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Lautens, Mark, Rovis, Tomislav (1997) A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes. Journal Of The American Chemical Society, 119 (45) 11090-11091 doi:10.1021/ja971770m

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Reference TypeJournal (article/letter/editorial)
TitleA New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes
JournalJournal Of The American Chemical Society
AuthorsLautens, MarkAuthor
Rovis, TomislavAuthor
Year1997 (November)Volume119
Issue45
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja971770mSearch in ResearchGate
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Mindat Ref. ID1521805Long-form Identifiermindat:1:5:1521805:0
GUID0
Full ReferenceLautens, Mark, Rovis, Tomislav (1997) A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes. Journal Of The American Chemical Society, 119 (45) 11090-11091 doi:10.1021/ja971770m
Plain TextLautens, Mark, Rovis, Tomislav (1997) A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes. Journal Of The American Chemical Society, 119 (45) 11090-11091 doi:10.1021/ja971770m
In(1997, November) Journal Of The American Chemical Society Vol. 119 (45) American Chemical Society (ACS)

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Lautens, Mark, Ma, Shihong, Chiu, Pauline (1997) Synthesis of Cyclohexenols and Cycloheptenols via the Regioselective Reductive Ring Opening of Oxabicyclic Compounds. Journal Of The American Chemical Society, 119 (28) 6478-6487 doi:10.1021/ja964361j
Lautens, Mark, Fagnou, Keith, Rovis, Tomislav (2000) Rhodium-Catalyzed Asymmetric Alcoholysis and Aminolysis of Oxabenzonorbornadiene:  A New Enantioselective Carbon−Heteroatom Bond Forming Process. Journal Of The American Chemical Society, 122 (23) 5650-5651 doi:10.1021/ja000134c
Kerr, Mark S., Rovis, Tomislav (2004) Enantioselective Synthesis of Quaternary Stereocenters via a Catalytic Asymmetric Stetter Reaction. Journal Of The American Chemical Society, 126 (29) 8876-8877 doi:10.1021/ja047644h
Lautens, Mark, Kumanovic, Sophie (1995) A New Strategy to Bicyclo[5.3.0]decenes via Anionic Intramolecular Ring Opening of Oxabicyclo[3.2.1] Compounds. Journal Of The American Chemical Society, 117 (7) 1954-1964 doi:10.1021/ja00112a008
Lautens, Mark, Chiu, Pauline, Ma, Shihong, Rovis, Tomislav (1995) Nickel-Catalyzed Hydroalumination of Oxabicyclic Alkenes. Ligand Effects on the Regio- and Enantioselectivity. Journal Of The American Chemical Society, 117 (1) 532-533 doi:10.1021/ja00106a062
Lautens, Mark, Renaud, Jean-Luc, Hiebert, Sheldon (2000) Palladium-Catalyzed Enantioselective Alkylative Ring Opening. Journal Of The American Chemical Society, 122 (8) 1804-1805 doi:10.1021/ja993427i
Lautens, Mark, Fagnou, Keith, Yang, Dingqiao (2003) Rhodium-Catalyzed Asymmetric Ring Opening Reactions of Oxabicyclic Alkenes:  Application of Halide Effects in the Development of a General Process. Journal Of The American Chemical Society, 125 (48) 14884-14892 doi:10.1021/ja034845x
Lautens, Mark, Fagnou, Keith (2001) Effects of Halide Ligands and Protic Additives on Enantioselectivity and Reactivity in Rhodium-Catalyzed Asymmetric Ring-Opening Reactions. Journal Of The American Chemical Society, 123 (29) 7170-7171 doi:10.1021/ja010262g
Kerr, Mark S., Read de Alaniz, Javier, Rovis, Tomislav (2002) A Highly Enantioselective Catalytic Intramolecular Stetter Reaction. Journal Of The American Chemical Society, 124 (35) 10298-10299 doi:10.1021/ja027411v
White, Nicholas A., Rovis, Tomislav (2015) Correction to “Oxidatively Initiated NHC-Catalyzed Enantioselective Synthesis of 3,4-Disubstituted Cyclopentanones from Enals”. Journal Of The American Chemical Society, 137 (40) 13210 doi:10.1021/jacs.5b09675
Williams, Catherine M., Johnson, Jeffrey B., Rovis, Tomislav (2008) Nickel-Catalyzed Reductive Carboxylation of Styrenes Using CO2. Journal Of The American Chemical Society, 130 (45) 14936-14937 doi:10.1021/ja8062925
 
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