Zobrazeno 1 - 10
of 365
pro vyhledávání: '"William G. Dauben"'
Publikováno v:
Bioorganic & Medicinal Chemistry. 7:2937-2944
Endothal (1diacid) and [3H]cantharidic acid ([3H]CA) bind with high affinity to the catalytic subunit of protein phosphatase 2A (PP2A). PP2A in liver cytosol was greatly stabilized with 30% glycerol as a preliminary step in the potential use of endot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6482f3e4cdc4bc40e5a28e463aca1fad
https://doi.org/10.1016/s0968-0896(99)00239-4
https://doi.org/10.1016/s0968-0896(99)00239-4
Publikováno v:
Tetrahedron Letters. 39:7079-7082
The synthesis of the basic tricyclic nucleus of the trinervitane diterpenes by means of the Robinson annelation and McMurry coupling is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05b5049adaaaed5a54dc9cf42d41d086
https://doi.org/10.1016/s0040-4039(98)01469-5
https://doi.org/10.1016/s0040-4039(98)01469-5
Publikováno v:
The Journal of Organic Chemistry. 63:1379-1389
The Pauson−Khand reaction of cyclobutenes 3−5 with a variety of acetylenes yielded cis-anti cis-tricyclo[5.3.0.02,6]decanes 9−17. The unwanted regioisomers 9a and 10a were the sole products using acetylene, but there was a remarkable reversal i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21bebd73761f111f0f0b81f83a8c58ad
https://doi.org/10.1021/jo9708194
https://doi.org/10.1021/jo9708194
Publikováno v:
The Journal of Organic Chemistry. 62:9005-9008
Two structural previtamin D3 analogues (R = H, CH3) cyclized photochemically with a 1.4−1.8-fold increase in quantum yields over a 3-nm change in excitation wavelength. The sudden increase in quantum yields is due to the participation and mixing of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88549fd5ce349b8181bf825ab1f0be7a
https://doi.org/10.1021/jo9622183
https://doi.org/10.1021/jo9622183
Autor:
Xiaoming Zhang, William G. Dauben, Michael J. Luzzio, Shung C. Wu, Bipin Pandy, Robert T. Hendricks
Publikováno v:
Tetrahedron Letters. 36:2385-2388
Two efficient enantioselective syntheses of an A-ring precursor to 1 α,25-dihydroxyvitamin D3 have been developed. The key step in these sequences involves the stereoselective cyclopropanation of a chiral γ-alkoxy-α-diazo-β-keto ester. In one seq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ec2a33f13ab49da1c0977250d82668e
https://doi.org/10.1016/0040-4039(95)00284-j
https://doi.org/10.1016/0040-4039(95)00284-j
Publikováno v:
Tetrahedron Letters. 35:2149-2152
Beginning with a steroid-5-ene, C/D-ring synthons of vitamin D are readily prepared via ozonization followed by a Norrish II photoelimination reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::917bb7ed1952e50f89799ab1a2d52828
https://doi.org/10.1016/s0040-4039(00)76782-7
https://doi.org/10.1016/s0040-4039(00)76782-7
Publikováno v:
ChemInform. 22
Montmorillonite clays catalyze the rearrangement of substituted allyl phenyl ethers to provide ortho -allyl phenols, chromans and coumarans under mild conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96b48390ea9205ff434e0fc1c4ddc402
https://doi.org/10.1002/chin.199128067
https://doi.org/10.1002/chin.199128067
Autor:
P. Koehler, William G. Dauben
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::066464401dc65093d76f82fc9152dc18
https://doi.org/10.1002/chin.199103325
https://doi.org/10.1002/chin.199103325
Autor:
A. S. Funhoff, R. R. Jun. Ollmann, S. S. Leung, J. E. Bishop, William G. Dauben, A. W. Norman
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f704a787c0cffb372c77335d47a73aa0
https://doi.org/10.1002/chin.199221224
https://doi.org/10.1002/chin.199221224
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f73a1d4db0888111712cfa25fcbd31e
https://doi.org/10.1002/chin.199143207
https://doi.org/10.1002/chin.199143207