The fresh ''green odor'' of green leaves arises from eight volatile co
mpounds, C-6-aldehydes and C-6-alcohols which include leaf aldehyde, (
2E)-hexenal; and leaf alcohol, (3Z)-hexenol. These volatile compounds
are biosynthesized in green leaves from alpha-linolenic and linoleic a
cids via their respective hydroperoxides. Four enzymes catalyze this b
iosynthetic pathway and among these four, lipoxygenase and hydroperoxi
de lyase (an enzyme system) are particularly interesting. The enzyme s
ystem involved is found bound to the chloroplast membranes of green le
aves. Lipoxygenase adds oxygen stereoselectively to unsaturated fatty
acids having a (1Z,4Z)-pentadiene moiety, for example, alpha-linolenic
and linoleic acids, to produce 13-(S)-hydroperoxides. Hydroperoxide l
yase cleaves the bond between C-12 and C-13 of these hydroperoxides to
form C-6-aldehydes. The activities of the enzymes change throughout t
he growing season and seed development, and appear to be closely relat
ed to the ambient temperature, solar radiation, dark-light conditions,
etc. Synthesis of green odor is described in this review, and in addi
tion, structural relationships between green odor and the sensory prop
erties of n-hexenals and n-hexenols are discussed. The chemistry of th
e formation of ''Lipton black tea aroma'' from leaf alcohol is also ad
dressed. Attention is focused on the biosynthetic pathway by which C-6
-aldehydes are formed from alpha-linolenic and linoleic acids, on the
enzyme system catalyzing the biogeneration of green odor, and on the r
eaction mechanism and the relationships among various stimuli, the env
ironment, and the enzyme activities for producing C-6-aldehydes.