Grand Designs: Synthesis

Reactions ◽  
2011 ◽  
Author(s):  
Peter Atkins

In this final reaction I am going to show you in the broadest of outlines how chemists build the equivalent of a cathedral. That is, how they synthesize a complicated molecule from scratch. The aim of a synthesis is to take a reasonably readily available laboratory chemical and process it—add bits on, take things off, close rings of atoms, open rings, build flying buttresses, and so on—until the target compound has been made. You could take the view that you should really start from absolute scratch, from the elements themselves, typically hydrogen, carbon, nitrogen, and oxygen, and build the molecule from those. However, that would be a waste of time and not crucial to the demonstration of the synthetic route because it is possible to argue that there are already plenty of methods for synthesizing the simple starting materials from scratch, and the real challenge is to build the intricate molecule. That is rather like accepting that a contractor can supply windows, bricks, and beams when constructing a real house and that it isn’t necessary to go all the way back to the sand, clay, and iron ore from which they are made to demonstrate that the house can be built literally from the ground up. Of course, the starting materials in a modern chemical synthesis might seem a bit recondite, but be assured that they are reasonably acceptable and purchasable from suppliers of laboratory reagents or easily made from what they do supply. Now for the particular cathedral on which I intend to focus. That scourge of humanity, malaria (‘bad air’), was introduced into the New World in the fifteenth century and soon wrought the havoc that had for long, and still, afflicts millions. The natives there found that an extract of the bark of the quina-quina tree, in due course to be classified as Cinchona Officinalis, was an effective cure, in particular having saved the life of the Countess of Cinchona. In due course the active component, quinine, was identified and extracted.

1981 ◽  
Vol 1 (1) ◽  
pp. 48-57
Author(s):  
Olle af Geijerstam ◽  
Jim Cordts
Keyword(s):  
Iron Ore ◽  

2018 ◽  
Vol 36 (2) ◽  
pp. 355-381 ◽  
Author(s):  
James Muldoon

Historians have argued that sixteenth and seventeenth century English colonial charters claimed the lands of indigenous people on the basis of their discovery by Europeans. Examination of these charters, however, demonstrates that a charter authorized acquiring land from the indigenous population in a specific region, not seizing indigenous it, and regulating the entry of other potential settlers. Charters also regulated overseas relations among the European nations to reduce or prevent international conflict by recognizing similar claims to monopoly of access to lands claimed by other developing empires. Charters were rooted in a medieval legal tradition that included canon law commentaries that recognized the legitimacy of infidel dominium and papal bulls that sought to regulate fifteenth-century Iberian expansion in the Atlantic. English charters built on this legal tradition and were a stage in the creation of a European legal order for overseas expansion. The fundamental issue was regulation of the sea and sea routes to Asia and to the New World, not the acquisition and possession of indigenous land. The English charters should be understood as elements of the long-running debate about whether access to the sea was open to all or could be closed to outsiders.


2012 ◽  
Vol 18 (7) ◽  
pp. 428-436 ◽  
Author(s):  
Stephen Kent ◽  
Youhei Sohma ◽  
Suhuai Liu ◽  
Duhee Bang ◽  
Brad Pentelute ◽  
...  

Author(s):  
Erica Maier

European expansion in the New World during the fifteenth century created inter-­‐ethnic households and relationships, which led to the creation of newly creolised and distinct cultures. Inter-­‐ethinic relationships also lead to retention of culture, for both First Nations peoples and Europeans as well. Specifically focusing on Russian and Spanish settlements in North America, this paper examines creolisation by studying the household archaeologically to determine the daily activities of creole cultures, First Nations peoples, and European settlers. 


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mayte Green-Mercado

Abstract Late medieval and early modern diplomats and intermediaries drew on the authoritative language of prophecy, a language that conveyed divine threats to the current order, or divine sanctions of a new world. Because apocalyptic discourse has the capacity to conjure affective associations through its redemptive potential, its use in a diplomatic context seems to have been aimed at shaping the way individuals perceived the issues at hand. Based on a number of case studies from both Christian and Islamic contexts, this contribution renders it clear that it was precisely these cultural and political commonalities that made prophecy a recognizable political and diplomatic discourse. As a totalizing religio-political discourse, prophecy articulated the aspirations of a multitude of competing universalizing imperial projects that were emerging in the fifteenth century, which required diplomatic mediation.


Nanoscale ◽  
2021 ◽  
Author(s):  
Mariya A. Zvaigzne ◽  
Pavel Samokhvalov ◽  
Yurii Gun'ko ◽  
Igor Nabiev

The production of enantiopure chemicals is an essential part of modern chemical industry. Hence, the emergence of asymmetric catalysis led to dramatic changes in the procedures of chemical synthesis, and...


1987 ◽  
Vol 18 (3) ◽  
pp. 263-276
Author(s):  
Michael E. Williams

NOT FAR from Cadiz there is an English property that has remained Catholic for close on five hundred years. Its history goes back to pre-reformation days, indeed to the thirteenth century when the port of Sanlucar de Barrameda was recaptured from the Moors by the Guzman family who later became the Dukes of Medina Sidonia. Strategically Sanlucar was an important port because it was at the mouth of the Guadalquivir and as well as capturing the Seville trade it also commanded the traffic from the Mediterranean to Northern Europe and eventually it was the point of departure for ships leaving for the New World. Among the various nations using the port the English were conspicuous and their merchants were granted various privileges by the Dukes of Medina Sidonia during the fifteenth century. By the early sixteenth century there is evidence of a sizeable colony in the town; in fact the English were the largest single group of foreigners and many English names appear in the baptismal registers as both parents and godparents. At least one of them held high public office in the town. On the accession of Henry VIII to the throne of England, the situation further improved as he abandoned the neutrality of his father and allied himself with Spain against France. So it was that in 1517 a new charter of privileges for the English merchants in Sanlucar was drafted. A grant of land by the river was made so as to provide a chapel and a burial place for Englishmen. The chapel was dedicated to St. George and it was to be looked after by a confraternity. The chaplain was to be appointed by the Bishops of London, Winchester and Exeter, since it was from these dioceses that most of the merchants came. Although there have been rebuildings, this site has remained English ever since.


2019 ◽  
Vol 43 (11-12) ◽  
pp. 480-485
Author(s):  
Caijiao Wu ◽  
Qifan Zhou ◽  
Dake Song ◽  
Hui Li ◽  
Changshun Bao ◽  
...  

A practical synthetic route to pimavanserin tartrate, in which the target compound was obtained with 99.84% purity and in 46% total yield via a 5-step synthesis starting from 4-hydroxybenzaldehyde and (4-fluorophenyl)methanamine, is reported. The main advantages of the route include inexpensive starting materials, mild reaction conditions and an acceptable overall yield.


2018 ◽  
Vol 14 ◽  
pp. 856-860 ◽  
Author(s):  
Bettina Riedl ◽  
Walther Schmid

Synthetic approaches towards N-acetylgalactosamine (GalNAc) have been attracting considerable interest since this compound is known for its pivotal role in cell–cell interaction and receptor induced cell signaling. Herein, we present a synthetic route in which two of the four stereogenic centers present in the target compound are derived from enantiopure tartaric acid being selectively converted to epoxy alcohols. The key step is the Pd-catalyzed, stereo- and regioselective epoxide opening and subsequent nucleophilic substitution of an azide functionality. This approach enables the synthesis of the naturally D- and unnaturally L-configured GalNAc, as well as both enantiomers of the largely unknown N-acetylidosamine (IdoNAc).


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