Эта публикация цитируется в 2 научных статьях (всего в 2 статьях)
First stereoselective cyclisation in the cembrane series: X-ray structure of (+)-(4R,8R,11S,12E,14S,16R)-11-isopropyl-4,8,14-trimethyl-14-morpholin-4-yl-3-oxa-2-azatricyclo[6.6.2.04,16]hexadeca-1,12-diene
Аннотация:
A simple synthetic derivative of natural diterpene cembrene [(1S,2E,4S,7E,11E)-4-morpholin-4-ylcembra-2,7,11-trien-5-one E-oxime] was found to be highly sensitive to acids (sulfuric and trifluoroacetic), and it is transformed under acidic conditions to atricyclic bridged system with the 5,6-dihydro-4H-1,2-oxazine moiety.
Образец цитирования:
A. M. Agafontsev, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “First stereoselective cyclisation in the cembrane series: X-ray structure of (+)-(4R,8R,11S,12E,14S,16R)-11-isopropyl-4,8,14-trimethyl-14-morpholin-4-yl-3-oxa-2-azatricyclo[6.6.2.04,16]hexadeca-1,12-diene”, Mendeleev Commun., 19:5 (2009), 246–247
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3185
https://www.mathnet.ru/rus/mendc/v19/i5/p246
Эта публикация цитируется в следующих 2 статьяx:
Max M. Majireck, John M. Bennett, Comprehensive Heterocyclic Chemistry IV, 2022, 283
Alexander M. Agafontsev, Tatyana V. Rybalova, Yurii V. Gatilov, Alexey V. Tkachev, “ChemInform Abstract: First Stereoselective Cyclization in the Cembrane Series: X‐Ray Structure of (+)‐(4R,8R,11S,12E,14S,16R) ‐11‐Isopropyl‐4,8,14‐trimethyl‐14‐morpholin‐4‐yl‐3‐oxa‐2‐azatricyclo [6.6.2.04,16]hexadeca‐1,12‐diene.”, ChemInform, 41:7 (2010)
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