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Polyquinane Chemistry - Annette M. Doherty
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Annette M. Doherty:

Polyquinane Chemistry - Livro de bolso

2012, ISBN: 3642726003

[EAN: 9783642726002], Neubuch, [PU: Springer Berlin Heidelberg Mrz 2012], SYNTHESIS; CONGENER; CYCLOADDITION; TERPENE; BIOSYNTHESIS; CRYSTAL; CRYSTALSTRUCTURE; DEVELOPMENT; INSECTICIDE; I… mais…

NEW BOOK. Custos de envio:Versandkostenfrei. (EUR 0.00) BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germany [57449362] [Rating: 4 (von 5)]
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Annette M. Doherty:

Polyquinane Chemistry - Livro de bolso

2006, ISBN: 9783642726002

[ED: Taschenbuch], [PU: Springer Berlin Heidelberg], Neuware - New methods for the construction of condensed five-membered ring systems continue to be developed at an accelerated pace. Th… mais…

Custos de envio:Versandkostenfrei, Versand nach Deutschland. (EUR 0.00) BuchWeltWeit Inh. Ludwig Meier e.K.
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Polyquinane Chemistry
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Polyquinane Chemistry - novo libro

ISBN: 9783642726002

New methods for the construction of condensed five-membered ring systems continue to be developed at an accelerated pace. The challenges underlying this tremendous current upsurge of inte… mais…

Nr. 978-3-642-72600-2. Custos de envio:Worldwide free shipping, , DE. (EUR 0.00)
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Paquette, Leo A.:
Polyquinane Chemistry: Syntheses and Reactions (Reactivity and Structure: Concepts in Organic Chemistry, 26) - Livro de bolso

ISBN: 9783642726002

paperback. Good. Access codes and supplements are not guaranteed with used items. May be an ex-library book., 2.5

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Leo A. Paquette:
Polyquinane Chemistry: Syntheses and Reactions (Reactivity and Structure: Concepts in Organic Chemistry) - Livro de bolso

2012, ISBN: 9783642726002

Springer, 2012. Paperback. New. 244 pages. 9.61x6.69x0.55 inches., Springer, 2012, 6

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Polyquinane Chemistry: Syntheses and Reactions: 26 (Reactivity and Structure: Concepts in Organic Chemistry, 26)

New methods for the construction of condensed five-membered ring systems continue to be developed at an accelerated pace. The challenges underlying this tremendous current upsurge of interest arise from several directions. One stems from the desire to elucidate and resolve those special problems associated with the incorporation of added strain not present when six-membered rings are mutually fused. The many structurally interesting polyquinane natural products isolated and characterized in recent years have provided a particularly delightful forum for application of various new synthetic protocols, many of which must equally well accommodate the particular stereochemical demands of each indi­ vidual target. Synthetic elaboration of a marvellous array of new unnatural molecules also holds continued fascination. In the past, we have attempted to keep others abreast of developments in this rapidly burgeoning area by authoring a pair of comprehensive reviews in Topics in Current Chemistry that appeared in 1979 [1] and 1984 [2]. During this period, others have also surveyed the developments in cyclopentannulation [3] and the cyclopentanoid field in general [4]. In the last couple of years, the pace at which new synthetic facets have been reported has become more frenetic than ever before. Accordingly, a suitable updating of the exciting newer findings was deemed appropriate and the present overview, which extends approximately to mid - 1986, was written. Once again, our hope is that compilations of this type will serve to stimulate imaginative new scientific ventures that will propel the field forward to still greater maturity.

Dados detalhados do livro - Polyquinane Chemistry: Syntheses and Reactions: 26 (Reactivity and Structure: Concepts in Organic Chemistry, 26)


EAN (ISBN-13): 9783642726002
ISBN (ISBN-10): 3642726003
Livro de bolso
Ano de publicação: 2013
Editor/Editora: Springer

Livro na base de dados desde 2013-12-22T19:04:18+00:00 (Lisbon)
Página de detalhes modificada pela última vez em 2024-03-18T15:50:07+00:00 (Lisbon)
Número ISBN/EAN: 9783642726002

Número ISBN - Ortografia alternativa:
3-642-72600-3, 978-3-642-72600-2
Ortografia alternativa e termos de pesquisa relacionados:
Autor do livro: annette leo, doherty, paquet, annett leo, leo per, annette bak, berlin leo
Título do livro: organic syntheses, reactivity chemistry, concepts structure, polyquinane chemistry syntheses and reactions


Dados da editora

Autor: Leo A. Paquette; Annette M. Doherty
Título: Reactivity and Structure: Concepts in Organic Chemistry; Polyquinane Chemistry - Syntheses and Reactions
Editora: Springer; Springer Berlin
230 Páginas
Ano de publicação: 2012-03-06
Berlin; Heidelberg; DE
Impresso / Feito em
Língua: Inglês
53,49 € (DE)
54,99 € (AT)
59,00 CHF (CH)
POD
X, 230 p.

BC; Hardcover, Softcover / Chemie/Organische Chemie; Organische Chemie; Verstehen; Congener; Cycloaddition; Terpene; biosynthesis; chemistry; crystal; crystal structure; development; insecticide; isolation; natural product; reactions; rearrangement; structure; synthesis; Organic Chemistry; BB; EA

I Introduction.- II New Synthetic Developments.- A Annulation Reactions.- B Ring Expansion, Contraction, and Cleavage Processes.- C Pauson-Khand Reaction.- D Photochemical Approaches.- E Rearrangement Routes to Polyquinanes.- F Trapping of 1,3-Diyls.- G Transannular Cyclizations.- III Functional Group Manipulation Within Polyquinanes.- A Reactions Involving Ketonic Substrates.- B Carbocationic Processes.- C Reactions Involving Olefinic Centers.- D Miscellaneous.- IV Physical Data for, and Theoretical Analysis of, Polyquinanes.- A Crystal Structure Data.- B Photoelectron Spectra.- C Molecular Orbital Calculations.- D Miscellaneous.- V Molecules of Theoretical Interest.- A Pentalene.- B Semibullvalenes.- C Syn/anti-Sesquinorbornenes.- D Triquinacenes.- E Tricyclic [10]Annulenes.- F Fenestranes and Related Molecules.- G (D3)-Trishomocubanes and Congeners.- H Peristylanes.- I Chemistry Surrounding Dodecahedrane.- VI Natural Products Chemistry.- A Isolation and Physical Properties.- B Biosynthesis and Chemical Transformations.- VII Synthesis of Nonpolycyclopentanoid Natural Products by Way of Diquinane Intermediates.- A Allamcin.- B Boonein.- C BrefeldinA.- D Dendrobine.- E Forsythide Aglycone Dimethyl Ester.- F Ikarugamycin.- G Iridodial.- H Isoiridomyrmecin.- I Loganin and Analogues.- J Oplopanone.- K Plumericin.- L Trichodiene.- M Udoteatrial.- N Xylomollin.- VIII Synthesis of Diquinane Natural Products.- A Cedranoids.- B The Pentalenolactone Group.- C Quadrone and Terrecyclic Acid.- D Ptychanolide.- E Albene.- F Carbaprostacyclins.- G Ryanodine and the Ryanoid Insecticides.- IX Synthesis of Triquinane Natural Products.- A Linear Triquinanes.- B Angular Triquinanes.- C Propellane Structures.- X References.

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