Campher

Camphor was isolated from camphor tree oil by by fractional destillation and recrystallized from ethanol. The UV‐, CD‐, IR‐ NMR‐ und MS‐spectra were recorded and are reproduced in the supplementary material. The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the 13C chemical shifts. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Colchicin

Colchicin was extracted from grinded seeds of meadow saffron and purified by flash chromatography and preparative HPLC. All analytical spectra were recorded and are reproduced either in the main part or in the supporting information. The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the ¹³C chemical shifts. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Thymochinon – das Gelbe vom Öl

Thymoquinone has been obtained by steam distillation from the yellow cold pressed oil of the seeds of Nigella sativa L. and purified by column chromatography. All analytical spectra were recorded and are reproduced either in the main part or in the supporting information. The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the ¹³C chemical shifts. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Raffinose + Raffinase = Raffinade: Raffiniert!

Raffinose has been obtained by extraction with 50% ethanol from the seeds of the Sweet Blue Lupine and purified first via a Cation exchange column and finally by analytical HPLC using a RI‐detector. All analytical spectra were recorded and are reproduced either in the main part or in the supporting information. The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the ¹³C chemical shifts. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Sinensetin

Sinensetin was isolated from cold pressed orange peel oil and recrystallized from ethanol. All analytical spectra were recorded and are reproduced either in the main part or in the supporting information (www.chiuz.de). The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the ¹³C chemical shifts. The project is a follow up of the book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Eucalyptol aus Eukalyptusöl

Eucalyptol (1,8‐cineol), a cyclic monoterpenoid ether, is the dominant portion of eucalyptus oil, an essential oil of Eucalyptus globulus, accessible by steam distillation of its leaves. Some herbs and spices such as basil and cardamom also contain it as characterising flavour compound. Eucalyptus is a very diverse genus of Myrtaceae naturally occurring in Australia to whom the species have adapted in evolution. Planting Eucalyptus trees outside Australia has both benefits for poor populations and drawbacks. Especially, the enormous water consumption has been criticized. The total impact is doubtful. Eucalyptol is used in flavorings, fragrances, confectionery, cosmetics, cough suppressants, and insect repellents. Higher than normal doses are a hazard. A convenient isolation of eucalyptol from eucalyptus is reported. All analytical spectra were recorded and are reproduced and interpreted either in the main part or in the supporting information. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Kokain

Cocaine was isolated from dried tea leaves and chromatographically purified by HPLC. The UV‐, CD‐, IR‐ NMR‐ und MS‐spectra are reproduced in the supplementary material. The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the ¹³C chemical shifts. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Vom Granatapfelbaum zum Cyclooctatetraen

The alkaloid pseudopelletierine is, together with pelletierine and N‐methylpelletierine, deposited in the bark of the pomegranate tree. Whereas pelletierine and the N‐methylpelletierine were used a long while as vermifuges, pseudepelletierine gained historical interest as starting product of the first cyclooctatetraene synthesis. We describe its isolation from cortex punica granatum and the full set of its analytical spectra. The NMR spectra and the EI‐mass spectrum are discussed in detail and the ¹³C‐chemical shifts compared with the theoretically derived data.     

Friedelin aus Kork

Cork of the cork oak is a fascinating natural material, used since ancient times. According to a close sight at cork, in 1665 the term “cell” was coined for use in biology. Friedelin, a complex pentacyclic triterpene ketone, is a constituent of cork. The isolation of friedeline is described as well as its history. All analytical spectra were recorded and are reproduced either in the main part or in the supporting information. The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the ¹³C chemical shifts. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Diosgenin aus Yams als Hormonvorstufe

Diosgenin as a sapogenin is the aglycone of the saponine dioscin. It is occuring in plants such as yam, from which it is isolated on industrial scale since the 1940ies. Plant diosgenin is a starting substance for the synthesis of human, i.e. animal, hormones and “the pill”, which as a hormonal contraception represents a revolution in the control of human sexuality. History, isolation and spectroscopy of this complex sapogenin are reported. This article extends the briskly discussed feature “50 years pill in Germany” (Streller & Roth, ChiuZ, 2011 [( 1 ) ]) by a particular compound example. It belongs to the series on isolation and spectroscopy of natural products in this journal.     

Scharf,schärfer,Capsaicin!

Capsaicin, the spiciest hot compound known, is a non‐basic alkaloid of chili peppers, belonging to the genus Capsicum. With 16 million units it is on top of the Scoville scale, a measure for the degree of spicy heat within a food. Capsicum, capsaicin and this scale have already been discussed in this journal in 2010. After botanical and culinary aspects, now a method for the separation of the main capsaicinoids, capsaicin and dihydrocapsaicin, is reported which makes use of the complexation of capsaicin by Ag+ ions on an AgNO₃ impregnated silica gel column. All analytical spectra were recorded. They are reproduced either in the main part or in the supporting information and discussed in detail. Calculations of the structure are compared with data of an own x‐ray analysis of capsaicin. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Karminsäure

