Biosynthesis and enantioselectivity in the production of the lilac compounds in Actinidia arguta flowers.

[1]  Yizeng Liang,et al.  Determination of Essential Oil Composition from Osmanthus fragrans Tea by GC-MS Combined with a Chemometric Resolution Method , 2010, Molecules.

[2]  N. Dudareva,et al.  Two terpene synthases are responsible for the major sesquiterpenes emitted from the flowers of kiwifruit (Actinidia deliciosa) , 2009, Journal of experimental botany.

[3]  E. Pichersky,et al.  Overexpression of the lemon basil alpha-zingiberene synthase gene increases both mono- and sesquiterpene contents in tomato fruit. , 2008, The Plant journal : for cell and molecular biology.

[4]  E. F. Walton,et al.  Analysis of expressed sequence tags from Actinidia: applications of a cross species EST database for gene discovery in the areas of flavor, health, color and ripening , 2008, BMC Genomics.

[5]  D. Comeskey,et al.  Chirality and biosynthesis of lilac compounds in Actinidia arguta flowers. , 2007, Phytochemistry.

[6]  A. Matich,et al.  Lilac alcohol epoxide: a linalool derivative in Actinidia arguta flowers. , 2006, Phytochemistry.

[7]  M. Reichelt,et al.  The nonmevalonate pathway supports both monoterpene and sesquiterpene formation in snapdragon flowers. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[8]  H. Bouwmeester,et al.  Enantiospecific (+)- and (-)-germacrene D synthases, cloned from goldenrod, reveal a functionally active variant of the universal isoprenoid-biosynthesis aspartate-rich motif. , 2004, Archives of biochemistry and biophysics.

[9]  A. Aharoni,et al.  Gain and Loss of Fruit Flavor Compounds Produced by Wild and Cultivated Strawberry Species , 2004, The Plant Cell Online.

[10]  N. Kubota,et al.  Enantioselective glucosylation of (±)-secondary alcohols with plant glucosyltransferases , 2004 .

[11]  A. Mosandl,et al.  Biogenetic studies in Syringa vulgaris L.: bioconversion of (18)O(2H)-labeled precursors into lilac aldehydes and lilac alcohols. , 2003, Journal of agricultural and food chemistry.

[12]  H. Young,et al.  Actinidia arguta: volatile compounds in fruit and flowers. , 2003, Phytochemistry.

[13]  A. Mosandl,et al.  Biogenetic studies in Syringa vulgaris L.: synthesis and bioconversion of deuterium-labeled precursors into lilac aldehydes and lilac alcohols. , 2003, Journal of agricultural and food chemistry.

[14]  D. Korchagina,et al.  Rearrangements of Epoxides of Linalool and Nerolidyl Acetate in Acid Media , 2002 .

[15]  L. Mondello,et al.  Multidimensional capillary GC-GC for the analysis of complex samples. 5. Enantiomeric distribution of monoterpene hydrocarbons, monoterpene alcohols, and linalyl acetate of bergamot (Citrus bergamia Risso et Poiteau) oils , 1998 .

[16]  R. Croteau,et al.  Monoterpene Synthases from Common Sage (Salvia officinalis)* , 1998, The Journal of Biological Chemistry.

[17]  F. Fleig,et al.  Enantiomeric Distribution Studies of Linalool and Linalyl Acetate. A Powerful Tool for Authenticity Control of Essential Oils , 1998 .

[18]  D. Knorr,et al.  Conversion of menthyl acetate or neomenthyl acetate into menthol or neomenthol by cell suspension cultures of Mentha canadensis and Mentha piperita , 1993 .

[19]  K. Sharpless,et al.  High stereo- and regioselectivities in the transition metal catalyzed epoxidations of olefinic alcohols by tert-butyl hydroperoxide , 1973 .

[20]  M. Ohno,et al.  The Synthesis and Absolute Configurations of Lilac Alcohols , 1971 .

[21]  OhnoMasaji,et al.  Lilac Alcohol-a and -b, New Naturally Occurring Odorous Ingredients , 1970 .

[22]  A. Matich,et al.  The enantiomeric composition of linalool and linalool oxide in the flowers of kiwifruit (Actinidia) species. , 2010, Chirality.

[23]  A. Matich,et al.  Deceit and Deception in Volatile Analysis , 2008 .

[24]  H. Bouwmeester,et al.  Mechanisms of the biosynthesis of sesquiterpene enantiomers (+)‐ and (−)‐germacrene D in Solidago canadensis , 1999 .

[25]  M. Ohno,et al.  odorous constituents of lilac flower oil , 1971 .

[26]  D. D. Perrin,et al.  Purification of Laboratory Chemicals , 2022 .