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Dive into the research topics where G. Venkat Rao is active.

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Featured researches published by G. Venkat Rao.


Tetrahedron Letters | 1999

A novel, simple, chemoselective and practical protocol for the reduction of azides using In/NH4Cl

G.Vidyasagar Reddy; G. Venkat Rao; D.S. Iyengar

Abstract A simple, mild and efficient method for the reduction of azides to amines using In/NH 4 Cl is described.


Synthetic Communications | 2000

A New Novel and Practical One Pot Methodology for Conversion of Alcohols to Amines

G. Vidya Sagar Reddy; G. Venkat Rao; R. V. K. Subramanyam; D. S. Iyengar

Abstract A convenient and efficient one pot sequence has been developed for the transformation of alcohols to amines using Sodium azide, triphenylphosphine in CC14-DMF.


Tetrahedron Letters | 1998

A practical approach for the optically pure N-Methyl-α-amino acids

G.Vidyasagar Reddy; G. Venkat Rao; D.S. Iyengar

Abstract A new practical synthesis of N-Methyl-α-amino acids by racemization free methodology has been developed. The method involves the reductive cleavage of N-protected oxazolidinones using hydrogen in the presence of Pd C to give the title compounds in quantitative yields.


Tetrahedron Letters | 1999

A novel Wittig reaction of oxazolidinones: Stereospecific synthesis of N-BOC-(3S,4S)-Statine and N-BOC-(3S,4S)-AHPPA

G.Vidyasagar Reddy; G. Venkat Rao; D.S. Iyengar

Abstract Stereospecific synthesis of N-BOC-(3 S ,4 S )-Statine and N-BOC-(3 S ,4 S )-AHPPA is achieved via a novel Wittig reaction of oxazolidinones in an efficient manner.


Tetrahedron Letters | 2000

An enantioselective synthesis of (1S,2S)-pseudoephedrine†

G.Vidyasagar Reddy; G. Venkat Rao; V Sreevani; D. S. Iyengar

Synthesis of (1S,2S)-pseudoephedrine is described via reduction of an alanine-derived oxazolidinone followed by treating with phenyl magnesium bromide and chemoselective N-methylation in an efficient and practical manner.


Tetrahedron Letters | 1999

SELECTIVE REDUCTIONS OF OXAZOLIDINONES : NEW PROTOCOL FOR DIASTEREOSELECTIVE SYNTHESIS OF VICINAL AMINO ALCOHOLS

G.Vidyasagar Reddy; G. Venkat Rao; D.S. Iyengar

Abstract Selective reductions of oxazolidinones using sodium borohydride and their application to the diastereoselective synthesis of vicinal amino alcohols are described.


Synthetic Communications | 1999

A Novel, Simple and Rapid Protocol For N-Protected-oxazolidine-5-ones

G.Vidyasagar Reddy; G. Venkat Rao; D. S. Iyengar

Abstract A simple and efficient method for the preparation of N-protected oxazolidine-5-ones using microwave irradiation is described.


Synthetic Communications | 2000

A Novel, Practical and Highly Chemoselective Methodology for Reduction of Disulphides to Thiols

G. Vidya Sagar Reddy; G. Venkat Rao; D. S. Iyengar

Abstract A novel, simple and efficient method for the reduction of disulfides to thiols using In/NH4Cl is described.


Synthetic Communications | 2000

A Novel, Simple and Rapid Regeneration of Alcohols from Their Allylic Ethers Using NaCNBH3 / TMSCl

G. Venkat Rao; D. Subhash Reddy; G. Hari Mohan; D. S. Iyengar

Abstract A Novel, Simple and efficient method for the regeneration of alcohols from their allylic ethers using NaCNBH3/TMSCl is described.


Tetrahedron Letters | 2000

A practical protocol for chemoselective N-methylation of vicinal amino alcohols

G.Vidyasagar Reddy; G. Venkat Rao; V Sreevani; D. S. Iyengar

Abstract A practical method for the chemoselective N-methylation of vicinal amino alcohols is described.

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D. S. Iyengar

Indian Institute of Chemical Technology

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G.Vidyasagar Reddy

Indian Institute of Chemical Technology

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D.S. Iyengar

Indian Institute of Chemical Technology

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V Sreevani

Indian Institute of Chemical Technology

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G. Vidya Sagar Reddy

Indian Institute of Chemical Technology

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D. Subhash Reddy

Indian Institute of Chemical Technology

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G. Hari Mohan

Indian Institute of Chemical Technology

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R. V. K. Subramanyam

Indian Institute of Chemical Technology

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