Chiral Synthesis via Organoboranes. 40. Selective Reductions. 55. A Simple One-Pot Synthesis of the Enantiomers of Trifluoromethyloxirane. A General Synthesis in High Optical Purities of .alpha.-Trifluoromethyl Secondary Alcohols via the Ring-Cleavage Reactions of the Epoxide

P. Veeraraghavan Ramachandran; Baoqing Gong; Herbert C. Brown

doi:10.1021/jo00106a012

Chiral Synthesis via Organoboranes. 40. Selective Reductions. 55. A Simple One-Pot Synthesis of the Enantiomers of Trifluoromethyloxirane. A General Synthesis in High Optical Purities of .alpha.-Trifluoromethyl Secondary Alcohols via the Ring-Cleavage Reactions of the Epoxide

The Journal of Organic Chemistry ◽

10.1021/jo00106a012 ◽

1995 ◽

Vol 60 (1) ◽

pp. 41-46 ◽

Cited By ~ 79

Author(s):

P. Veeraraghavan Ramachandran ◽

Baoqing Gong ◽

Herbert C. Brown

Keyword(s):

Ring Cleavage ◽

Secondary Alcohols ◽

One Pot ◽

Chiral Synthesis ◽

One Pot Synthesis ◽

Cleavage Reactions ◽

General Synthesis

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ChemInform Abstract: Chiral Synthesis via Organoboranes. Part 40. Selective Reductions. Part 55. A Simple One-Pot Synthesis of the Enantiomers of ( Trifluoromethyl)oxirane. A General Synthesis in High Optical Purities of α-Trifluoromethyl Secondary Alcoho

ChemInform ◽

10.1002/chin.199527140 ◽

2010 ◽

Vol 26 (27) ◽

pp. no-no

Author(s):

P. V. RAMACHANDRAN ◽

B. GONG ◽

H. C. BROWN

Keyword(s):

One Pot ◽

Chiral Synthesis ◽

One Pot Synthesis ◽

General Synthesis

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Regioselective Hydration of Terminal Alkynes Catalyzed by a Neutral Gold(I) Complex [(IPr)AuCl] and One-Pot Synthesis of Optically Active Secondary Alcohols from Terminal Alkynes by the Combination of [(IPr)AuCl] and Cp*RhCl[(R,R)-TsDPEN]

The Journal of Organic Chemistry ◽

10.1021/acs.joc.5b00164 ◽

2015 ◽

Vol 80 (7) ◽

pp. 3538-3546 ◽

Cited By ~ 54

Author(s):

Feng Li ◽

Nana Wang ◽

Lei Lu ◽

Guangjun Zhu

Keyword(s):

Optically Active ◽

Secondary Alcohols ◽

Terminal Alkynes ◽

One Pot ◽

One Pot Synthesis

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ChemInform Abstract: Selective Rhenium-Catalyzed Oxidation of Secondary Alcohols with Methyl Sulfoxide in the Presence of Ethylene Glycol, a Convenient One-Pot Synthesis of Ketals.

ChemInform ◽

10.1002/chin.199949052 ◽

2010 ◽

Vol 30 (49) ◽

pp. no-no

Author(s):

Jeffrey B. Arterburn ◽

Marc C. Perry

Keyword(s):

Ethylene Glycol ◽

Secondary Alcohols ◽

One Pot ◽

One Pot Synthesis ◽

Methyl Sulfoxide ◽

Catalyzed Oxidation

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A novel one-pot synthesis of secondary alcohols from esters

Tetrahedron Letters ◽

10.1016/j.tetlet.2011.02.005 ◽

2011 ◽

Vol 52 (14) ◽

pp. 1718-1720 ◽

Cited By ~ 9

Author(s):

Min Jung Chae ◽

Ah Ram Jeon ◽

Jae Kyo Park ◽

Duk Keun An

Keyword(s):

Secondary Alcohols ◽

One Pot ◽

One Pot Synthesis

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ChemInform Abstract: Regioselective Hydration of Terminal Alkynes Catalyzed by a Neutral Gold(I) Complex [(IPr)AuCl] and One-Pot Synthesis of Optically Active Secondary Alcohols from Terminal Alkynes by the Combination of [(IPr)AuCl] and Cp*RhCl[(R,R)-TsD

