N. Chandrasekhar Babu

Monoterpene

Allyl alcohol

Williamson ether synthesis

Tricyclic

10.1016/j.tet.2003.12.055

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Citations (15)

ChemInform Abstract: 1,3‐Dipolar Cycloaddition of Dipolar Reagents to Bifunctional Olefins in the Presence of Chloramine‐T (CAT).

ChemInform (2000)

V. Padmavathi R. Sumathi N. Chandrasekhar Babu D. Bhaskar Reddy

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Chloramine-T

10.1002/chin.200007054

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ChemInform Abstract: A New Method for Synthesis of 1,3,5‐Triacetylbenzene.

ChemInform (1998)

D. B. REDDY N. Chandrasekhar Babu

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

10.1002/chin.199838081

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Synthesis of sulfur‐containing heterocycles: spiropyrimidinetriones, thioxopyrimidinediones, pyrazolidinediones, and isoxazolidinediones—part ii

Heteroatom Chemistry (2001)

D. Bhaskar Reddy N. Chandrasekhar Babu V. Padmavathi

10.1002/hc.1021.abs

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Heat and Mass Transfer Studies on Unsteady Convective Flow over a Vertical Plate

N. Chandrasekhar Babu

Thesis on “Heat and Mass Transfer Studies on Unsteady Convective Flow over a Vertical Plate” submitted in partial fulfillment of the requirements for the award of the degree of Doctor Of Philosophy in Mathematics by N.V. NARENDRA BABU.

Convective flow

Degree (music)

Source

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ChemInform Abstract: Synthesis of Sulfur‐Containing Heterocycles: Spiropyrimidinetriones, Thioxopyrimidinediones, Pyrazolidinediones, and Isoxazolidinediones. Part 2.

ChemInform (2001)

D. Bhaskar Reddy N. Chandrasekhar Babu V. Padmavathi

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

10.1002/chin.200132137

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Cell Culture: An insight View

Biomedical & Pharmacology Journal (2015)

Trishna Priyadarshini N. Chandrasekhar Babu K. M. K. Masthan

10.13005/bpj/647

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A Ring Closing Metathesis Based Approach for the Spiroannulation of Cyclopentanes and Cyclohexanes. Formal Synthesis of (±)-Acorones

Synlett (2001)

A. Srikrishna M. S. Narasinga Rao Santosh J. Gharpure N. Chandrasekhar Babu

An efficient ring closing methathesis (RCM) reaction based approach was developed for the spiroannulation of cyclopentanes and cyclohexanes and its utility demonstrated in the formal synthesis of the spirosesquiterpenes acorones.

Cyclopentanes

Cyclohexanes

Ring-Closing Metathesis

Formal synthesis

10.1055/s-2001-18743

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Citations (9)

A convenient enantiospecific methodology for (-)-(1R,5S)-1,5-dimethylbicyclo[3.3.0]octa-2,7-dione: A formal total synthesis of (-)-ceratopicanol

Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry (2003)

A. Srikrishna N. Chandrasekhar Babu Dattatraya H. Dethe

An enantiospecific formal total synthesis of (-)-ceratopicanol starting from the readily and abundantly available monoterpene (R)-limonene is described. A combination of Claisen rearrangement-intramolecular diazo-ketone cyclopropanation-regiospecific reductive cyclopropane cleavage reactions are employed for the stereo- and regiospecific generation of the two vicinal ring junction quaternary carbon atoms.

Cyclopropane

Vicinal

Monoterpene

Source

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Citations (4)

Cascade Molecule: An Innovation in Nanotechnology: Review Article

Biomedical & Pharmacology Journal (2015)

S Aswini GS Asokan Vikas Anand N Balaji N. Chandrasekhar Babu

10.13005/bpj/657

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Citations (0)