| Year |
Citation |
Score |
| 2018 |
Riaz MT, Pohorilets I, Hernandez JJ, Rios J, Totah NI. Preparation of 2-(trimethylsilyl)methyl-2-propen-1-ol derivatives by cobalt catalyzed sp2-sp3 coupling Tetrahedron Letters. 59: 2809-2812. DOI: 10.1016/J.Tetlet.2018.06.018 |
0.557 |
|
| 2015 |
Lam T, Totah NI. Studies toward the synthesis of spirastrellolide A. Preparation of a C31-C47 model Tetrahedron Letters. 56: 3349-3352. DOI: 10.1016/J.Tetlet.2015.01.026 |
0.71 |
|
| 2013 |
Liang G, Sharum DT, Lam T, Totah NI. 2-Methylenetetrahydropyrans: efficient partners in the carbonyl ene reaction. Organic Letters. 15: 5974-7. PMID 24215279 DOI: 10.1021/Ol402843S |
0.699 |
|
| 2010 |
Seth PP, Totah NI. ChemInform Abstract: Stereochemistry of the Dihydropyrone Diels-Alder Reaction. Cheminform. 31: no-no. DOI: 10.1002/chin.200005144 |
0.434 |
|
| 2009 |
Liang G, Bateman LJ, Totah NI. New reactions of 2-methylenetetrahydropyrans. A three component coupling protocol for the synthesis of tetrahydropyranyl ketides. Chemical Communications (Cambridge, England). 6457-9. PMID 19841808 DOI: 10.1039/B916190B |
0.736 |
|
| 2007 |
Teng D, Wang B, Augatis AJ, Totah NI. Studies toward the synthesis of phomactin A. An approach to the macrocyclic core. Tetrahedron Letters. 48: 4605-4607. PMID 18575571 DOI: 10.1016/J.Tetlet.2007.04.122 |
0.369 |
|
| 2005 |
Gao X, Seth PP, Bitok JK, Totah NI. An unusual intramolecular acetal alkylation Synlett. 819-823. DOI: 10.1055/S-2005-863748 |
0.501 |
|
| 2000 |
Seth PP, Totah NI. Studies toward the tricyclic core of phomactin A. Synthesis of the reduced furanochroman subunit Organic Letters. 2: 2507-2509. DOI: 10.1021/Ol0061788 |
0.543 |
|
| 2000 |
Patra D, Yang L, Totah NI. Synthesis and evaluation of new 1,7-dioxaspiro[5.5]undecane ligands: Implications for the use of diols in the desymmetrization of meso epoxides Tetrahedron. 56: 507-513. DOI: 10.1016/S0040-4020(99)01044-3 |
0.471 |
|
| 2000 |
Seth PP, Chen D, Wang J, Gao X, Totah NI. The dihydropyrone Diels-Alder reaction: Development and application to the synthesis of highly functionalized 1-oxa-4-decalones Tetrahedron. 56: 10185-10195. DOI: 10.1016/S0040-4020(00)00863-2 |
0.532 |
|
| 1999 |
Chen D, Wang J, Totah NI. Dihydropyrones as Dienophiles in the Diels-Alder Reaction: Application to the Synthesis of 1-Oxadecalones. The Journal of Organic Chemistry. 64: 1776-1777. PMID 11674261 DOI: 10.1021/Jo982488G |
0.558 |
|
| 1999 |
Seth PP, Totah NI. On the stereochemistry of the dihydropyrone Diels-Alder reaction Organic Letters. 1: 1411-1414. DOI: 10.1021/Ol9909637 |
0.531 |
|
| 1999 |
Seth PP, Totah NI. Synthesis of 1-oxadecalones via the Lewis acid catalyzed dihydropyrone Diels-Alder reaction Journal of Organic Chemistry. 64: 8750-8753. DOI: 10.1021/Jo9911746 |
0.562 |
|
| 1998 |
Totah NI, Chen D. A facile synthesis of 2,2-disubstituted 5-carbethoxy-2,3-dyhydro-4H-pyran-4-ones Tetrahedron Letters. 39: 213-216. DOI: 10.1016/S0040-4039(97)10528-7 |
0.475 |
|
| 1997 |
Eppley AW, Totah NI. A new chiral titanium species for the ring opening reactions of meso epoxides Tetrahedron. 53: 16545-16552. DOI: 10.1016/S0040-4020(97)01035-1 |
0.525 |
|
| 1996 |
Stork G, La Clair JJ, Spargo P, Nargund RP, Totah N. Stereocontrolled synthesis of (±)-12a-deoxytetracycline Journal of the American Chemical Society. 118: 5304-5305. DOI: 10.1021/Ja960434N |
0.472 |
|
| 1991 |
Totah NI, Schreiber SL. Thermodynamic spiroketalization as an efficient method of stereochemical communication The Journal of Organic Chemistry. 56: 6255-6256. DOI: 10.1021/Jo00022A003 |
0.407 |
|
| 1991 |
Totah NI, Schreiber SL. Thermodynamic spiroketalization as an efficient method of stereochemical communication Journal of Organic Chemistry. 56: 6255-6256. |
0.431 |
|
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