including small quantities of a tricyclic product that closely resembles the desired product, but could not be unambiguously characterized. Using a Heck reaction, cyclization could not complete with ß-hydride elimination. A two-step cyclization sequence was also attempted, without success.
Author: William Banks Hinshaw
Publisher:
ISBN:
Category : Alkaloids
Languages : en
Pages : 308
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Book Description
Author: Praveen Kokkonda
Publisher:
ISBN:
Category :
Languages : en
Pages : 232
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Book Description
The Strychnos class of indole alkaloids contain a pyrrolo[2,3-d]carbazole ABCE tetracyclic framework. The second-generation ABCE tetracycle approach was employed in the total synthesis of (±)-20-epi-lochneridine and progress toward total synthesis of (±)-alstolucine B. The second-generation approach featured Mitsunobu activation of the hydroxyethyl group in a gramine intermediate followed by intramolecular aza-Baylis-Hillman reaction. The substrate for hydroboration was redesigned to (±)-18-desmethyl akuammicine (1,1-disubstituted double bond), since the hydroboration of trisubstituted alkenes afforded tertiary alcohol via Markovnikov addition. The key steps were n-Bu3SnH mediated cyclization reaction to accomplish D-ring, tert-butyl hypochlorite indoline oxidation, and anti-Markovnikov hydroboration to introduce a primary alcohol. The total syntheses of Strychnos-Strychnos type bis-indole alkaloids (−)-leucoridine A and C were accomplished from the biomimetic dimerization of (−)-dihydrovalparicine. En route to (−)-dihydrovialparicine, known alkaloids (+)-geissoschizoline and (−)-dehydrogeissoschizoline were also prepared from commercially available N-tosyl indole 3-carboxaldehyde. Key steps consisted of an in situ dimerization of (−)-dihydrovalparicine from (−)-1, 2-dehydrogeissoschizoline with trifluoroacetic acid in the presence of 4 Å molecular sieves. Acid mediated ring-opening of the indolenine in (−)-leucoridine A to afford (−)-leucoridine C. DFT calculations were employed to elucidate the mechanism of dimerization, which suggested that a stepwise aza-Michael/spirocyclization sequence was preferred over the alternate hetero Diels-Alder cycloaddition reaction. A novel domino Michael/Mannich [4+2] annulation method was applied for concise total synthesis of Aspidospermatan alkaloids (+)-20-epi-condyfoline and progress toward the total synthesis of (+)-condyfoline. The additional key steps consisted of a LiHMDS mediated cyclization to form D-ring, dimethyl(methylthio)sulfonium tetrafluoroborate (DMTSF) mediated spirocyclization to form pentacyclic thioether and indoline oxidation with MnO2.
