Razvoj novih sintetičkih metoda i njihova primena u sintezi prirodnih proizvoda i biološki aktivnih jedinjenja

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Razvoj novih sintetičkih metoda i njihova primena u sintezi prirodnih proizvoda i biološki aktivnih jedinjenja (en)
Развој нових синтетичких метода и њихова примена у синтези природних производа и биолошки активних једињења (sr)
Razvoj novih sintetičkih metoda i njihova primena u sintezi prirodnih proizvoda i biološki aktivnih jedinjenja (sr_RS)
Authors

Publications

Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings

Vulović, Bojan; Bihelović, Filip; Matović, Radomir; Saičić, Radomir N.

(Oxford : Pergamon-Elsevier Science Ltd, 2009)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Saičić, Radomir N.
PY  - 2009
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/1031
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2774
AB  - A combination of organotransition metal catalysis and organocatalysis allows for Tsuji-Trost 5-exo- and 6-exo-cyclizations of aldehydes. This transformation can also be accomplished as a catalytic asymmetric reaction, which affords vinylcyclopentane derivatives with up to 98%ee. (C) 2009 Elsevier Ltd. All rights reserved.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Tetrahedron
T1  - Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings
VL  - 65
IS  - 50
SP  - 10485
EP  - 10494
DO  - 10.1016/j.tet.2009.10.006
ER  - 
@article{
author = "Vulović, Bojan and Bihelović, Filip and Matović, Radomir and Saičić, Radomir N.",
year = "2009",
abstract = "A combination of organotransition metal catalysis and organocatalysis allows for Tsuji-Trost 5-exo- and 6-exo-cyclizations of aldehydes. This transformation can also be accomplished as a catalytic asymmetric reaction, which affords vinylcyclopentane derivatives with up to 98%ee. (C) 2009 Elsevier Ltd. All rights reserved.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Tetrahedron",
title = "Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings",
volume = "65",
number = "50",
pages = "10485-10494",
doi = "10.1016/j.tet.2009.10.006"
}
Vulović, B., Bihelović, F., Matović, R.,& Saičić, R. N.. (2009). Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings. in Tetrahedron
Oxford : Pergamon-Elsevier Science Ltd., 65(50), 10485-10494.
https://doi.org/10.1016/j.tet.2009.10.006
Vulović B, Bihelović F, Matović R, Saičić RN. Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings. in Tetrahedron. 2009;65(50):10485-10494.
doi:10.1016/j.tet.2009.10.006 .
Vulović, Bojan, Bihelović, Filip, Matović, Radomir, Saičić, Radomir N., "Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings" in Tetrahedron, 65, no. 50 (2009):10485-10494,
https://doi.org/10.1016/j.tet.2009.10.006 . .
65
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61

Radical reactions of xanthates: Annulation of the cyclopentene ring

Elheshi, Ahmed Mohamed; Maslak, Veselin; Saičić, Radomir N.

(Belgrade : Serbian Chemical Society, 2007)

TY  - JOUR
AU  - Elheshi, Ahmed Mohamed
AU  - Maslak, Veselin
AU  - Saičić, Radomir N.
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4299
AB  - Homoallylic radicals, generated from the corresponding xanthates, react with terminal alkynes to give cyclopentene derivatives in moderate yields.
AB  - Хомоалилни радикали, настали из одговарајућих ксантата, реагују са терминалним 
алкинима и дају деривате циклопентена у умереним приносима.
PB  - Belgrade : Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Radical reactions of xanthates: Annulation of the cyclopentene ring
T1  - Radikalske reakcije ksantata : anelacija ciklopentenovog prstena
VL  - 72
IS  - 12
SP  - 1173
EP  - 1179
DO  - 10.2298/JSC0712173E
ER  - 
@article{
author = "Elheshi, Ahmed Mohamed and Maslak, Veselin and Saičić, Radomir N.",
year = "2007",
abstract = "Homoallylic radicals, generated from the corresponding xanthates, react with terminal alkynes to give cyclopentene derivatives in moderate yields., Хомоалилни радикали, настали из одговарајућих ксантата, реагују са терминалним 
алкинима и дају деривате циклопентена у умереним приносима.",
publisher = "Belgrade : Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Radical reactions of xanthates: Annulation of the cyclopentene ring, Radikalske reakcije ksantata : anelacija ciklopentenovog prstena",
volume = "72",
number = "12",
pages = "1173-1179",
doi = "10.2298/JSC0712173E"
}
Elheshi, A. M., Maslak, V.,& Saičić, R. N.. (2007). Radical reactions of xanthates: Annulation of the cyclopentene ring. in Journal of the Serbian Chemical Society
Belgrade : Serbian Chemical Society., 72(12), 1173-1179.
https://doi.org/10.2298/JSC0712173E
Elheshi AM, Maslak V, Saičić RN. Radical reactions of xanthates: Annulation of the cyclopentene ring. in Journal of the Serbian Chemical Society. 2007;72(12):1173-1179.
doi:10.2298/JSC0712173E .
Elheshi, Ahmed Mohamed, Maslak, Veselin, Saičić, Radomir N., "Radical reactions of xanthates: Annulation of the cyclopentene ring" in Journal of the Serbian Chemical Society, 72, no. 12 (2007):1173-1179,
https://doi.org/10.2298/JSC0712173E . .
1

