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Terpenes

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Terpenes is the generic term summarizing all kinds of isoprene polymers and their derivatives with its general formula of (C5H8) n. Terpene is a class of compound that is ubiquitous in the plant kingdom, but exist in very few amount in the animal kingdom. Except in the form of terpene hydrocarbons, there are a large number of terpenes forming various kinds of oxygenated derivatives including alcohols, aldehydes, ketones, carboxylic acids, esters and glycoside forms. Secondly there are also nitrogen-containing derivatives as well as a minority of sulfur-containing derivatives presented. Based on the number of the isoprene units contained inside the molecule, the terpenes can be divided into: monoterpene, sesquiterpenoid, diterpene, sesquiterpene, triterpenoids, tetraterpene and polyterpene.

For some compound which originated from the synthesis of isoprene, but has the number of carbon atoms in the molecule be not an integer multiple of 5, they are called terpenoid. In the life activities, terpenoids compound, especially inside the plants, have important functions, for example gibberellin, abscisic acid and insect juvenile hormone are important hormones, carotenoids and chlorophyll are important photosynthetic pigments; plastoquinone and quinone are respectively important electronic chain delivery body in photosynthesis and respiration chain; sterols are the component of the biological membrane.

Monoterpene and sesquiterpene are the major component of volatile oil. Diterpene is the major substance forming the resin; triterpenoid is an important material forming plant saponins and resins, tetraterpene mainly include some fat-soluble pigments widely distributed in the plants. In nature, terpenoids is widely distributed, some of which have physiological activity. For example, ascaridole and santonin have roundworm expelling effect; artemisinin has antimalarial effect while andrographolidume has antibacterial effect.

The following describes some of the chemical reactions associated with terpenes. This is significant for determination of the chemical structure of terpene component.

(1) Oxidation reaction
Different oxidants, in different situations, can oxidize the different groups contained in terpene component to produce different products. For example, chromic acid can oxidize the carbon methyl group and gem-dimethyl carbon to produce acetic acid; the oxidation reaction of ozone is a valuable double bond cleavage reaction and can determine the position of double bond in the structure of the terpene composition. Lead tetraacetate is also oxidation agents of double-bond and has been widely used in chemical research of the terpene ingredients.

(2) The dehydrogenation
Dehydrogenation reaction can be considered as a kind of oxidation reactions and is a kind of valuable reaction for the study the chemical structure of terpenes particularly cyclic terpene. It refers to that the terpene component is heated (200 ℃ ~ 300 ℃) together with sulfur or selenium under an inert atmosphere, the carbon skeleton of the cyclic terpene is dehydrogenated into aromatic derivatives with sometimes the ring being cleaved and sometimes cyclization occurring simultaneously.

(3) Addition reaction
The double bonds in the terpene components can react with hydrogen halide acids such as hydroiodic acid or hydrogen chloride in glacial acetic acid solution to generate crystalline-shaped addition product. It can also absorb bromine (diethyl ether or glacial acetic acid - ethanol solution) to generate bromide with certain physicochemical properties. If mixing the glacial acetic acid and sodium nitrite for shaking, nitrous oxide or pseudo-nitrous oxide will be generate and will exhibit visible special colors.
If the unsaturated terpene component was added with amyl nitrite and concentrated hydrochloric acid for mixing with shaking and keep it cool, then add a small amount of ethanol or glacial acetic acid, there will be chlorinated nitroso derivative of terpenes generated with special colors as well. Such nitroso derivatives (including nitrous oxides and chlorinated nitroso derivative) mostly exhibit blue or blue-green color. They are easily polymerized to form a colorless di-polymer, but when the di-polymer is heated to a molten state or when made into a solution, it can also be converted into a blue or blue-green single-molecule compound.
Nitroso chlorinated derivatives can condense with primary or secondary amines (commonly piperidine) to generate nitroso amines with most of them having complete crystal shape and  certain physical and chemical constants available for the identification of unsaturated terpene components. If the terpene component molecules contain conjugated double bonds, then it will form crystalline addition product with maleic anhydride through Diels-Alder reaction which can be used to prove the presence of conjugated double bonds.

(4) Wagner-Meerweein rearrangement;
Terpene molecules, sometimes through the effect of agents (such as acid, etc.), the carbon skeleton can be changed or the functional groups in the molecule can be transferred in the molecule. Especially during the elimination reaction, addition reaction or a nucleophilic substitution reaction of bicyclic terpene compound, there is often Wagner-Meerweein rearrangement happening.

