TY  - JOUR
AU  - Grigg, Ronald
AU  - Husinec, Suren
AU  - Savić, Vladimir
PY  - 2010
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1417
AB  - Stereoselective cyclo-addition reactions of azomethine ylides promoted by in situ generated Ag(I)/bisphosphine complexes were studied. Under the optimized conditions, the pyrrolidine products were isolated in up to 84 % yield and with up to 71% e.e. The effects of various reaction variables on the stereoselectivity were also investigated.
AB  - Proučavane su stereoselektivne cikloadicione reakcije azometinskih ilida katalizovane kompleksima srebra i bisfosfinskog liganda generisanih in situ. Pirolidinski derivati izolovani su u dobrim prinosima i sa enantioselektivnošću do 71%. Proučavani su takođe i efekti reakcionih uslova na stereoselektivnost ovih reakcija.
PB  - Srpsko hemijsko društvo, Beograd
T2  - Journal of the Serbian Chemical Society
T1  - Stereoselective cyclo-addition reactions of azomethine ylides catalysed by in situ generated Ag(I)/bisphosphine complexes
T1  - Stereoselektivne cikloadicione reakcije azometinskih ilida katalizovane in situ generisanim Ag(I)/bisfosfinskim kompleksima
VL  - 75
IS  - 1
SP  - 1
EP  - 9
DO  - 10.2298/JSC1001001G
ER  - 

@article{
author = "Grigg, Ronald and Husinec, Suren and Savić, Vladimir",
year = "2010",
abstract = "Stereoselective cyclo-addition reactions of azomethine ylides promoted by in situ generated Ag(I)/bisphosphine complexes were studied. Under the optimized conditions, the pyrrolidine products were isolated in up to 84 % yield and with up to 71% e.e. The effects of various reaction variables on the stereoselectivity were also investigated., Proučavane su stereoselektivne cikloadicione reakcije azometinskih ilida katalizovane kompleksima srebra i bisfosfinskog liganda generisanih in situ. Pirolidinski derivati izolovani su u dobrim prinosima i sa enantioselektivnošću do 71%. Proučavani su takođe i efekti reakcionih uslova na stereoselektivnost ovih reakcija.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "Journal of the Serbian Chemical Society",
title = "Stereoselective cyclo-addition reactions of azomethine ylides catalysed by in situ generated Ag(I)/bisphosphine complexes, Stereoselektivne cikloadicione reakcije azometinskih ilida katalizovane in situ generisanim Ag(I)/bisfosfinskim kompleksima",
volume = "75",
number = "1",
pages = "1-9",
doi = "10.2298/JSC1001001G"
}

Grigg, R., Husinec, S.,& Savić, V.. (2010). Stereoselective cyclo-addition reactions of azomethine ylides catalysed by in situ generated Ag(I)/bisphosphine complexes. in Journal of the Serbian Chemical Society
Srpsko hemijsko društvo, Beograd., 75(1), 1-9.
https://doi.org/10.2298/JSC1001001G

Grigg R, Husinec S, Savić V. Stereoselective cyclo-addition reactions of azomethine ylides catalysed by in situ generated Ag(I)/bisphosphine complexes. in Journal of the Serbian Chemical Society. 2010;75(1):1-9.
doi:10.2298/JSC1001001G .

Grigg, Ronald, Husinec, Suren, Savić, Vladimir, "Stereoselective cyclo-addition reactions of azomethine ylides catalysed by in situ generated Ag(I)/bisphosphine complexes" in Journal of the Serbian Chemical Society, 75, no. 1 (2010):1-9,
https://doi.org/10.2298/JSC1001001G . .

TY  - JOUR
AU  - Cleghorn, Laura A. T.
AU  - Grigg, Ronald
AU  - Savić, Vladimir
AU  - Simić, Milena
PY  - 2008
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1122
AB  - Allylation of alpha,beta-unsaturated aldehydes and cyclic ketones promoted by Pd/In transmetallation processes has been Studied. The unsaturated aldehydes underwent regioselective 1,2-addition to afford secondary homoally alcohols. The reactions have been performed using Pd(OAc)(2)/PPh(3) as catalytic system and metallic indium affording the products in good yields. The same transformation with unsaturated ketones proved to be less efficient, while saturated cyclic ketones delivered generally excellent yields in the presence of Cul. In these latter processes the presence of a distal heteroatom influences the reaction rate.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - Reactive organoallyl species generated from aryl halides and allene: allylation of alpha,beta-unsaturated aldehydes and cyclic ketones employing Pd/In transmetallation processes
VL  - 64
IS  - 37
SP  - 8731
EP  - 8737
DO  - 10.1016/j.tet.2008.06.100
ER  - 