Ring closing metathesis/fragmentation route to (Z)-configured medium ring cycloalkenes. Total synthesis of (+/-)-periplanone C

Matović, Radomir; Ivkovic, Aleksandar; Manojlović, Marija; Tokic-Vujosevic, Zorana; Saičić, Radomir N.

(American Chemical Society (ACS), 2006)

TY  - JOUR
AU  - Matović, Radomir
AU  - Ivkovic, Aleksandar
AU  - Manojlović, Marija
AU  - Tokic-Vujosevic, Zorana
AU  - Saičić, Radomir N.
PY  - 2006
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2771
AB  - The combination of ring closing metathesis and beta-fragmentation offers an efficient entry into (Z)-configured medium ring cycloalkenes. The fragmentation step can be effected under anionic or radical conditions. The versatility of this method is demonstrated by the total synthesis of (+/-)-periplanone C - a macrocyclic pheromone of Periplaneta americana.
PB  - American Chemical Society (ACS)
T2  - Journal of Organic Chemistry
T1  - Ring closing metathesis/fragmentation route to (Z)-configured medium ring cycloalkenes. Total synthesis of (+/-)-periplanone C
VL  - 71
IS  - 25
SP  - 9411
EP  - 9419
DO  - 10.1021/jo061790j
ER  - 
@article{
author = "Matović, Radomir and Ivkovic, Aleksandar and Manojlović, Marija and Tokic-Vujosevic, Zorana and Saičić, Radomir N.",
year = "2006",
abstract = "The combination of ring closing metathesis and beta-fragmentation offers an efficient entry into (Z)-configured medium ring cycloalkenes. The fragmentation step can be effected under anionic or radical conditions. The versatility of this method is demonstrated by the total synthesis of (+/-)-periplanone C - a macrocyclic pheromone of Periplaneta americana.",
publisher = "American Chemical Society (ACS)",
journal = "Journal of Organic Chemistry",
title = "Ring closing metathesis/fragmentation route to (Z)-configured medium ring cycloalkenes. Total synthesis of (+/-)-periplanone C",
volume = "71",
number = "25",
pages = "9411-9419",
doi = "10.1021/jo061790j"
}
Matović, R., Ivkovic, A., Manojlović, M., Tokic-Vujosevic, Z.,& Saičić, R. N.. (2006). Ring closing metathesis/fragmentation route to (Z)-configured medium ring cycloalkenes. Total synthesis of (+/-)-periplanone C. in Journal of Organic Chemistry
American Chemical Society (ACS)., 71(25), 9411-9419.
https://doi.org/10.1021/jo061790j
Matović R, Ivkovic A, Manojlović M, Tokic-Vujosevic Z, Saičić RN. Ring closing metathesis/fragmentation route to (Z)-configured medium ring cycloalkenes. Total synthesis of (+/-)-periplanone C. in Journal of Organic Chemistry. 2006;71(25):9411-9419.
doi:10.1021/jo061790j .
Matović, Radomir, Ivkovic, Aleksandar, Manojlović, Marija, Tokic-Vujosevic, Zorana, Saičić, Radomir N., "Ring closing metathesis/fragmentation route to (Z)-configured medium ring cycloalkenes. Total synthesis of (+/-)-periplanone C" in Journal of Organic Chemistry, 71, no. 25 (2006):9411-9419,
https://doi.org/10.1021/jo061790j . .
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