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Structure:
Chemical Name:
FITONE
CAS:
502-69-2
MF:
C18H36O
Structure:
Chemical Name:
CIMIGENOL 3-O-BETA-D-XYLOPYRANOSIDE
CAS:
27994-11-2
MF:
C35H56O9
Structure:
Chemical Name:
Ganodermenonol
CAS:
104700-97-2
MF:
C30H46O2
Structure:
Chemical Name:
ALPHA-ONOCERIN
CAS:
511-01-3
MF:
C30H50O2
Structure:
Chemical Name:
ailanthone
CAS:
981-15-7
MF:
C20H24O7
Structure:
Chemical Name:
artemisic acid
CAS:
80286-58-4
MF:
C15H22O2
Structure:
Chemical Name:
DESACETYLNIMBIN
CAS:
18609-16-0
MF:
C28H34O8
Structure:
Chemical Name:
alpha-Amyrenyl acetate
CAS:
863-76-3
MF:
C32H52O2
Structure:
Chemical Name:
(4aS,6aS,6aR,8aR,12aS,14aS,14bS)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4 a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one
CAS:
514-07-8
MF:
C30H48O
Structure:
Chemical Name:
3-Oxo-olean-12-en-28-oic acid
CAS:
17990-42-0
MF:
C30H46O3
Structure:
Chemical Name:
1-(4-Isopropyl-1-methyl-4-pentenyl)-3a,6,6,12a-tetramethyltetradecahyd ro-1H-cyclopenta[a]cyclopropa[e]phenanthren-7-yl acetate
CAS:
1259-94-5
MF:
C33H54O2
Structure:
Chemical Name:
[(3S,4aS,6aR,6bS,8aR,12aR,14aS,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl -1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate
CAS:
1616-93-9
MF:
C32H52O2
Structure:
Chemical Name:
6β,16-Dihydroxykauran-2β-yl β-D-glucopyranoside
CAS:
53452-34-9
MF:
C26H44O8
Structure:
Chemical Name:
Rutundic acid
CAS:
20137-37-5
MF:
C30H48O5
Structure:
Chemical Name:
4-Hydroxy-2,6,6-trimethyl-1-cyclohexenecarboxylic acid
CAS:
62218-55-7
MF:
C10H16O3
Structure:
Chemical Name:
(13α,14β,17α,20S,23R,24S)-21,24-Epoxy-23,25-dihydroxy-5α-lanost-7-en-3-one
CAS:
6985-35-9
MF:
C30H48O4
Structure:
Chemical Name:
D:B-Friedo-B':A'-neogammacer-5-en-3β-ol
CAS:
1615-94-7
MF:
C30H50O
Structure:
Chemical Name:
13-Hydroxy-8,11,13-podocarpatrien-18-oic acid
CAS:
61597-83-9
MF:
C17H22O3
Structure:
Chemical Name:
2α,3α,24-Trihydroxyurs-12-en-28-oic acid
CAS:
89786-83-4
MF:
C30H48O5
Structure:
Chemical Name:
Gadermandiol
CAS:
107900-76-5
MF:
C30H48O3
Structure:
Chemical Name:
PIMARIC ACID
CAS:
127-27-5
MF:
C20H30O2
Structure:
Chemical Name:
WILFORGINE
CAS:
37239-47-7
MF:
C41H47NO19
Structure:
Chemical Name:
28-deoxonimbolide
CAS:
126005-94-5
MF:
C27H32O6
Structure:
Chemical Name:
rosenonolactone
CAS:
508-71-4
MF:
C20H28O3
Structure:
Chemical Name:
xanthatin
CAS:
26791-73-1
MF:
C15H18O3
Structure:
Chemical Name:
3-Epikatonic acid
CAS:
76035-62-6
MF:
C30H48O3
Structure:
Chemical Name:
Phytolaccagenin
CAS:
1802-12-6
MF:
C31H48O7
Structure:
Chemical Name:
(23S)-17,23-Epoxy-29-hydroxy-27-nor-5α-lanost-8-ene-3,24-dione
CAS:
81678-46-8
MF:
C29H44O4
Structure:
Chemical Name:
Hop-17(21)-en-3β-ol
CAS:
564-14-7
MF:
C30H50O
Structure:
Chemical Name:
3-Methyl-2-butenoic acid [2-[5-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-6-oxo-7-(2-oxopropyl)-4-cyclohepten-1-yl]vinyl] ester
CAS:
74690-89-4
MF:
C25H36O5