Carminic acid was isolated from dried Dactylopius coccus Costa (Dactylopiidae) and chromatographically purified. All analytical spectra were recorded and are reproduced either in the main part or in the supplementary material. The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the ¹³C chemical shifts. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Über Rosmarin und Rosmarinsäure

Rosmarinic acid, a tan from Lamiaceae, is found in rosemary and many other plants such as thyme, painted nettle, savory, sage, oregano, or lemon balm, from which it has been isolated here. It is a caffeic acid ester and a chiral, aromatic natural product. Rosmarinic acid tastes bitter, which may be attractive for rosemary as spice. Due to the catechol subunit the acid is an antioxidant. Using rosmarinic acid as a cure is possible due to manyfold physiological effects which are still under investigation. The rosmarinic acid biosynthesis pathway was completely elucidated at the painted nettle. This led to attempts to produce the acid biotechnologically by plant cell cultures in high yields. The preparation of a spectroscopically pure sample is challenging. All analytical spectra were recorded and are reproduced and interpreted either in the main part or in the supporting information.     

Die optischen Aufheller Fraxin und Aesculin

The closely related glycosides fraxin and esculin have been isolated in pure form from an ash bark extract by gel permeation chromatography. This challenging separation is a prime example for the preparative value of a crosslinked dextran gel. Silicagel 60 only leads to pure esculin. The terms optical brighteners and fluorescence are discussed. All analytical spectra were recorded and are reproduced and interpreted either in the main part or in the supporting information. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Ein Wirkstoff gegen Malaria aus der Natur: Artemisinin

Artemisinin, an unusual tetracyclic, endoperoxidic sesquiterpene is a highly bioactive natural product. Due to its superior activity against the malaria parasite it is under investigation to an extraordinary extent. The Chinese scientist Tu Youyou who discovered the compound received the Nobel Prize for medicine 2015. However, treating malaria is not all of its potential. This paper is following up two recent articles on artemisinin in this Journal from 2014. We describe here the isolation of pure crystalline artemisinin from dried sweet wormwood leaves and present its complete set of spectra together with interpretations. Background information complements the matter.     

Steviosid aus Süßkraut

The diterpene glycoside stevioside is the most abundant among a group of sweet steviol glycosides, present in sweetleaf (Stevia rebaudiana), which is naturally occurring in Paraguay. It has already been used by the Guarani Indians as a sweetener. Since 2011 such “steviosides” have an EU approval as sweeteners E 960. They taste ca. 250 times sweeter than sucrose. Meanwhile, they have got a significant recognition, not least due to their use in Coca Cola life®. We describe the isolation of stevioside and rebaudioside A from dried leaves of the sweetleaf plant. The complete set of spectra for stevioside is reported. Based on students' laboratory work this project is a follow up of the book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Chlorophyll

Chlorophyll exists since ca. 3 billion years and is at begin of the evolution. This chiral, green Mg‐porphyrin‐complex absorbs as a photosensitizer in the antennas of the light‐harvesting complexes of chloroplasts all parts of visible light except of green light. This energy is transferred to the reaction centres of oxygenic photosynthesis. By this redox reaction carbon dioxide and water are transformed into carbohydrates and oxygen. We describe how the structures of chlorophylls were elucidated, discuss structure‐property relations, the relationship to heme of blood, everyday uses, and how Green has influenced our language. The isolation of pure chlorophyll a from spinach is an experimental challenge, which we report in detail. All analytical spectra were recorded and are reproduced and interpreted either in the main part or in the supporting information.     

Mit der Eberesche vom Heimatlied zur Frühstücksmagarine

The mountain ash (rowan tree) belongs to the adaptable trees of pioneer vegetation. Its fruits are edible and can be used for dishes and beverages. Appropriate knowledge is, however, required to avoid dissapointments. Their use in folk medicine is also known. In the German Ore Mountain region there is a special folk song as a song of praise for the tree. Typical chemical ingredients are the constituents parasorboside ( 1 ), a glucoside, parasorbinic acid ( 2 ), a lactone, and sorbinic acid ( 3 ), an unsaturated carboxylic acid. It is chemically accessible from 2 and used as a preservative. In more than 100 years, the structures were determined by renowned chemists. The access to 1 , 2 , and 3 based on the mountain‐ash rowan berries is described. All analytical spectra were recorded and are reproduced and interpreted either in the main part or in the supporting information.     

Eine Boswelliasäure aus Weihrauch

3‐O‐Acetyl‐11‐keto‐β‐boswelliasäure was extracted from pulverized frankincense and purified by HPLC. All analytical spectra were recorded and are reproduced either in the main part or in the supporting information. The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the ¹³C chemical shifts. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).     

Wie unsere Nase die enantiomeren Linaloole unterscheidet

Both enantiomeric forms of Linalool have been obtained by vacuum distillation from the oils of Rosewood or Coriander. Subsequently they have been purified by column chromatography. All analytical spectra were recorded and are reproduced either in the main part or in the supporting information. The NMR‐ and mass‐spectra have been interpreted and compared with theoretical calculations of the ¹³C chemical shifts. The project is a follow up of the recent book “Classics in Spectroscopy” by S. Berger und D. Sicker (Wiley‐VCH 2009).