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Record Nr. |
UNINA9910785761703321 |
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Autore |
Wellman Judith |
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Titolo |
The road to Seneca Falls [[electronic resource] ] : Elizabeth Cady Stanton and the First Woman's Rights Convention / / Judith Wellman |
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Pubbl/distr/stampa |
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Urbana, : University of Illinois Press, c2004 |
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ISBN |
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1-283-58351-8 |
9786613895967 |
0-252-09282-1 |
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Descrizione fisica |
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1 online resource (317 p.) |
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Collana |
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Women in American history |
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Disciplina |
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Soggetti |
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Feminists - United States |
Women's rights - New York (State) - Seneca Falls - History |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Includes bibliographical references (p. [241]-286) and index. |
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Nota di contenuto |
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Part 1. The context : converging paths -- Elizabeth Cady Stanton : growing up, 1815-35 -- Entering the world of reform : antislavery and women's rights, 1835-40 -- Communities in transition : Seneca Falls and Waterloo, 1795-1840 -- Part 2. The movements : parallel paths -- Minding the light : Quaker traditions in a changing world -- Seneca Falls : abolitionist ferment -- Women and legal reform in New York State -- Part 3. Converging paths : the event -- Adversity and transcendence, June 1847-June 1848 -- Declaring women's rights, July 1848 -- The road from Seneca Falls, 1848-1982. |
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2. |
Record Nr. |
UNINA9910557494003321 |
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Autore |
Nishiwaki Nagatoshi |
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Titolo |
Nitro Compounds and Their Derivatives in Organic Synthesis |
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Pubbl/distr/stampa |
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Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
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Descrizione fisica |
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1 online resource (120 p.) |
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Soggetti |
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Research & information: general |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Sommario/riassunto |
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Nitro chemistry plays an important role in organic synthesis to construct new frameworks. This is due to the diverse properties of the nitro group. The strong electron-withdrawing ability of the nitro group reduces the electron density of the scaffold, facilitating reactions with nucleophiles or electron transfer. In addition, the -hydrogen of the nitro group is highly acidic, giving a stable anion, which facilitates reactions with both electrophilic and nucleophilic reagents. In addition, the nitro group also serves as a good leaving group, which facilitates transformation to a wide variety of functional groups. Despite the substantial contributions of many researchers, nitro chemistry is still an exciting and challenging research area. This book brings together recent original research and review articles contributed by an international team of leading experts and pioneers in organic synthesis using nitro groups. It is sure to provide useful information and promising insights for researchers. |
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