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Dive into the research topics where D. S. Iyengar is active.

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Featured researches published by D. S. Iyengar.


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.


Synthetic Communications | 1997

Regioselective Cleavage of Epoxides: Conversion of Racemic Epoxides to Optically Active Alcohols

Y. R. Santosh Laxmi; D. S. Iyengar

Abstract Regioselective reduction of racemic epoxides to optically active alcohols using chirally modified zirconium tetrachloride - sodium borohydride with L-proline.


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.


Synthetic Communications | 1999

Reductive Cleavage of Acetals/Ketals with ZrCl4/NaBH4

K. Purushothama Chary; Y. R. Santosh Laxmi; D. S. Iyengar

Abstract Reductive cleavage of acetals/ketals with zirconium tetrachloride-sodium borohydride leading to the formation of ether alcohols is described.


Synthetic Communications | 2007

A Rapid and Efficient Cleavage of Organic Disulfides to Mercaptans Using ZrCl4/NaBH4

K. Purushothama Chary; S. Rajaram; D. S. Iyengar

Abstract A practical & cheaper reagent system ZrCl4/NaBH4 is used for the reductive cleavage of organic disulfides to mercaptans under mild conditions, in excellent yields.


Synthetic Communications | 2000

An Efficient and Selective Deprotection of Tetrahydropyranyl Ethers by CeCl3.7H2O

G. Sudhakar Reddy; Paravathi Neelakantan; D. S. Iyengar

Abstract Treatment of tetrahydropyranyl ethers with cerium (III) chloride heptahydrate in methanol provides a simple, convenient and selective method for detetrahydropyranylation, and the parent alcohols are obtained in high yields.


Synthetic Communications | 2000

An Efficient and Chemoselective Deoxygenation of Hetero Cyclic N-Oxides Using Licl/nabh4

S. Raja Ram; K. Purushothama Chary; D. S. Iyengar

Abstract A practical & novel reagent system L1C1/NaBH4 is used for the deoxygenation of N-Oxides to amines is 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, Chemoselective and Efficient Production of Amines from Azides Using ZrCl4/NaBH4

K. Purushothama Chary; S. Raja Ram; S. Salahuddin; D. S. Iyengar

Abstract A practical & cheaper reagent system ZrCl4/NaBH4 is used for the production of amines from azldes is described.

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G. Sudhakar Reddy

Indian Institute of Chemical Technology

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G. Venkat Rao

Indian Institute of Chemical Technology

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K. Purushothama Chary

Indian Institute of Chemical Technology

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Parvathi Neelakantan

Indian Institute of Chemical Technology

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S. Raja Ram

Indian Institute of Chemical Technology

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G. Hari Mohan

Indian Institute of Chemical Technology

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G.Vidyasagar Reddy

Indian Institute of Chemical Technology

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S. Salahuddin

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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