Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Russell L. Underwood"'
Publikováno v:
Tetrahedron: Asymmetry. 7:837-842
A practical synthesis of tetrahydrofuran 7 is reported utilizing the Sharpless epoxidation as the key enantioselective step.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96c19ab66611ebef1dd1dedc1cfbdaa4
https://doi.org/10.1016/0957-4166(96)00081-x
https://doi.org/10.1016/0957-4166(96)00081-x
Publikováno v:
Journal of Medicinal Chemistry. 39:605-608
The R- and S-enantiomers of 2-[[hydroxyl[[2-[(octadecyloxy) methyl]tetrahydrofuran-2-yl]methoxy]-phosphinyl]oxy]-N,N,N,- trimethylethylaminium hydroxide salt (SRI 62-834) have been evaluated in several assays to determine potential antitumor activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df83f9f55e8b257e972695a0ae6bf2cc
https://doi.org/10.1021/jm950072e
https://doi.org/10.1021/jm950072e
Autor:
Kapa Prasad, Chung-Pin Chen, Andrew Kucerovy, Russell L. Underwood, Oljan Repic, Heinrich Estermann
Publikováno v:
The Journal of Organic Chemistry. 60:7693-7696
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daedec575b2fe9365bba1a084503ac1d
https://doi.org/10.1021/jo00128a052
https://doi.org/10.1021/jo00128a052
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72cd0bf69c6c4bb261cfd79fce506016
https://doi.org/10.1002/chin.199245123
https://doi.org/10.1002/chin.199245123
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c0eeff2f3f20a14649d25ba00556d79
https://doi.org/10.1002/chin.199620102
https://doi.org/10.1002/chin.199620102
Publikováno v:
ChemInform. 27
The R- and S-enantiomers of 2-[[hydroxy[[2-[(octadecyloxy)methyl]tetrahydrofuran-2-yl]methoxy]-phosphinyl]oxy]-N,N,N-trimethylethylaminium-hydroxide salt (SRI 62-834) have been evaluated in several assays to determine potential antitumor activity. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95a67893b348b1bfd0943c9afa4ea17a
https://doi.org/10.1002/chin.199619256
https://doi.org/10.1002/chin.199619256
Publikováno v:
The Journal of Organic Chemistry. 57:3250-3252
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::766f95d27c6bafd49b10c114c196934e
https://doi.org/10.1021/jo00037a055
https://doi.org/10.1021/jo00037a055
Autor:
Russell L. Underwood, Bert Fraser-Reid
Publikováno v:
ChemInform. 21
Strategies for the final steps in a synthesis of bactobolin have been examined on substrates obtained by retrograde transformations of actinobilin. It is shown that α-acetamido ketones react with LiCHCl2 from the Re face thereby generating the C-5 c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1b46719aa6036ee0e6452806cec8883
https://doi.org/10.1002/chin.199027329
https://doi.org/10.1002/chin.199027329
Publikováno v:
The Journal of Organic Chemistry. 61:384-385
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33e0a0e5abcba258f7d485bdb379b866
https://doi.org/10.1021/jo9515034
https://doi.org/10.1021/jo9515034
Autor:
Russell L. Underwood, Bert Fraser-Reid
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :731
Strategies for the final steps in a synthesis of bactobolin have been examined on substrates obtained by retrograde transformations of actinobilin. It is shown that α-acetamido ketones react with LiCHCl2 from the Re face thereby generating the C-5 c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e8e5bd2bd83923acee3d90489781112
https://doi.org/10.1039/p19900000731
https://doi.org/10.1039/p19900000731