Synthesis, structure, and reactivity of secosteroids containing a medium‐sized ring. Part 32. Conformations and photochemical reactivity of some unsaturated 5,10‐secosteroidal ketones
Само за регистроване кориснике
1991
Аутори
Lorenc, Ljubinka B.Pavlović, Vladimir D.
Mihailovíć, Mihailo Lj.
Kalvoda, Jaroslav
Führer, Hermann
Чланак у часопису (Објављена верзија)

Метаподаци
Приказ свих података о документуАпстракт
UV irradiation of the unsaturated (E)‐5,10‐secosteroidal ketones 1 and 6 results, in addition to (E/Z)‐isomerization, in an intramolecular Pateino‐Büchi reaction and, in the case of 1, in transannular cyclization (along with AcOH elimination). The stereochemistry of the observed intramolecular photoprocesses can be explained in terms of ground‐state conformations of the (E)‐seco‐ketones 1 and 6 in solution.
Кључне речи:
UV irradiation / intramolecular photoprocesses / steroids / (E/Z)‐isomerization / Pateino‐Büchi reaction / transannular cyclizationИзвор:
Helvetica Chimica Acta, 1991, 74, 7, 1459-1463Издавач:
- Wiley - VCH Verlag GmbH & Co
DOI: 10.1002/hlca.19910740709
ISSN: 0018-019X; 1522-2675
Scopus: 2-s2.0-84987589527
Институција/група
IHTMTY - JOUR AU - Lorenc, Ljubinka B. AU - Pavlović, Vladimir D. AU - Mihailovíć, Mihailo Lj. AU - Kalvoda, Jaroslav AU - Führer, Hermann PY - 1991 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/4393 AB - UV irradiation of the unsaturated (E)‐5,10‐secosteroidal ketones 1 and 6 results, in addition to (E/Z)‐isomerization, in an intramolecular Pateino‐Büchi reaction and, in the case of 1, in transannular cyclization (along with AcOH elimination). The stereochemistry of the observed intramolecular photoprocesses can be explained in terms of ground‐state conformations of the (E)‐seco‐ketones 1 and 6 in solution. PB - Wiley - VCH Verlag GmbH & Co T2 - Helvetica Chimica Acta T1 - Synthesis, structure, and reactivity of secosteroids containing a medium‐sized ring. Part 32. Conformations and photochemical reactivity of some unsaturated 5,10‐secosteroidal ketones VL - 74 IS - 7 SP - 1459 EP - 1463 DO - 10.1002/hlca.19910740709 ER -
@article{ author = "Lorenc, Ljubinka B. and Pavlović, Vladimir D. and Mihailovíć, Mihailo Lj. and Kalvoda, Jaroslav and Führer, Hermann", year = "1991", abstract = "UV irradiation of the unsaturated (E)‐5,10‐secosteroidal ketones 1 and 6 results, in addition to (E/Z)‐isomerization, in an intramolecular Pateino‐Büchi reaction and, in the case of 1, in transannular cyclization (along with AcOH elimination). The stereochemistry of the observed intramolecular photoprocesses can be explained in terms of ground‐state conformations of the (E)‐seco‐ketones 1 and 6 in solution.", publisher = "Wiley - VCH Verlag GmbH & Co", journal = "Helvetica Chimica Acta", title = "Synthesis, structure, and reactivity of secosteroids containing a medium‐sized ring. Part 32. Conformations and photochemical reactivity of some unsaturated 5,10‐secosteroidal ketones", volume = "74", number = "7", pages = "1459-1463", doi = "10.1002/hlca.19910740709" }
Lorenc, L. B., Pavlović, V. D., Mihailovíć, Mihailo Lj., Kalvoda, J.,& Führer, H.. (1991). Synthesis, structure, and reactivity of secosteroids containing a medium‐sized ring. Part 32. Conformations and photochemical reactivity of some unsaturated 5,10‐secosteroidal ketones. in Helvetica Chimica Acta Wiley - VCH Verlag GmbH & Co., 74(7), 1459-1463. https://doi.org/10.1002/hlca.19910740709
Lorenc LB, Pavlović VD, Mihailovíć, Mihailo Lj., Kalvoda J, Führer H. Synthesis, structure, and reactivity of secosteroids containing a medium‐sized ring. Part 32. Conformations and photochemical reactivity of some unsaturated 5,10‐secosteroidal ketones. in Helvetica Chimica Acta. 1991;74(7):1459-1463. doi:10.1002/hlca.19910740709 .
Lorenc, Ljubinka B., Pavlović, Vladimir D., Mihailovíć, Mihailo Lj., Kalvoda, Jaroslav, Führer, Hermann, "Synthesis, structure, and reactivity of secosteroids containing a medium‐sized ring. Part 32. Conformations and photochemical reactivity of some unsaturated 5,10‐secosteroidal ketones" in Helvetica Chimica Acta, 74, no. 7 (1991):1459-1463, https://doi.org/10.1002/hlca.19910740709 . .