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Results: 1-17 |
Results: 17
An aldol approach to the synthesis of the EF fragment of spongistatin 1
Authors: Crimmins, MT Katz, JD McAtee, LC Tabet, EA Kirincich, SJ
Citation: Mt. Crimmins et al., An aldol approach to the synthesis of the EF fragment of spongistatin 1, ORG LETT, 3(6), 2001, pp. 949-952
Asymmetric aldol additions: Use of titanium tetrachloride and (-)-sparteine for the soft enolization of N-acyl oxazolidinones, oxazolidinethiones, and thiazolidinethiones
Authors: Crimmins, MT King, BW Tabet, EA Chaudhary, K
Citation: Mt. Crimmins et al., Asymmetric aldol additions: Use of titanium tetrachloride and (-)-sparteine for the soft enolization of N-acyl oxazolidinones, oxazolidinethiones, and thiazolidinethiones, J ORG CHEM, 66(3), 2001, pp. 894-902
Formal total synthesis of (+)-trehazolin. Application of an asymmetric aldol-olefin metathesis approach to the synthesis of functionalized cyclopentenes
Authors: Crimmins, MT Tabet, EA
Citation: Mt. Crimmins et Ea. Tabet, Formal total synthesis of (+)-trehazolin. Application of an asymmetric aldol-olefin metathesis approach to the synthesis of functionalized cyclopentenes, J ORG CHEM, 66(11), 2001, pp. 4012-4018
Asymmetric total synthesis of (-)-isolaurallene
Authors: Crimmins, MT Emmitte, KA
Citation: Mt. Crimmins et Ka. Emmitte, Asymmetric total synthesis of (-)-isolaurallene, J AM CHEM S, 123(7), 2001, pp. 1533-1534
Solid-phase synthesis of carbocyclic nucleosides
Authors: Crimmins, MT Zuercher, WJ
Citation: Mt. Crimmins et Wj. Zuercher, Solid-phase synthesis of carbocyclic nucleosides, ORG LETT, 2(8), 2000, pp. 1065-1067
Synthesis of the C16-C28 spiroketal subunit of spongistatin 1 (altohyrtin A): The pyrone approach
Authors: Crimmins, MT Katz, JD
Citation: Mt. Crimmins et Jd. Katz, Synthesis of the C16-C28 spiroketal subunit of spongistatin 1 (altohyrtin A): The pyrone approach, ORG LETT, 2(7), 2000, pp. 957-960
Titanium enolates of thiazolidinethione chiral auxiliaries: Versatile tools for asymmetric aldol additions
Authors: Crimmins, MT Chaudhary, K
Citation: Mt. Crimmins et K. Chaudhary, Titanium enolates of thiazolidinethione chiral auxiliaries: Versatile tools for asymmetric aldol additions, ORG LETT, 2(6), 2000, pp. 775-777
Synthesis of the C1-C13 fragment of leucascandrolide A
Authors: Crimmins, MT Carroll, CA King, BW
Citation: Mt. Crimmins et al., Synthesis of the C1-C13 fragment of leucascandrolide A, ORG LETT, 2(5), 2000, pp. 597-599
Synthesis of crossed [2+2] photocycloadducts: A novel approach to the synthesis of bridged bicyclic alkenes
Authors: Crimmins, MT Hauser, EB
Citation: Mt. Crimmins et Eb. Hauser, Synthesis of crossed [2+2] photocycloadducts: A novel approach to the synthesis of bridged bicyclic alkenes, ORG LETT, 2(3), 2000, pp. 281-284
Diastereoselective alkylations of oxazolidinone glycolates: A useful extension of the Evans asymmetric alkylation
Authors: Crimmins, MT Emmitte, KA Katz, JD
Citation: Mt. Crimmins et al., Diastereoselective alkylations of oxazolidinone glycolates: A useful extension of the Evans asymmetric alkylation, ORG LETT, 2(14), 2000, pp. 2165-2167
An efficient strategy for the synthesis of alpha,alpha'-cis and trans-disubstituted medium ring ethers
Authors: Crimmins, MT Emmitte, KA
Citation: Mt. Crimmins et Ka. Emmitte, An efficient strategy for the synthesis of alpha,alpha'-cis and trans-disubstituted medium ring ethers, SYNTHESIS-S, (6), 2000, pp. 899-903
An efficient, general asymmetric synthesis of carbocyclic nucleosides: Application of an asymmetric aldol/ring-closing metathesis strategy
Authors: Crimmins, MT King, BW Zuercher, WJ Choy, AL
Citation: Mt. Crimmins et al., An efficient, general asymmetric synthesis of carbocyclic nucleosides: Application of an asymmetric aldol/ring-closing metathesis strategy, J ORG CHEM, 65(25), 2000, pp. 8499-8509
The total synthesis of (+/-)-ginkgolide B
Authors: Crimmins, MT Pace, JM Nantermet, PG Kim-Meade, AS Thomas, JB Watterson, SH Wagman, AS
Citation: Mt. Crimmins et al., The total synthesis of (+/-)-ginkgolide B, J AM CHEM S, 122(35), 2000, pp. 8453-8463
Total Synthesis of (+)-prelaureatin and (+)-laurallene
Authors: Crimmins, MT Tabet, EA
Citation: Mt. Crimmins et Ea. Tabet, Total Synthesis of (+)-prelaureatin and (+)-laurallene, J AM CHEM S, 122(23), 2000, pp. 5473-5476
Total synthesis of (+)-laurencin: An asymmetric alkylation-ring-closing metathesis approach to medium ring ethers
Authors: Crimmins, MT Emmitte, KA
Citation: Mt. Crimmins et Ka. Emmitte, Total synthesis of (+)-laurencin: An asymmetric alkylation-ring-closing metathesis approach to medium ring ethers, ORG LETT, 1(12), 1999, pp. 2029-2032
Total synthesis of (+/-)-ginkgolide B
Authors: Crimmins, MT Pace, JM Nantermet, PG Kim-Meade, AS Thomas, JB Watterson, SH Wagman, AS
Citation: Mt. Crimmins et al., Total synthesis of (+/-)-ginkgolide B, J AM CHEM S, 121(43), 1999, pp. 10249-10250
An asymmetric aldol-ring-closing metathesis strategy for the enantioselective construction of oxygen heterocycles: An efficient approach to the enantioselective synthesis of (+)-laurencin
Authors: Crimmins, MT Choy, AL
Citation: Mt. Crimmins et Al. Choy, An asymmetric aldol-ring-closing metathesis strategy for the enantioselective construction of oxygen heterocycles: An efficient approach to the enantioselective synthesis of (+)-laurencin, J AM CHEM S, 121(24), 1999, pp. 5653-5660
Risultati: 1-17 |