Year |
Citation |
Score |
2010 |
O'Malley SJ, Leighton JL. ChemInform Abstract: Tandem Intramolecular Alkyne Silylformylation-Allylsilylation: A Case of Remote 1,5-Asymmetric Induction. Cheminform. 32: no-no. DOI: 10.1002/chin.200147049 |
0.598 |
|
2008 |
Watzke A, Wilson RM, O'Malley SJ, Bergman RG, Ellman JA. ChemInform Abstract: Asymmetric Intramolecular Alkylation of Chiral Aromatic Imines via Catalytic C—H Bond Activation. Cheminform. 39. DOI: 10.1002/chin.200805100 |
0.337 |
|
2006 |
Watzke A, O'Malley SJ, Bergman RG, Ellman JA. Reassignment of the configuration of salvianolic acid B and establishment of its identity with lithospermic acid B. Journal of Natural Products. 69: 1231-3. PMID 16933885 DOI: 10.1021/Np060136W |
0.435 |
|
2006 |
Park PK, O'Malley SJ, Schmidt DR, Leighton JL. Total synthesis of dolabelide D Journal of the American Chemical Society. 128: 2796-2797. PMID 16506747 DOI: 10.1021/Ja058692K |
0.57 |
|
2005 |
O'Malley SJ, Tan KL, Watzke A, Bergman RG, Ellman JA. Total synthesis of (+)-lithospermic acid by asymmetric intramolecular alkylation via catalytic C-H bond activation. Journal of the American Chemical Society. 127: 13496-7. PMID 16190703 DOI: 10.1021/Ja052680H |
0.565 |
|
2003 |
Schmidt DR, O'Malley SJ, Leighton JL. Catalytic asymmetric silane alcoholysis: Practical access to chiral silanes Journal of the American Chemical Society. 125: 1190-1191. PMID 12553820 DOI: 10.1021/Ja0283201 |
0.637 |
|
2003 |
Zacuto MJ, O'Malley SJ, Leighton JL. Tandem silylformylation-allyl(crotyl)silylation: A new approach to polyketide synthesis Tetrahedron. 59: 8889-8900. DOI: 10.1016/J.Tet.2003.04.004 |
0.663 |
|
2002 |
Zacuto MJ, O'Malley SJ, Leighton JL. Tandem intramolecular silylformylation-crotylsilylation: Highly efficient synthesis of polyketide fragments Journal of the American Chemical Society. 124: 7890-7891. PMID 12095319 DOI: 10.1021/Ja026511Y |
0.67 |
|
2001 |
O'Malley SJ, Leighton JL. Tandem Intramolecular Alkyne Silylformylation-Allylsilylation: A Case of Remote 1,5-Asymmetric Induction. Angewandte Chemie (International Ed. in English). 40: 2915-2917. PMID 29711987 DOI: 10.1002/1521-3773(20010803)40:15<2915::Aid-Anie2915>3.0.Co;2-9 |
0.687 |
|
2001 |
O'Malley SJ, Leighton JL. Tandem Intramolecular Alkyne Silylformylation-Allylsilylation: A Case of Remote 1,5-Asymmetric Induction Financial support was provided by the National Institutes of Health (National Institute of General Medical Sciences, GM58133). We are grateful to Bristol-Myers Squibb for generous financial support in the form of an Unrestricted Grant in Synthetic Organic Chemistry to J.L.L. We thank Merck Research Laboratories and DuPont Pharmaceuticals for generous financial support. Angewandte Chemie (International Ed. in English). 40: 2915-2917. PMID 11500908 DOI: 10.1002/1521-3773(20010803)40:15<2915::AID-ANIE2915>3.0.CO;2-9 |
0.49 |
|
2001 |
O'Malley SJ, Leighton JL. Tandem intramolecular alkyne silylformylation-allylsilylation: A case of remote 1,5-asymmetric induction Angewandte Chemie - International Edition. 40: 2915-2917. DOI: 10.1002/1521-3773(20010803)40:15<2915::AID-ANIE2915>3.0.CO;2-9 |
0.592 |
|
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