13423

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Showing 1-16 of 16 results for "13423" within Papers

T.M. Avignon et al.

Tetrahedron, 47, 7279-7279 (1991)

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)

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)

S. Najdi et al.

Tetrahedron Letters, 31, 3279-3279 (1990)

Journal of the Chemical Society. Chemical Communications, 1371-1371 (1989)

"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)

A two-step synthesis of (R)-and (S)-benzylglycidyl ether

Byun HS and Bittman R

Tetrahedron Letters, 30(21), 2751-2754 (1989)

Metal-mediated cyclization of aryl and benzyl glycidyl ethers: a complete scenario.

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

Bioresolution of benzyl glycidyl ether using whole cells of Bacillus alcalophilus.

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

Enantioselective total synthesis of (+)-gigantecin: exploiting the asymmetric glycolate aldol reaction.

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.

S. Takano et al.

Tetrahedron Letters, 31, 3619-3619 (1990)

R.E. Ireland et al.

The Journal of Organic Chemistry, 55, 1423-1423 (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)

B.H. Lipshutz et al.

Organic Syntheses, 69, 80-80 (1990)

M. Honda et al.

Chemical & Pharmaceutical Bulletin, 39, 1385-1385 (1991)

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