Zobrazeno 1 - 10
of 155
pro vyhledávání: '"K. S. Narang"'
Publikováno v:
Proceedings of Indian National Science Academy, Vol 5, Iss 2 (2015)
The Structure of Rottlerin Part III
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::0c3f5507eaeff1e2c10a2a71e02c6271
https://insa.nic.in/writereaddata/UpLoadedFiles/PINSA/Vol05_1939_2_Art09.pdf
https://insa.nic.in/writereaddata/UpLoadedFiles/PINSA/Vol05_1939_2_Art09.pdf
Autor:
M. S. Dhatt, K. S. Narang
Publikováno v:
The Journal of Organic Chemistry. 20:302-305
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a6ffd6853d8acf633b5a6ce02caab9f
https://doi.org/10.1021/jo01121a005
https://doi.org/10.1021/jo01121a005
Autor:
K. S. Narang, G. Sarjit Sandhu, N.K. Ralhan, K. Gandhi, Harkishan Singh, G.M. Sharma, H.S. Sachdev
Publikováno v:
Tetrahedron. 15:53-59
Reactions between α-haloketones and o -carbethoxy phenyl thiourea have been discussed; a mechanism for the observed exclusive formation of 9:10-thiopega-2:10-diene-4-ones in the case of α-haloalkaryl ketones has been advanced and a number of interm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2db26a9597975c2a456d787be0df0bd
https://doi.org/10.1016/0040-4020(61)80007-0
https://doi.org/10.1016/0040-4020(61)80007-0
Publikováno v:
Tetrahedron. 18:1019-1022
Isatin condenses with allyl isothiocyanate in presence of aqueous alcoholic potassium hydroxide at pH 11.81 to give the corresponding 2-mercapto-3-allyl-4-carbalkoxy-4-hydroxy-tetra- hydroquinazoline and the corresponding acid; the dibromo derivative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::440ca1885f7a307e6134e64fb4e31f3c
https://doi.org/10.1016/s0040-4020(01)99265-8
https://doi.org/10.1016/s0040-4020(01)99265-8
Publikováno v:
The Journal of Organic Chemistry. 27:2147-2149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96c6a57ee2ad141f817b72ba4957b12c
https://doi.org/10.1021/jo01053a059
https://doi.org/10.1021/jo01053a059
Publikováno v:
Journal of Medicinal Chemistry. 6:450-452
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::405e8eb83e8c0e64bb66371bff721fad
https://doi.org/10.1021/jm00340a027
https://doi.org/10.1021/jm00340a027
Publikováno v:
J. Chem. Soc. C. :1114-1116
Ethyl 4-allylthioureido-3-aryl-2-imino-4-thiazoline-5-carboxylates (V), obtained by condensation of ethyl 4-amino-3-aryl-2-imino-4-thiazoline-5-carboxylates (I) with allyl isothiocyanate, were converted into 9H-3-aryl-6,7-dihydro-6-methylbisthiazolo[
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::715dc897750e91f2930eade52aef4ccc
https://doi.org/10.1039/j39700001114
https://doi.org/10.1039/j39700001114
Publikováno v:
The Journal of Organic Chemistry. 28:740-742
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56086359b32c8059718689e24ffda931
https://doi.org/10.1021/jo01038a035
https://doi.org/10.1021/jo01038a035
Autor:
AMRIK SINGH, K. S. NARANG
Chemistry Department, Guru Nanak Dev University, Amritsar Manuscript received 11 October 1974; revised 11 August 1975; accepted 12 :August 1975 2-Imino-3-aryl-4-amino-5-carbethoxy-4-thiazolines(III) when condensed with 2-chlorothiazoles (IV) in pheno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c1af7e8c207b329a260176a52e0389a
Autor:
A. Singh, K. S. Narang
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1484df72e929b510a55e278a55f8bdd9
https://doi.org/10.1002/chin.197629212
https://doi.org/10.1002/chin.197629212