618 research outputs found
Come «accordare le cetre lascive a’ sacri concenti»: i Fiori celesti di G. B. Andreini
[ITA] Lo studio analizza un manoscritto seicentesco di materia lirico-devozionale, registrato con il titolo di Fiori celesti sotto il nome del famoso attore-autore Giovan Battista Andreini, che nei tardi anni Trenta del secolo avrebbe oπerto in dono al «principe Ippolito Estense» questa breve raccolta poetica, letteralmente raccogliendo non solo importanti motivi tematici e formali tipici del periodo barocco, rintracciabili attraverso mappature intertestuali mirate, ma anche interi componimenti dell’Andreini ripresi da altre sue opere più, o meno, celebri, quali il Teatro celeste e Il Sacrificio. - [ENG] How to «tune lascivious citharas to sacred harmonies»: Fiori celesti by G. B. Andreini ·
This study analyses a 17th-century manuscript containing devotional poems, registered with the title Fiori celesti [Celestial Flowers] to the name of the renowned actor-author Giovan Batti- sta Andreini, who in the late 30s of the 17th century would oπer this short poetry collection to the «prince Ippolito Estense», indeed collecting not only typically baroque thematic and formal Leitmotifs, detectable by careful intertextual mapping, but also full poems derived from other works that Andreini published, more or less famously, such as Celestial Theatre and The Sacrifice
Specchi della Collezione Andreini, nn. 70 e 71
Due specchi etruschi della raccolta Andreini, acquistati nel 1731 da Gian Gastone dei medic
La Ferinda di Giovan Battista Andreini: strategie musicali di un comico dell'arte
il saggio analizza la commedia "La Ferinda" di G. B. Andreini, concepita come interamente musical
I Classici nella Cina antica
e Classics in Ancient China
e study of the reception of the Classics in China offers a compelling
view of how these texts’ meanings have evolved over the centuries, challeng-
ing the notion of a stable and “original”, authentic meaning. e Five Classics
(Wǔjīng 五經), the cornerstone of elite education and the embodiment of
imperial orthodoxy from the 2nd century BCE, have seen their interpretation
and use change profoundly in response to shifting political and socio-cultural
needs. e inseparable link between the classic and its commentary is crucial:
Classics owe their authority to the interpretations that accompany and renew
them. In this context, traditional distinctions between author and exegete,
canon and commentary, often blur, revealing that a literary work’s meaning
arises from an ongoing dialogue between the text and the myriad voices that
reinterpret it over time
Highly diastereoselective synthesis of (E)-1-(trimethylsilyl)-1-en-3-ynes, and (1E,3Z)- and (1E,3E)-1-(trimethylsilyl)-1,3-dienes
In the stereospecific palladium-catalysed cross-coupling reaction of 1-alkynylzinc chlorides or (E)-1-alkenyl diisobutylalanes, (E)-2-bromovinyltrimethylsilane reacts preferentially, in the presence of the corresponding (Z) -stereoisomer to afford good yields of (E)-1-trimethylsilyl-1-en-3-ynes (4) or (1E, 3E)-1-trimethylsilyl -1,3-dienes (6), respectively, having very high stereoisomeric purities. Compounds 4 are easily converted into (1E, 3Z) -1-trimethylsilyl-1,3-dienes (5) by selective hydrometallation reactions, followed by protonolysis
Diastereoselective synthesis of (E)-1-trimethylsilyl-3-en-1-ynes by palladium-catalyzed cross-coupling reaction between trimethylsilylethynylzinc chloride and stereoisomeric mixtures of 1-bromo-1-alkenes
(E)-1-Trimethylsilyl-3-en-1-ynes have been diastereoselectively synthesized starting from stereoisomeric mixtures of 1-bromo-1-alkenes. The procedure has been employed to prepare (2E,6E)-1-acetoxy-2,6-decadien-4-yne, a naturally-occuring acetylenic compound
Palladium-catalyzed diastereoselective syntheses of (E)-1-trimethylsilyl-2-alkenes, (E)-1-trimethylsilyl-1-alken-3-ynes, (1E,5E)-1-trimethylsilyl-1,5-alkadien-3-ynes, (1E,3Z)- and (1E,3E)-1-trimethylsilyl-1,3-alkadienes