ChemInform ◽

10.1002/chin.201534071 ◽

2015 ◽

Vol 46 (34) ◽

pp. no-no

Author(s):

Feng Li ◽

Nana Wang ◽

Lei Lu ◽

Guangjun Zhu

Keyword(s):

Optically Active ◽

Secondary Alcohols ◽

Terminal Alkynes ◽

One Pot ◽

One Pot Synthesis

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Selective Rhenium-Catalyzed Oxidation of Secondary Alcohols with Methyl Sulfoxide in the Presence of Ethylene Glycol, a Convenient One-Pot Synthesis of Ketals

Organic Letters ◽

10.1021/ol990755e ◽

1999 ◽

Vol 1 (5) ◽

pp. 769-771 ◽

Cited By ~ 21

Author(s):

Jeffrey B. Arterburn ◽

Marc C. Perry

Keyword(s):

Ethylene Glycol ◽

Secondary Alcohols ◽

One Pot ◽

One Pot Synthesis ◽

Methyl Sulfoxide ◽

Catalyzed Oxidation

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One Pot Synthesis of Chiral Secondary Alcohols using Noyori Asymmetric Transfer Hydrogenation and Williamson Monoetherification: Application in the diastereoselective Syntheses of Cis Cyclopropyl Containing Molecules

Chemical Data Collections ◽

10.1016/j.cdc.2021.100685 ◽

2021 ◽

pp. 100685

Author(s):

D.S. Ramakrishna

Keyword(s):

Transfer Hydrogenation ◽

Secondary Alcohols ◽

Asymmetric Transfer Hydrogenation ◽

One Pot ◽

One Pot Synthesis

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ChemInform Abstract: Ring Cleavage of N-Acyl- and N-(Acylsulfonyl)histamines with Di-tert-butyl Dicarbonate. A One-Pot Synthesis of 4-Acylamino- and 4-Arylsulfonylamino-1,2-diaminobutanes.

ChemInform ◽

10.1002/chin.199015271 ◽

1990 ◽

Vol 21 (15) ◽

Author(s):

A. WARSHAWSKY ◽

J. ALTMAN ◽

N. KAHANA ◽

R. ARAD-YELLIN ◽

A. DESHE ◽

...

Keyword(s):

Ring Cleavage ◽

One Pot ◽

Tert Butyl ◽

One Pot Synthesis

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A new and versatile one-pot strategy to synthesize alpha-bromoketones from secondary alcohols using ammonium bromide and oxone

New Journal of Chemistry ◽

10.1039/c7nj00052a ◽

2017 ◽

Vol 41 (10) ◽

pp. 3710-3714 ◽

Cited By ~ 5

Author(s):

Banothu Rammurthy ◽

Peraka Swamy ◽

Mameda Naresh ◽

Kodumuri Srujana ◽

Chevella Durgaiah ◽

...

Keyword(s):

Ammonium Bromide ◽

Secondary Alcohols ◽

One Pot ◽

Green Protocol ◽

One Pot Synthesis ◽

The One

A new, efficient and green protocol for the one-pot synthesis of alpha-bromoketones from secondary alcohols is reported.

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One-pot synthesis of α-iodoketones from alcohols using ammonium iodide and Oxone® in water

RSC Advances ◽

10.1039/c4ra16130k ◽

2015 ◽

Vol 5 (16) ◽

pp. 12186-12190 ◽

Cited By ~ 6

Author(s):

Marri Mahender Reddy ◽

Peraka Swamy ◽

Mameda Naresh ◽

Kodumuri Srujana ◽

Chevella Durgaiah ◽

...

Keyword(s):

Aqueous Media ◽

Secondary Alcohols ◽

Ammonium Iodide ◽

One Pot ◽

Green Protocol ◽

One Pot Synthesis

A novel and green protocol for the synthesis of α-iodoketones from various secondary alcohols in aqueous media is reported.

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