@article{
author = "Cleghorn, Laura A. T. and Grigg, Ronald and Savić, Vladimir and Simić, Milena",
year = "2008",
abstract = "Allylation of alpha,beta-unsaturated aldehydes and cyclic ketones promoted by Pd/In transmetallation processes has been Studied. The unsaturated aldehydes underwent regioselective 1,2-addition to afford secondary homoally alcohols. The reactions have been performed using Pd(OAc)(2)/PPh(3) as catalytic system and metallic indium affording the products in good yields. The same transformation with unsaturated ketones proved to be less efficient, while saturated cyclic ketones delivered generally excellent yields in the presence of Cul. In these latter processes the presence of a distal heteroatom influences the reaction rate.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "Reactive organoallyl species generated from aryl halides and allene: allylation of alpha,beta-unsaturated aldehydes and cyclic ketones employing Pd/In transmetallation processes",
volume = "64",
number = "37",
pages = "8731-8737",
doi = "10.1016/j.tet.2008.06.100"
}

Cleghorn, L. A. T., Grigg, R., Savić, V.,& Simić, M.. (2008). Reactive organoallyl species generated from aryl halides and allene: allylation of alpha,beta-unsaturated aldehydes and cyclic ketones employing Pd/In transmetallation processes. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford., 64(37), 8731-8737.
https://doi.org/10.1016/j.tet.2008.06.100

Cleghorn LAT, Grigg R, Savić V, Simić M. Reactive organoallyl species generated from aryl halides and allene: allylation of alpha,beta-unsaturated aldehydes and cyclic ketones employing Pd/In transmetallation processes. in Tetrahedron Letters. 2008;64(37):8731-8737.
doi:10.1016/j.tet.2008.06.100 .

Cleghorn, Laura A. T., Grigg, Ronald, Savić, Vladimir, Simić, Milena, "Reactive organoallyl species generated from aryl halides and allene: allylation of alpha,beta-unsaturated aldehydes and cyclic ketones employing Pd/In transmetallation processes" in Tetrahedron Letters, 64, no. 37 (2008):8731-8737,
https://doi.org/10.1016/j.tet.2008.06.100 . .

TY  - JOUR
AU  - Grigg, Ronald
AU  - Blacker, John
AU  - Kilner, Colin
AU  - McCaffrey, Shaun
AU  - Savić, Vladimir
AU  - Sridharan, Visuvanathar
PY  - 2008
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1115
AB  - A new, highly efficient synthesis of chiral beta(2.3)-disubstituted-beta-amino acid derivatives has been developed, based on an allylation procedure employing allene and a catalytic Pd/In bimetallic process.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - Stereoselective synthesis of chiral beta(2,3)-disubstituted-beta-amino acid derivatives using Pd/In transmetallation cascade processes
VL  - 64
IS  - 35
SP  - 8177
EP  - 8181
DO  - 10.1016/j.tet.2008.06.037
ER  - 

@article{
author = "Grigg, Ronald and Blacker, John and Kilner, Colin and McCaffrey, Shaun and Savić, Vladimir and Sridharan, Visuvanathar",
year = "2008",
abstract = "A new, highly efficient synthesis of chiral beta(2.3)-disubstituted-beta-amino acid derivatives has been developed, based on an allylation procedure employing allene and a catalytic Pd/In bimetallic process.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "Stereoselective synthesis of chiral beta(2,3)-disubstituted-beta-amino acid derivatives using Pd/In transmetallation cascade processes",
volume = "64",
number = "35",
pages = "8177-8181",
doi = "10.1016/j.tet.2008.06.037"
}

Grigg, R., Blacker, J., Kilner, C., McCaffrey, S., Savić, V.,& Sridharan, V.. (2008). Stereoselective synthesis of chiral beta(2,3)-disubstituted-beta-amino acid derivatives using Pd/In transmetallation cascade processes. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford., 64(35), 8177-8181.
https://doi.org/10.1016/j.tet.2008.06.037

Grigg R, Blacker J, Kilner C, McCaffrey S, Savić V, Sridharan V. Stereoselective synthesis of chiral beta(2,3)-disubstituted-beta-amino acid derivatives using Pd/In transmetallation cascade processes. in Tetrahedron Letters. 2008;64(35):8177-8181.
doi:10.1016/j.tet.2008.06.037 .

Grigg, Ronald, Blacker, John, Kilner, Colin, McCaffrey, Shaun, Savić, Vladimir, Sridharan, Visuvanathar, "Stereoselective synthesis of chiral beta(2,3)-disubstituted-beta-amino acid derivatives using Pd/In transmetallation cascade processes" in Tetrahedron Letters, 64, no. 35 (2008):8177-8181,
https://doi.org/10.1016/j.tet.2008.06.037 . .