Structure:
Chemical Name:
(4aR)-5β-[2-(3-Furyl)ethyl]-3,4,4aβ,5,6,7,8,8a-octahydro-5,6α,8aα-trimethyl-1-naphthalenecarboxylic acid
CAS:
1782-65-6
MF:
C20H28O3
Structure:
Chemical Name:
12-Hydroxy-8(17),13-labdadien-16,15-olide
CAS:
958885-86-4
MF:
C20H30O3
Structure:
Chemical Name:
15,18-Dihydroxyabieta-8,11,13-trien-7-one
CAS:
213329-45-4
MF:
C20H28O3
Structure:
Chemical Name:
20,24-Epoxy-24-methoxy-23(24-25)abeo-dammaran-3-one
CAS:
1020074-97-8
MF:
C31H52O3
Structure:
Chemical Name:
3-Acetoxy-27-hydroxy-20(29)-lupen -28-oic acid methyl ester
CAS:
263844-80-0
MF:
C33H52O5
Structure:
Chemical Name:
3-O-Acetyloleanderolide
CAS:
62498-83-3
MF:
C32H50O5
Structure:
Chemical Name:
Cabraleahydroxylactone
CAS:
35833-69-3
MF:
C27H44O3
Structure:
Chemical Name:
Celaphal A
CAS:
244204-40-8
MF:
C17H20O4
Structure:
Chemical Name:
Coronarin D ethyl ether
CAS:
138965-89-6
MF:
C22H34O3
Structure:
Chemical Name:
Echiphyllin C
CAS:
310433-44-4
MF:
C20H29NO3
Structure:
Chemical Name:
ent-14,16-Epoxy-8-pimarene-3,15-diol
CAS:
1188281-98-2
MF:
C20H32O3
Structure:
Chemical Name:
Eriocalyxin B
CAS:
84745-95-9
MF:
C20H24O5
Structure:
Chemical Name:
Hythiemoside A
CAS:
853267-91-1
MF:
C28H46O9
Structure:
Chemical Name:
Methyl eichlerianate
CAS:
56421-12-6
MF:
C31H52O4
Structure:
Chemical Name:
Myriceric acid B
CAS:
55497-79-5
MF:
C39H54O7
Structure:
Chemical Name:
Pre-schisanartanin B
CAS:
1033288-92-4
MF:
C31H42O11
Structure:
Chemical Name:
SOYASAPOGENOL B(P)
CAS:
595-15-3
MF:
C30H50O3
Structure:
Chemical Name:
grandifloric acid
CAS:
22338-69-8
MF:
C20H30O3
Structure:
Chemical Name:
moronic acid
CAS:
6713-27-5
MF:
C30H46O3
Structure:
Chemical Name:
actinidic acid
CAS:
341971-45-7
MF:
C30H46O5
Structure:
Chemical Name:
taxinine M
CAS:
135730-55-1
MF:
C35H42O14
Structure:
Chemical Name:
steviolbioside
CAS:
41093-60-1
MF:
C32H50O13
Structure:
Chemical Name:
Carabrone
CAS:
1748-81-8
MF:
C15H20O3
Structure:
Chemical Name:
10-DEACETYL-7-XYLOSYLPACLITAXEL
CAS:
90332-65-3
MF:
C49H63NO17
Structure:
Chemical Name:
Arteannuin
CAS:
50906-56-4
MF:
C15H20O3
Structure:
Chemical Name:
isocupressic acid
CAS:
1909-91-7
MF:
C20H32O3
Structure:
Chemical Name:
taraxerol
CAS:
127-22-0
MF:
C30H50O
Structure:
Chemical Name:
D-Friedoolean-14-ene-3β,28-diol
CAS:
17884-88-7
MF:
C30H50O2
Structure:
Chemical Name:
(1R,8S)-1α-(3-Furanyl)-6,7,8,9-tetrahydro-8α-[(2,5-dihydro-2-oxofuran)-3-yl]naphtho[1,2-c]furan-3(1H)-one
CAS:
126724-95-6
MF:
C20H16O5
Structure:
Chemical Name:
16-Kaurene-2,6,15-triol
CAS:
53452-32-7
MF:
C20H32O3
Structure:
Chemical Name:
6-Deoxy-9alpha-hydroxycedrodorin
CAS:
247036-52-8
MF:
C27H34O9
Structure:
Chemical Name:
Dihydroniloticin
CAS:
115334-05-9
MF:
C30H50O3
Structure:
Chemical Name:
ent-9-Hydroxy-15-oxo-16-kauren- 19-oic acid beta-D-glucopyrasyl ester
CAS:
81263-96-9
MF:
C26H38O9
Structure:
Chemical Name:
Eucamalol
CAS:
145544-91-8
MF:
C10H16O2
Structure:
Chemical Name:
Itol A
CAS:
1033747-78-2
MF:
C20H32O6
Structure:
Chemical Name:
Micraic acid A
CAS:
659738-08-6
MF:
C22H32O3
Structure:
Chemical Name:
Olean-12-ene-3,24-diol
CAS:
119318-15-9
MF:
C30H50O2
Structure:
Chemical Name:
Pseudolaric acid D
CAS:
115028-67-6
MF:
C20H30O3
Structure:
Chemical Name:
Scutellaric acid
CAS:
102919-76-6
MF:
C30H48O4
Structure:
Chemical Name:
Wilforol C
CAS:
168254-95-3
MF:
C30H48O4
Structure:
Chemical Name:
3,4-Secocucurbita-4,24-diene-3,26,29-trioic acid
CAS:
329975-47-5
MF:
C30H46O6
Structure:
Chemical Name:
(24S)-Cycloartane-3,24,25-triol 24,25-acetonide
CAS:
57576-31-5
MF:
C33H56O3
Structure:
Chemical Name:
14-Deoxy-11-hydroxyandrographolide
CAS:
160242-09-1
MF:
C20H30O5
Structure:
Chemical Name:
2-Oxokolavelool
CAS:
221466-41-7
MF:
C20H32O2
Structure:
Chemical Name:
3,19-Dihydroxy-6,23-dioxo-12-ursen-28-oic acid
CAS:
261768-88-1
MF:
C30H44O6
Structure:
Chemical Name:
CaMaric acid
CAS:
146450-83-1
MF:
C35H52O6
Structure:
Chemical Name:
PoMolic acid 28-O-beta-D-glucopyranosyl ester
CAS:
83725-24-0
MF:
C36H58O9
Structure:
Chemical Name:
Scutebarbatine X
CAS:
1312716-26-9
MF:
C34H38N2O10
Structure:
Chemical Name:
Uncinatone
CAS:
99624-92-7
MF:
C20H22O4
Structure:
Chemical Name:
β-AMyrenonol acetate
CAS:
5356-56-9
MF:
C32H50O3
Structure:
Chemical Name:
DACRENE
CAS:
20070-61-5
MF:
C20H32
Structure:
Chemical Name:
(2S)-2β-(3-Furyl)-4aα,5,6aβ,7,10,11,11aα,11b-octahydro-11bβ-methyl-7β,10β-methano-2H-pyrano[4,3-g][3]benzoxepine-4,6,8(1H)-trione
CAS:
66756-57-8
MF:
C19H20O6
Structure:
Chemical Name:
Rosthornin B
CAS:
125181-21-7
MF:
C24H34O7
Structure:
Chemical Name:
Tereticornate A
CAS:
149751-81-5
MF:
C40H54O6
Structure:
Chemical Name:
Villosin
CAS:
160598-92-5
MF:
C20H28O2
Structure:
Chemical Name:
2,5,14-Triacetoxy-3-benzoyloxy-8,15-dihydroxy-7-isobutyroyloxy-9-nicotinoyloxyjatropha-6(17),11E-diene
CAS:
210108-87-5
MF:
C43H53NO14
Structure:
Chemical Name:
Andropanolide
CAS:
869807-57-8
MF:
C20H30O5
Structure:
Chemical Name:
GANODERIC ACID DM
CAS:
173075-45-1
MF:
C30H44O4
Structure:
Chemical Name:
(13E)-15-Hydroxy-8(17),13-labdadiene-19-al
CAS:
3650-31-5
MF:
C20H32O2
Structure:
Chemical Name:
6-Epidemethylesquirolin D
CAS:
165074-00-0
MF:
C20H28O5
Structure:
Chemical Name:
Bauerel acetate
CAS:
17020-04-1
MF:
C32H52O2
Structure:
Chemical Name:
Clerodermic acid methyl ester
CAS:
67650-47-9
MF:
C21H30O4
Structure:
Chemical Name:
Cycloartane-3,24,25-triol
CAS:
57576-29-1
MF:
C30H52O3
Structure:
Chemical Name:
Diosbulbin J
CAS:
1187951-06-9
MF:
C19H22O8
Structure:
Chemical Name:
ent-3-Oxokauran-17-oic acid
CAS:
151561-88-5
MF:
C20H30O3
Structure:
Chemical Name:
ent-9-Hydroxy-15-oxo-19-kauraic acid
CAS:
77658-45-8
MF:
C20H30O4
Structure:
Chemical Name:
Glaucin B
CAS:
115458-73-6
MF:
C28H32O10
Structure:
Chemical Name:
Heudelotine
CAS:
133453-58-4
MF:
C18H20O2
Structure:
Chemical Name:
Jangomolide
CAS:
93767-25-0
MF:
C26H28O8
Structure:
Chemical Name:
Limonexic acid
CAS:
99026-99-0
MF:
C26H30O10