John E. McMurry

Affiliations: 
Cornell University, Ithaca, NY, United States 
Area:
synthetic organic chemistry
Website:
http://chemistry.cornell.edu/faculty/detail.cfm?netid=jem24
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"John McMurry"
Bio:

http://en.wikipedia.org/wiki/John_E._McMurry

Mean distance: 7.35
 
SNBCP

Parents

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Gilbert Stork grad student 1967 Columbia
 (The isoxazole annelation reaction)

Children

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Mitchell Allen Avery grad student 1978 UC Santa Cruz
Thomas Lectka grad student 1991 Cornell
Pierre De Clercq post-doc 1974-1975 UC Santa Cruz
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Publications

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McMurry JE, Siemers NO. (1994) Periplanone total synthesis via intramolecular pinacol coupling Tetrahedron Letters. 35: 4505-4508
McMurry JE, Siemers NO. (1993) On the stereochemistry of the titanium-induced intramolecular pinacol coupling reaction Tetrahedron Letters. 34: 7891-7894
McMurry JE, Lectka T. (1993) Carbocations with bent three-center, two-electron C-H-C bonds Journal of the American Chemical Society. 115: 10167-10173
Mcmurry JE, Lectka T. (1992) Three-center, two-electron C-H-C bonds in organic chemistry Accounts of Chemical Research. 25: 47-53
McMurry JE, Phelan JC. (1991) Synthesis and conformation of unsubstituted calix[4]arene Tetrahedron Letters. 32: 5655-5658
McMurry JE, Dushin RG. (1990) Total synthesis of (±)-isolobophytolide and (±)-crassin by titanium-induced carbonyl coupling Journal of the American Chemical Society. 112: 6942-6949
Falcetta MF, Jordan KD, McMurry JE, et al. (1990) Through-Bond and Through-Space Interactions in a Series of Cyclic Polyenes Journal of the American Chemical Society. 112: 579-586
McMurry JE, Lectka T. (1990) A remarkable alkane protonolysis reaction: Observation of stoichiometric hydrogen formation Journal of the American Chemical Society. 112: 869-870
McMurry JE, Rico JG, Shih Yn. (1989) Synthesis and stereochemistry of sarcophytol B: An anticancer cembranoid Tetrahedron Letters. 30: 1173-1176
McMurry JE, Rico JG. (1989) Synthesis of 1,2-cycloalkanediols by intramolecular titanium-induced pinacol coupling Tetrahedron Letters. 30: 1169-1172
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