Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Gayane Godjoian"'
Publikováno v:
Tetrahedron. 54:8919-8932
Reduction of malonaldehyde bis(ethylene and propylene acetals) with borane or monochloroborane produces diether diols 1 and 2 in high yield. Similar reduction of glyoxal bis(ethylene acetals) has only limited utility for the preparation of tetrasubst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7aaeb991e9d336021998a7228e4da247
https://doi.org/10.1016/s0040-4020(98)00563-8
https://doi.org/10.1016/s0040-4020(98)00563-8
Autor:
Gayane Godjoian, Bakthan Singaram
Publikováno v:
Tetrahedron Letters. 38:1717-1720
Several tertiary amides were reduced using one or two equivalents of various dialkylboranes, such as 9-borabicyclo[3.3.1] nonane (9-BBN), dicyclohexylborane (Chx2BH), or disiamylborane (Sia2BH). The reduction of tertiary amides having alkyl substitue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b738d547c91e01c8358cc413ed03779d
https://doi.org/10.1016/s0040-4039(97)00179-2
https://doi.org/10.1016/s0040-4039(97)00179-2
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 119:93-112
Acyclic tetradentate organosulfur ligands of the type S2X2 (where X = S.O.N) can be efficiently prepared by selective desulfurization of bis(1,3-dithiolanes) and bis(1,3-dithianes); bis(1,3-oxathiolanes); and bis(thiazolidines) with two equivalents o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3785f30fdac6a107e7b9166a3608b40
https://doi.org/10.1080/10426509608043468
https://doi.org/10.1080/10426509608043468
Autor:
Gayane Godjoian, Vivian R Wang, Alfredo M Ayala, Carlos G. Gutierrez, Ruben V Martínez, Rolando Martínez-Bernhardt
Publikováno v:
Tetrahedron Letters. 37:433-436
Stannylene acetals prepared from disubstituted vicinal diols can be alkylated with a half equivalent of 1,2-dibromoethane to produce tetrasubstituted triethylene glycols 2 , or with two equivalents of 2-chloroethanol to produce disubstituted triethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5905e8298bc8763c87421ae7045a1127
https://doi.org/10.1016/0040-4039(95)02211-2
https://doi.org/10.1016/0040-4039(95)02211-2
Autor:
Eric R. Marinez, Ging S. Lee, Asmik Oganesyan, Ghiwa Sabih, Jude N. Bashara, Gayane Godjoian, Hieu M. Duong, Carlos G. Gutierrez
Publikováno v:
Organic Letters. 6:1705-1707
New adamantane derivatives 1 and 2 that bear functionalized one-carbon extensions at all four bridgehead positions have been prepared. Radical nucleophilic substitution (S(RN)1) reaction of 1,3,5,7-tetrabromoadamantane with cyanide produces 1,3,5,7-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35d81c582c692f4363ea041f8ec8f6bd
https://doi.org/10.1021/ol036526g
https://doi.org/10.1021/ol036526g
Autor:
Vivian R Wang, Gayane Godjoian, Rolando Martínez-Bernhardt, Alfredo M Ayala, Carlos G. Gutierrez, Ruben V Martínez
Publikováno v:
ChemInform. 27
Stannylene acetals prepared from disubstituted vicinal diols can be alkylated with a half equivalent of 1,2-dibromoethane to produce tetrasubstituted triethylene glycols 2 , or with two equivalents of 2-chloroethanol to produce disubstituted triethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44e1c5c5031f66b2627189c51b2e2abf
https://doi.org/10.1002/chin.199619084
https://doi.org/10.1002/chin.199619084
Autor:
Gayane Godjoian, Bakthan Singaram
Publikováno v:
ChemInform. 28
Several tertiary amides were reduced using one or two equivalents of various dialkylboranes, such as 9-borabicyclo[3.3.1] nonane (9-BBN), dicyclohexylborane (Chx2BH), or disiamylborane (Sia2BH). The reduction of tertiary amides having alkyl substitue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1248ac9adb0e46728db891655b2d6a4f
https://doi.org/10.1002/chin.199726073
https://doi.org/10.1002/chin.199726073
ChemInform Abstract: Substituted Diether Diols by Ring-Opening of Carbocyclic and Stannylene Acetals
Publikováno v:
ChemInform. 29
Reduction of malonaldehyde bis(ethylene and propylene acetals) with borane or monochloroborane produces diether diols 1 and 2 in high yield. Similar reduction of glyoxal bis(ethylene acetals) has only limited utility for the preparation of tetrasubst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f16a4ef796b4df5ba0623cd6b2eb32ca
https://doi.org/10.1002/chin.199846086
https://doi.org/10.1002/chin.199846086
Publikováno v:
ACS Symposium Series ISBN: 9780841233812
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::102bd3a5a191895a10d1a41b3a8dd534
https://doi.org/10.1021/bk-1996-0641.ch010
https://doi.org/10.1021/bk-1996-0641.ch010
Publikováno v:
The Journal of Organic Chemistry. 59:7193-7194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77dc1afd8aeef840f0d0dc999ae11374
https://doi.org/10.1021/jo00103a004
https://doi.org/10.1021/jo00103a004