Year |
Citation |
Score |
2010 |
Crich D, Smith M, Yao Q, Picione J. ChemInform Abstract: 2,4,6-Tri-tert-butylpyrimidine (TTBP): A Cost Effective, Readily Available Alternative to the Hindered Base 2,6-Di-tert-butylpyridine and Its 4-Substituted Derivatives in Glycosylation and Other Reactions. Cheminform. 32: no-no. DOI: 10.1002/chin.200124193 |
0.477 |
|
2005 |
Crich D, Vinod AU, Picione J, Wink DJ. Approximate H(5) Ring Conformation of 2,3-O-Carbonate Protected α- and β-L-Rhamnopyranosides as Confirmed by X-Ray Crystallography. Arkivoc : Free Online Journal of Organic Chemistry / Arkat-Usa, Inc. 2005: 339-344. PMID 18490964 DOI: 10.3998/Ark.5550190.0006.629 |
0.621 |
|
2005 |
Crich D, Hutton TK, Banerjee A, Jayalath P, Picione J. Disarming, non-participating 2-O-protecting groups in manno- and rhamnopyranosylation: Scope and limitations of sulfonates, vinylogous esters, phosphates, cyanates, and nitrates Tetrahedron Asymmetry. 16: 105-119. DOI: 10.1016/J.Tetasy.2004.11.032 |
0.469 |
|
2005 |
Crich D, Vinod AU, Picione J, Wink DJ. Approximate OH5 ring conformation of 2,3-O-carbonate protected α- and β-L-rhamnopyranosides as confirmed by X-ray crystallography Arkivoc. 2005: 339-344. |
0.566 |
|
2003 |
Crich D, Vinod AU, Picione J. The 3,4-O-carbonate protecting group as a beta-directing group in rhamnopyranosylation in both homogeneous and heterogeneous glycosylations as compared to the chameleon-like 2,3-O-carbonates. The Journal of Organic Chemistry. 68: 8453-8. PMID 14575470 DOI: 10.1021/Jo035003J |
0.563 |
|
2003 |
Crich D, Picione J. Direct synthesis of the beta-l-rhamnopyranosides. Organic Letters. 5: 781-4. PMID 12605514 DOI: 10.1021/Ol0340890 |
0.591 |
|
2003 |
Crich D, Picione J. 1-Benzenesulfinyl piperidine (BSP)/triflic anhydride: An effective combination for the hydrolysis of dithioacetals Synlett. 1257-1258. DOI: 10.1055/S-2003-40328 |
0.497 |
|
2003 |
Crich D, Picione J. Direct Synthesis of the β-L-Rhamnopyranosides. Cheminform. 34. DOI: 10.1002/chin.200329159 |
0.516 |
|
2001 |
Crich D, Smith M, Yao Q, Picione J. 2,4,6-Tri-tert-butylpyrimidine (TTBP): A Cost Effective, Readily Available Alternative to the Hindered Base 2,6-Di-tert-butylpyridine and its 4-Substituted Derivatives in Glycosylation and Other Reactions Synthesis. 2001: 0323-0326. DOI: 10.1055/S-2001-10798 |
0.562 |
|
2001 |
Crich D, Smith M, Yao Q, Picione J. 2,4,6-Tri-tert-butylpyrimidine (TTBP): A cost effective, readily available alternative to the hindered base 2,6-di-tert-butylpyridine and its 4-substituted derivatives in glycosylation and other reactions Synthesis. 323-326. |
0.316 |
|
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