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T.M. Avignon et al.
Tetrahedron, 47, 7279-7279 (1991)
A Divergent Enantioselective Synthesis of 9-J1-Phytoprostane and 9-A1-Phytoprostane Methyl Ester
Porta A, et al.
European Journal of Organic Chemistry, 2014(10), 2111-2119 (2014)
Journal of the Chemical Society. Chemical Communications, 1371-1371 (1989)
Stereoselective synthesis of 2, 6-trans-tetrahydropyran via primary diamine-catalyzed oxa-conjugate addition reaction of a, ?-unsaturated ketone: Total synthesis of Psymberin
Byeon SR, et al
Organic Letters, 13(21), 5816-5819 (2011)
"Photo-induced chemical vapor generation with formic acid for ultrasensitive atomic fluorescence spectrometric determination of mercury: potential application to mercury speciation in water"
Zheng C, et al.
Journal of Analytical Atomic Spectrometry, 20(08), 746-750 (2005)
S. Takano et al.
Synthesis, 539-539 (1989)
S. Najdi et al.
Tetrahedron Letters, 31, 3279-3279 (1990)
"Determination of four heterocyclic insecticides by ionic liquid dispersive liquid?liquid microextraction in water samples"
Liu Y, et al.
Journal of Chromatography A, 1216(06), 885- 891 (2009)
R.E. Ireland et al.
The Journal of Organic Chemistry, 55, 1423-1423 (1990)
A two-step synthesis of (R)-and (S)-benzylglycidyl ether
Byun HS and Bittman R
Tetrahedron Letters, 30(21), 2751-2754 (1989)
Rocío Marcos et al.
Journal of the American Chemical Society, 130(50), 16838-16839 (2008-12-05)
Enantiomerically pure aryl and benzyl glycidyl ethers undergo stereospecific cyclizations leading to 3-chromanols or to tetrahydrobenzo[c]oxepin-4-ols under mild conditions in the presence of a catalytic amount of FeBr3/3AgOTf. The same processes are also mediated, albeit in a much less efficient
S. Takano et al.
Tetrahedron Letters, 31, 3619-3619 (1990)
M. Honda et al.
Chemical & Pharmaceutical Bulletin, 39, 1385-1385 (1991)
B.H. Lipshutz et al.
Organic Syntheses, 69, 80-80 (1990)
Michael T Crimmins et al.
Journal of the American Chemical Society, 126(40), 12790-12791 (2004-10-08)
The enantioselective synthesis of the potent, selective, cytotoxic, annonaceous acetogenin, (+)-gigantecin, has been completed. An asymmetric glycolate aldol serves to establish the stereocenters at C13,14 and at C21,22. A Carreira asymmetric acetylide addition is used to establish the C17 stereocenter.
Neeraj Bala et al.
Journal of basic microbiology, 52(4), 383-389 (2011-11-05)
The incubation of whole Bacillus alcalophilus cells grown on a mineral supplemented medium (MSM) containing 1% (w/v) sucrose as carbon source, 1.2% (w/v) tryptone as nitrogen source at pH 6.5 and temperature 30 °C in 24 h kinetically resolved benzyl
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