On the basis of the observation that (E)-1-bromo-1-alkenes undergo preferentially stereospecific Pd-catalyzed cross-couplings with a variety of organometallics, in the presence of the corresponding (Z)-stereoisomers, efficient and convenient diastereoselective procedures have been developed to prep. nearly stereoisomerically pure (E)-1-trimethylsilyl-2-alkenes, (E)-1-trimethylsilyl-1-alken-3-ynes (I), (1E, 5E)-1-trimethylsilyl-1,5-alkadien-3-ynes (II), and (1E,3E)-1-trimethylsilyl-1,3-alkadienes (III) from stereoisomeric mixts. of alkenyl bromides. Compds. I have been stereoselectively converted into (1E,3Z)-1-trimethylsilyl-1,3-dienes (IV) by selective hydrometallations, followed by hydrolysis. Some synthetic applications of compds. I-IV have been also examd
Journey towards current drama through commedia dell' arte and G. B. Andreini
Current playwriting is performed with awareness that its product, the text, will be performed on stage: therefore it takes into consideration the specific qualities of theatre and it's being percieved as one of its components. It hasn't been always like this, though, until the 20th century drama together with theatre was being classified as undoubtable part of literature. In this thesis I will try to explore why these two different points of view exist and why their exchange occurred. I will examine the changes in the relationship of theatre and literature. I will sketch this question from the origins of theatre in the ancient Greece, through the medieval folk theatre to the baroque commedia dell'arte. In the second part I will focus on the role in the balancing of this relationship that was played by the work of the playwright, the actor and capocomico Giovan Battista Andreini in the turn of the 16th and 17th century. I will analyse the revision performed by this author on this topic on the example of his play Two comedies in one - and I will try to prove the meaningfulness of such revision on the current performance of this play, introduced by the group Geisslers Hofcomoedianten in 2014. In the enclosure there is a brief interview with translator Kateřina Bohadlová, the author of the translation..
DIETETIC AND TOXICOLOGICAL PARAMETERS EVALUATION IN AONYX CINEREUS
Aonyx cinereus is the smallest otter existing, listed as Vulnerable under IUCN red list. Data on diet and nutritional intake of this species in the wild are scarce. Despite this, one of the most important parameters in the management of Aonyx cinereus in captivity, is the development of an appropriate diet program. The diet should meet nutritional needs of animals, guarantee an adequate intake of essential trace elements and be free from non-essential metals that could induce harmful effects. The three subjects included in this study arrived to Maitine Zoo few months ago and are the first specimens hosted in the park. For those reasons, we collected samples of food and faces of otters on weekly basis for 7 weeks, evaluating protein, lipidic and caloric content of the daily food rations of the animals. Moreover, we analysed concentration of trace elements in food and faeces, to define if the diet is balanced and safe and to acquire information about the metabolic processes of clawed otters. This study provides scientific data on Aonyx cinereus nutritional needs, metabolism and possible exposure to detrimental contaminants, giving useful information to implement the welfare and the health status of clawed otters under human care
Palladium-mediated reactions between 1-alkynylzinc chlorides and (E)/(Z)-1,2-dibromoethylene or (E)-1,2-dibromo-1,2-diphenylethylene
(E)/(Z)-1,2-Dibromoethylene (I) underwent palladium-catalyzed diastereoselective alkynylation reaction with alkynylzinc chlorides RC≡CZnCl (R = Bu, BuCH2, Me3Si, Ph, 2-thienyl) to afford bromoenynes (E)-RC≡CCH:CHBr (II) and endiynes RC≡CCH:CHC≡CR (III) with very high stereoisomeric purity. Compds. II and III can be obtained selectively according to the molar ratio between the reagents. Evidence has been obtained that the diastereoselectivity of the alkynylation reactions can be attributed to a diastereoselective oxidative addn. of (E)/(Z)-I to the palladium(0) complex used as catalyst in these reactions. It has also been shown for the 1st time that the complexes which derive from the oxidative addn. of (E)-I or (E)-1,2-dibromo-1,2-diphenylethylene (IV) to Pd(PPh3)4 easily undergo decompn. affording both PdBr2(PPh3)2 and acetylene or diphenylacetylene, resp. Finally, it has been shown that the reaction of IV with organozinc derivs., in the presence of catalytic amts. of Pd(PPh3)4, affords diphenylacetylene, selectively, instead of cross-coupling products
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