Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Theodore Axenrod"'
Autor:
Farhad Forohar, Mira Kaselj, Richard Gilardi, Nirupam J. Trivedi, Theodore Axenrod, Kajal K. Das, P. R. Dave, Jianguang Sun, Judith L. Flippen-Anderson
Publikováno v:
The Journal of Organic Chemistry. 65:1200-1206
Three synthetic routes to 5-substituted 1,3-diazacyclohexane derivatives 1 are reported. The first method involves treatment of 1, 3-diaminopropan-2-ol 2 with paraformaldehyde to yield 5-hydroxy-1, 3-diazacyclohexane 3. A second method is based on th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4012aede26f5b6a6f5091d9b09a9608
https://doi.org/10.1021/jo991524o
https://doi.org/10.1021/jo991524o
Publikováno v:
Organic Preparations and Procedures International. 29:358-361
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4cf9944fc94dface4ac4c22dc6a110f
https://doi.org/10.1080/00304949709355213
https://doi.org/10.1080/00304949709355213
Publikováno v:
The Journal of Organic Chemistry. 60:6946-6952
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::748afe1b8290f2b75433bc1be8797db9
https://doi.org/10.1021/jo00126a054
https://doi.org/10.1021/jo00126a054
Publikováno v:
Tetrahedron Letters. 34:6677-6680
The t-butyldimethylsilyl ether of 3-(p-toluenesulfonamido)propane-2-ol-1-(p-toluenesulfonate) on treatment with LiH undergoes ring closure to the correponding azetidine which is readily converted to N-tosyl-3-azetidinone oxime. By oxidative nitrolysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e8658c35bd5975e08a927806699abb5
https://doi.org/10.1016/s0040-4039(00)61673-8
https://doi.org/10.1016/s0040-4039(00)61673-8
Publikováno v:
ChemInform. 25
The t-butyldimethylsilyl ether of 3-(p-toluenesulfonamido)propane-2-ol-1-(p-toluenesulfonate) on treatment with LiH undergoes ring closure to the correponding azetidine which is readily converted to N-tosyl-3-azetidinone oxime. By oxidative nitrolysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9be2af7a080323340b72668513d5e443
https://doi.org/10.1002/chin.199401182
https://doi.org/10.1002/chin.199401182
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15cf77a51f1b7f9b818687097e9f39b5
https://doi.org/10.1002/chin.199735066
https://doi.org/10.1002/chin.199735066
Autor:
Theodore Axenrod, F. Forohar, Kajal K. Das, L. Qi, H. Yazdekhasti, C. Watnick, Paritosh R. Dave
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51c908385e19c5ff8f44fd9c7342d696
https://doi.org/10.1002/chin.199735134
https://doi.org/10.1002/chin.199735134
Autor:
Richard Gilardi, Farhad Forohar, Nirupam J. Trivedi, Mira Kaselj, P. R. Dave, Jianguang Sun, Judith L. Flippen-Anderson, Theodore Axenrod, Kajal K. Das
Publikováno v:
ChemInform. 31
Three synthetic routes to 5-substituted 1,3-diazacyclohexane derivatives 1 are reported. The first method involves treatment of 1,3-diaminopropan-2-ol 2 with paraformaldehyde to yield 5-hydroxy-1,3-diazacyclohexane 3. A second method is based on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b379a4e649fe4f6c516e7de773dc2f09
https://doi.org/10.1002/chin.200023157
https://doi.org/10.1002/chin.200023157
Autor:
Paritosh R. Dave, Rongji Dai, Jianguang Sun, Nirupam J. Trivedi, Richard Gilardi, Kaipenchery A. Kumar, Xiao-Pei Guan, Theodore Axenrod, Kajal K. Das, Rajagopal Duddu
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0071dbdf4a2d389e13133b9fc6c52b5b
https://doi.org/10.1002/chin.200024071
https://doi.org/10.1002/chin.200024071
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8088ebb7a3b6ec44f18e2a1632dcf89b
https://doi.org/10.1002/chin.200135173
https://doi.org/10.1002/chin.200135173