Org synth

    • [PDF File]R.A. Rodriguez EROS: vol III and IV

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      R.A. Rodriguez EROS: vol III and IV Org. Synth. Coll. Vol. 1973, 5, 93 Tet 1985, 41, 4047 Dibenzoyl Peroxide (DBP) MeCO2Me 80 °C, 24h 67% O + O O tBu O O + tBu DBP cat. 80 °C, 24h 62% DBP cat. O MeCO2 O O JACS 1988, 110, 2650 Dibromoalane MeO O MeMe MeAl(OR)2 Br2AlH MeO OH MeMe selective for more hindered JOC 1980, 45, 2005 Dibromomethane ...

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    • Organic Syntheses, Coll. Vol. 8, p.606 (1993); Vol. 65, p ...

      500 mL) to remove the THF. Washing is continued until the organic layer stays constant in volume (Note 12). Distillation (Note 10) of the organic layer under an atmosphere of nitrogen through a short

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    • [PDF File]Package ‘Synth’ - R

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      Package ‘Synth’ February 19, 2015 Version 1.1-5 Date 2014-01-26 Title Synthetic Control Group Method for Comparative Case Studies Author Jens Hainmueller <jhain@stanford.edu>and Alexis Diamond <adiamond@fas.harvard.edu>

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    • [PDF File]Chlorotitanium Enolates N- Olefins

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      5750 J. Org. Chem. 1991,56,5750-5752 has been suggested to account for the dependence of product configuration on Lewis acid stoichiometry in the reactions of aldehydes with allyl~netals.~~ Because WCl is not capable of forming a pentacoordinated 21 complex, it shows no change in selectivity as a function of equiva- lents of Lewis acid.

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    • [PDF File]orgsyn.org

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      Org. Synth. 2017, 94, 1-15 6 DOI: 10.15227/orgsyn.094.0001 removed from the 50-mL flask and the flask is immediately attached to a vacuum distillation apparatus equipped with a multiflask collector (Figure

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    • [PDF File]Organic Syntheses, Coll. Vol. 8, p.403; Vol. 65, p.183 ...

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      laboratory ozonizer see Org. Synth., Coll. Vol. III, 1955, 673. The checkers used a Welsbach Model T-408 Laboratory Ozonizer, Welsbach Corp., Philadelphia, PA. The power setting was 100 V (AC) and the oxygen pressure setting was 8 psi 0.55 kg/cm2) to produce 2–3% ozone at a gas flow rate (rotameter) of 2 L/min.

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    • [PDF File]Total Syntheses of (+)- and (–)-Pestalotiopsin A

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      S2 The following reaction was carried out under Ar. To a cooled (–25 °C) stirred solution of 3-trimethylsilylpropiolic acid1 (4.95 g, 34.8 mmol) in THF (100 mL) were added Et 3N (9.4 mL, 67 mmol) and PivCl (4.0 mL, 33 mmol).

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    • [PDF File]Organic Syntheses, Coll. Vol. 6, p.353 (1988); Vol. 59, p ...

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      CLEAVAGE OF METHYL ETHERS WITH IODOTRIMETHYLSILANE: CYCLOHEXANOL FROM CYCLOHEXYL METHYL ETHER Submitted by Michael E. Jung1 and Mark A. Lyster12. Checked by Joan Huguet, H. Shibuya, and S. Masamune. 1. Procedure A. Iodotrimethylsilane. A 250-ml., two-necked, round-bottomed flask equipped with a magnetic

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    • [PDF File]DiscussionAddendumfor:( Formationofγ4 KetoEsters(from ...

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      249 Org. Synth. 2014, 91, 248-259 A one-pot zinc carbenoid-mediated homologation reaction was reported by Zercher and co-workers.6 Treatment of unfunctionalized β-keto esters with the Furukawa-modified Simmons-Smith reagent,7 generated from an equimolar ratio …

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