Year |
Citation |
Score |
2002 |
Singleton DA, Wang Y, Yang HW, Romo D. Mechanism and origin of stereoselectivity in Lewis acid catalyzed [2 + 2] cycloadditions of ketenes with aldehydes. Angewandte Chemie (International Ed. in English). 41: 1572-5. PMID 19750669 DOI: 10.1002/1521-3773(20020503)41:9<1572::Aid-Anie1572>3.0.Co;2-B |
0.649 |
|
2002 |
Singleton DA, Wang Y, Yang HW, Romo D. Mechanism and origin of stereoselectivity in Lewis acid catalyzed [2 + 2] cycloadditions of ketenes with aldehydes Angewandte Chemie - International Edition. 41: 1572-1575. DOI: 10.1002/1521-3773(20020503)41:9<1572::AID-ANIE1572>3.0.CO;2-B |
0.649 |
|
1999 |
Yang HW, Romo D. A single-pot, mild conversion of β-lactones to β-lactams Journal of Organic Chemistry. 64: 7657-7660. DOI: 10.1021/jo990826n |
0.486 |
|
1999 |
Yang HW, Romo D. Corrigendum to Tetrahedron report number 492: “Methods for the synthesis of optically active β-lactones (2-oxetanones)” [Tetrahedron 55 (1999) 6403] Tetrahedron. 55: 9347. DOI: 10.1016/S0040-4020(99)00515-3 |
0.504 |
|
1999 |
Yang HW, Romo D. Methods for the synthesis of optically active β-lactones (2- oxetanones) Tetrahedron. 55: 6403-6434. DOI: 10.1016/S0040-4020(99)00185-4 |
0.505 |
|
1998 |
Romo D, Harrison PH, Jenkins SI, Riddoch RW, Park K, Yang HW, Zhao C, Wright GD. Synthesis and inhibitory action on HMG-CoA synthase of racemic and optically active oxetan-2-ones (beta-lactones). Bioorganic & Medicinal Chemistry. 6: 1255-72. PMID 9784867 DOI: 10.1016/S0968-0896(98)00114-X |
0.562 |
|
1998 |
Yang HW, Romo D. Practical, One-Step Synthesis of Optically Active β-Lactones via the Tandem Mukaiyama Aldol−Lactonization (TMAL) Reaction The Journal of Organic Chemistry. 63: 1344-1347. DOI: 10.1021/Jo971837O |
0.316 |
|
1998 |
Yang HW, Romo D. Studies of the asymmetric [2+2] cycloaddition of silylketenes and aldehydes employing Ti-TADDOL catalysts Tetrahedron Letters. 39: 2877-2880. DOI: 10.1016/S0040-4039(98)00422-5 |
0.524 |
|
1997 |
Yang HW, Romo D. A Highly Diastereoselective, Tandem Mukaiyama Aldol-Lactonization Route to beta-Lactones: Application to a Concise Synthesis of the Potent Pancreatic Lipase Inhibitor, (-)-Panclicin D. The Journal of Organic Chemistry. 62: 4-5. PMID 11671357 DOI: 10.1021/Jo9619488 |
0.541 |
|
1997 |
Yang HW, Romo D. A highly diastereoselective, tandem Mukaiyama aldol-lactonization route to β-lactones: Application to a concise synthesis of the potent pancreatic lipase inhibitor, (-)-panclicin D Journal of Organic Chemistry. 62: 4-5. DOI: 10.1021/jo9619488 |
0.551 |
|
1997 |
Yang HW, Zhao C, Romo D. Studies of the tandem mukaiyama aldol-lactonization (TMAL) reaction: A concise and highly diastereoselective route to β-lactones applied to the total synthesis of the potent pancreatic lipase inhibitor, (-)-Panclicin D Tetrahedron. 53: 16471-16488. DOI: 10.1016/S0040-4020(97)01029-6 |
0.62 |
|
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