Uday S. Racherla - Concepedia

Author

Uday S. Racherla

Purdue University West Lafayette ORCID

Also Known As

U. S. RACHERLA, Uday Racherla, Uday S. Racherla, Uday Shanker Racherla

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Purdue University West Lafayette

About

Uday S. Racherla is an author at Purdue University West Lafayette specializing in engineering, organic chemistry, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	18	28	1.8K
2	Natural Sciences	11	11	972
3	Biochemistry	9	9	829
4	Business	1	1	28
5	Management	1	1	28

Uday S. Racherla

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Chiral synthesis via organoboranes. 27. Remarkably rapid and exceptionally enantioselective (approaching 100% ee) allylboration of representative aldehydes at -100.degree. under new, salt-free conditions Uday S. Racherla, Herbert C. Brown The Journal of Organic Chemistry HalogenationSalt-free ConditionsEnantioselective SynthesisEngineeringBiochemistry	1991	356
Efficient manganese catalysts for low-temperature bleaching Ronald Hage, Jan E. Iburg, Judith L. Kerschner, Nature Chemical EngineeringCatalytic ApplicationEngineeringEfficient Manganese CatalystsCatalyst Recycling	1994	335
Organoboranes. 53. A high-field variable-temperature proton and boron-11 NMR study of the effects of solvent and structure on reactivity in allylboration Herbert C. Brown, Uday S. Racherla, Perry J. Pellechia The Journal of Organic Chemistry Chemical EngineeringMolecular SciencesHigh-field Variable-temperature ProtonEngineeringBiochemistry	1990	130
Chiral synthesis via organoboranes. 24. B-allylbis(2-isocaranyl)borane as a superior reagent for the asymmetric allylboration of aldehydes Herbert C. Brown, Ramnarayan S. Randad, K. S. BHAT, Journal of the American Chemical Society Asymmetric AllylborationEngineeringBiochemistryNatural SciencesAltmetric Attention Score	1990	123
Organoboranes. 44. A convenient, highly efficient synthesis of triorganylboranes via a modified organometallic route Herbert C. Brown, Uday S. Racherla The Journal of Organic Chemistry Novel OrganocatalystsEngineeringBiochemistryNatural SciencesAltmetric Attention Score	1986	108
Chiral Synthesis via Organoboranes. 39. A Facile Synthesis of .gamma.-Substituted-.gamma.-butyrolactones in Exceptionally High Enantiomeric Purity Herbert C. Brown, Shekhar V. Kulkarni, Uday S. Racherla The Journal of Organic Chemistry EngineeringDonut IconNatural SciencesFacile SynthesisDiversity-oriented Synthesis	1994	100
Improved highly efficient synthesis of α,β-acetylenic ketones. Nature of the intermediate from the reaction of lithium acetylide with boron trifluoride etherate Herbert C. Brown, Uday S. Racherla, Shankar M. Singh, Tetrahedron Letters Engineeringβ-Acetylenic KetonesLithium AcetylideOrganic ChemistryCatalysis	1984	82
Chiral synthesis via organoboranes. 36. Exceptionally enantioselective allylborations of representative heterocyclic aldehydes at -100 .degree.C under salt-free conditions Uday S. Racherla, Yi Liao, Herbert C. Brown The Journal of Organic Chemistry Salt-free ConditionsChemical EngineeringEngineeringHeterocyclic-100 .Degree.c	1992	78
Chiral synthesis via organoboranes. 35. Simple procedures for the efficient recycling of the terpenyl chiral auxiliaries and convenient isolation of the homoallylic alcohols in asymmetric allyl- and crotylboration of aldehydes Herbert C. Brown, Uday S. Racherla, Youqiang Liao, The Journal of Organic Chemistry EngineeringDonut IconSimple ProceduresAltmetric Attention ScoreTerpenyl Chiral Auxiliaries	1992	55
Organoboranes. 38. A facile and highly efficient addition of B-1-alkynyl-9-borabicyclo[3.3.1]nonanes to aldehydes and ketones: an exceptionally chemoselective synthesis of propargylic alcohols Herbert C. Brown, Gary A. Molander, Shankar M. Singh, The Journal of Organic Chemistry Chemoselective SynthesisEngineeringNatural SciencesDiversity-oriented SynthesisPropargylic Alcohols	1985	43

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