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Dive into the research topics where Mahesh L. Patil is active.

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Featured researches published by Mahesh L. Patil.


Organic Letters | 2010

Enantioselective Wacker-type cyclization of 2-alkenyl-1,3-diketones promoted by Pd-SPRIX catalyst.

Kazuhiro Takenaka; Mohanta Sc; Mahesh L. Patil; Rao Cv; Shinobu Takizawa; Takeyuki Suzuki; Hiroaki Sasai

An enantioselective intramolecular Wacker-type cyclization of 2-alkenyl-1,3-diketones catalyzed by a Pd(II)-SPRIX complex was developed. The reaction proceeded in a 6-endo-trig mode to give the desired chromene derivatives with moderate to good enantioselectivity. Isomerization of C-C double bonds via a pi-allyl Pd intermediate was involved as the key step.


Chemical Record | 2008

Recent developments on chiral ionic liquids: design, synthesis, and applications.

Mahesh L. Patil; Hiroaki Sasai

The recent progress in chiral ionic liquids with respect to their syntheses and applications in enantioselective reactions and chiral recognition is described. In addition to the conventional chiral ionic liquids derived from chiral natural products, a library of novel chiral spiro compounds, including spiro bis(pyridinium) and spiro bis(imidazolium) salt, is also described.


Tetrahedron | 2002

Total synthesis of (±)-brasiliquinone B

Mahesh L. Patil; Hanumant B. Borate; Datta E. Ponde; Vishnu H. Deshpande

Abstract The total synthesis of (±)-brasiliquinone B has been achieved via a Friedel–Crafts alkylation approach. In contrast, a Friedel–Crafts acylation approach for the synthesis of (±)-brasiliquinone B resulted in formation of A ring aromatized tetracyclic products.


Tetrahedron Letters | 1999

First total synthesis of (±)-brasiliquinone B

Mahesh L. Patil; Hanumant B. Borate; Datta E. Ponde; Baburao M. Bhawal; Vishnu H. Deshpande

Abstract Brasiliquinone B (2) was synthesized from 7-methoxy-1-tetralone in 8 steps making use of Friedel-Crafts alkylation as a key step.


Heterocycles | 2005

Spiro Crown Ethers Bearing (S)-1,1'-Spirobiindanes as Chiral Backbones

Kohji Yonezawa; Mahesh L. Patil; Hiroaki Sasai; Shinobu Takizawa

The synthesis of spiro chiral crown ethers ((S)-1a) and ((S)-1b) has been achieved. The combination of (S)-1a and KOH promoted the asymmetric alkylation of glycine derivative (2) with moderate enantioselectivity.


Journal of Chemical Research-s | 2005

The synthesis of substituted tetrahydro-1H-xanthen-1-ones and xanthenes

Mahesh L. Patil; Hanumant B. Borate

A short and an efficient methodology for the synthesis of substituted tetrahydro-1H-1-xanthenones and xanthenes is described.


Tetrahedron Letters | 1999

First total synthesis of the antitumor antibiotic (±)-resorthiomycin

Datta E. Ponde; S. Ramalingam; Mahesh L. Patil; Hanumant B. Borate; Vishnu H. Deshpande

Abstract The first total synthesis of (±)-resorthiomycin, an antitumor antibiotic has been achieved.


Organic Letters | 2006

Design and synthesis of novel chiral spiro ionic liquids.

Mahesh L. Patil; Rao Cv; Yonezawa K; Shinobu Takizawa; Kiyotaka Onitsuka; Hiroaki Sasai


Tetrahedron-asymmetry | 2010

Enantioselective 6-endo-trig Wacker-type cyclization of 2-geranylphenols: application to a facile synthesis of (―)-cordiachromene

Kazuhiro Takenaka; Yugo Tanigaki; Mahesh L. Patil; C.V. Laxman Rao; Shinobu Takizawa; Takeyuki Suzuki; Hiroaki Sasai


Tetrahedron | 2007

Development of new methods toward efficient immobilization of chiral catalysts

Shinobu Takizawa; Mahesh L. Patil; Kazuyoshi Marubayashi; Hiroaki Sasai

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Hanumant B. Borate

Southern Methodist University

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