Zobrazeno 1 - 6
of 6
pro vyhledávání: '"F. Jan Dommerholt"'
Autor:
J. G. H. Willems, Jeannet B. Hammink, F. Jan Dommerholt, Lambertus Thijs, Binne Zwanenburg, Ariëla M. Vaarhorst
Publikováno v:
Tetrahedron Letters. 36:603-606
Asymmetric borane reduction of acetophenone using 1,3,2-oxazaborolidines derived from aziridine-2-tertiairy alcohols 1 and 2 yielded the corresponding alcohol in high optical yields. The synthesis of the novel chiral catalysts 1 and 2 using D-and L-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52d846d336fad091e6fac588dd909804
https://doi.org/10.1016/0040-4039(94)02313-z
https://doi.org/10.1016/0040-4039(94)02313-z
Publikováno v:
Journal of Agricultural and Food Chemistry. 40:1230-1235
A high yield preparation procedure for the germination stimulant GR24 (2) is described. Improvements were introduced in the syntheses of the key building blocks 3 and 4. The tricyclic lactone 3 was prepared from indan-1-one in four steps. The major i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f2c6dbcf59f823c1efb5fb122e60588
https://doi.org/10.1021/jf00019a031
https://doi.org/10.1021/jf00019a031
Autor:
Quirinus B. Broxterman, Peter N. M. Botman, René de Gelder, Hans E. Schoemaker, Richard H. Blaauw, F. Jan Dommerholt, Floris P. J. T. Rutjes
Publikováno v:
ChemInform. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0197a09695e53f7002ec03384f83fc75
https://doi.org/10.1002/chin.200519209
https://doi.org/10.1002/chin.200519209
Autor:
F. Jan Dommerholt, Hans E. Schoemaker, and Floris P. J. T. Rutjes, René de Gelder, Richard H. Blaauw, Quirinus B. Broxterman, Peter N. M. Botman
Publikováno v:
Organic Letters, 6, 1523-7060
Organic Letters, 6, 26, pp. 1523-7060
Organic Letters, 6, 4941-4
Organic Letters, 6, 4941-4944. American Chemical Society
Organic Letters, 6, 26, pp. 4941-4
Organic Letters, 6, 26, pp. 1523-7060
Organic Letters, 6, 4941-4
Organic Letters, 6, 4941-4944. American Chemical Society
Organic Letters, 6, 26, pp. 4941-4
Contains fulltext : 57199.pdf (Publisher’s version ) (Closed access) [reaction: see text] Herein, we report a diastereoselective synthesis of the natural product (2S,5R)-5-hydroxypipecolic acid and 6-substituted derivatives thereof. The key step in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1a1fa98c837d33db8c3e04ec174de9a
http://hdl.handle.net/2066/58611
http://hdl.handle.net/2066/58611
Autor:
M. C. Hersmis, J. G. H. Willems, Lambertus Thijs, J. B. Hammink, R. de Gelder, F. Jan Dommerholt, Binne Zwanenburg, Jan M. M. Smits
Publikováno v:
Journal of the Chemical Society-Perkin Transactions 1, 6, pp. 963-967
Journal of the Chemical Society-Perkin Transactions 1, 963-967. Royal soc chemistry
STARTPAGE=963;ENDPAGE=967;ISSN=0300-922X;TITLE=Journal of the Chemical Society-Perkin Transactions 1
Journal of the Chemical Society-Perkin Transactions 1, 963-967. Royal soc chemistry
STARTPAGE=963;ENDPAGE=967;ISSN=0300-922X;TITLE=Journal of the Chemical Society-Perkin Transactions 1
A convenient multigram ‘one pot procedure’ for the synthesis of methyl N-tritylaziridine-2-carboxylates 1 and 2, starting from the N-tritylmethyl esters of L-serine 9 and L-threonine 10 and using methanesulfonyl chloride and triethylamine, is des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d00c5002e24cf7169c2d7478afdf7d
https://hdl.handle.net/2066/28869
https://hdl.handle.net/2066/28869
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