ID Name Structure References (top 5) Molecular Target(s)
1ID:8311
L-PINENE

Freqency:
in 1 ingredients:

  • 733
  • in 9 recipes:

  • 37
  • 83
  • 268
  • 339
  • 342
  • 345
  • 352
  • 359
  • 438

  • Properties
    C10H16    136.23





    1:  Darensbourg DJ, Wildeson JR, Lewis SJ, Yarbrough JC.
    Solution and solid-state structural studies of epoxide adducts of cadmium phenoxides. Chemistry relevant to epoxide activation for ring-opening reactions.
    J Am Chem Soc.    impact factor:   5.537
    2002;  124(24): 7075-83

    2:  Martin D, Tholl D, Gershenzon J, Bohlmann J.
    Methyl jasmonate induces traumatic resin ducts, terpenoid resin biosynthesis, and terpenoid accumulation in developing xylem of Norway spruce stems.
    Plant Physiol.    impact factor:   4.434
    2002;  129(3): 1003-18

    3:  Loreto F, Ciccioli P, Cecinato A, Brancaleoni E, Frattoni M, Tricoli D.
    Influence of Environmental Factors and Air Composition on the Emission of [alpha]-Pinene from Quercus ilex Leaves.
    Plant Physiol.    impact factor:   4.434
    1996;  110(1): 267-275

    4:  Loreto F, Ciccioli P, Cecinato A, Brancaleoni E, Frattoni M, Fabozzi C, Tricoli D.
    Evidence of the Photosynthetic Origin of Monoterpenes Emitted by Quercus ilex L. Leaves by 13C Labeling.
    Plant Physiol.    impact factor:   4.434
    1996;  110(4): 1317-1322

    5:  Rogic MM.
    How borane reagents based on alpha-pinene control stereoselectivity in the reductions of carbonyl groups with different stereogenic elements. 3. The effect of the relative size and conformation of the carbonyl substituents on the stereoselectivity of the Ipc(2)BCl, Eap(2)BCl, B-t-Bu-IpcBCl, and B-t-Bu-EapBCl reagents. A semiempirical study
    J Org Chem.    impact factor:   3.44
    2000;  65(21): 6868-75

     
    Time used: 93 milliseconds.

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