K. S. BHAT - Concepedia

Concepedia

Author

K. S. BHAT

National Chemical Laboratory

Also Known As

K. BHAT, K. Bhat, K. S. BHAT, K. S. Bhat, Krishna Bhat, Krishna S. Bhat

37

Publications

1.9K

Citations

14

H-Index

15

Concepts

All Affiliations

National Chemical Laboratory

KS

About

K. S. BHAT is an author at National Chemical Laboratory specializing in chemistry, organic chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	12	12	1.9K
2	Biomolecular Engineering	10	10	1.8K
3	Natural Sciences	9	9	1.3K
4	Biochemistry	4	4	423
5	Biostatistics	1	1	27

K. S. BHAT

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15

Publications

1.9K

Citations

14

H-Index

	Year	Citations
Chiral synthesis via organoboranes. 7. Diastereoselective and enantioselective synthesis of erythro- and threo-.beta.-methylhomoallyl alcohols via enantiomeric (Z)- and (E)-crotylboranes Herbert C. Brown, K. S. BHAT Journal of the American Chemical Society EngineeringThreo-.beta.-methylhomoallyl AlcoholsNatural SciencesDiversity-oriented SynthesisAltmetric Attention Score	1986	376
Chiral synthesis via organoboranes. 6. Asymmetric allylboration via chiral allyldialkylboranes. Synthesis of homoallylic alcohols with exceptionally high enantiomeric excess Prabhakar K. Jadhav, K. S. BHAT, Paramasivan T. Perumal, The Journal of Organic Chemistry EngineeringNatural SciencesDiversity-oriented SynthesisChiral AllyldialkylboranesAltmetric Attention Score	1986	356
Enantiomeric Z- and E-crotyldiisopinocampheylboranes. Synthesis in high optical purity of all four possible stereoisomers of .beta.-methylhomoallyl alcohols Herbert C. Brown, K. S. BHAT Journal of the American Chemical Society EngineeringDonut Icon.Beta.-methylhomoallyl AlcoholsEnantiomeric Z-Altmetric Attention Score	1986	321
Chiral synthesis via organoboranes. 21. Allyl- and crotylboration of .alpha.-chiral aldehydes with diisopinocampheylboron as the chiral auxiliary Herbert C. Brown, K. S. BHAT, Ramnarayan S. Randad The Journal of Organic Chemistry EngineeringBiochemistryNatural Sciences.Alpha.-chiral AldehydesAltmetric Attention Score	1989	220
Chiral synthesis via organoboranes. 13. A highly diastereoselective and enantioselective addition of [(Z)-.gamma.-alkoxyallyl]diisopinocampheylboranes to aldehydes Herbert C. Brown, Prabhakar K. Jadhav, K. S. BHAT Journal of the American Chemical Society EngineeringDonut IconAltmetric Attention ScoreOrganic ChemistrySocial Media Presence	1988	203
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
An asymmetric synthesis of the diastereomeric 1-(2-cyclohexenyl)-1-alkanols in high optical purity via a stereochemically stable allylic borane, B-2-cyclohexen-1-yldiisopinocampheylborane Herbert C. Brown, Prabhakar K. Jadhav, K. S. BHAT Journal of the American Chemical Society EngineeringAlkene MetathesisDonut IconNatural SciencesDiversity-oriented Synthesis	1985	70
.beta.-Allyldiisopinocampheylborane: a remarkable reagent for the diastereoselective allylboration of .alpha.-substituted chiral aldehydes Herbert C. Brown, K. S. BHAT, Ramnarayan S. Randad The Journal of Organic Chemistry Bioorganic ChemistryEngineeringRemarkable ReagentAltmetric Attention ScoreDiastereoselective Allylboration	1987	61
Hydroboration of terpenes. 10. An improved procedure for the conversion of .alpha.-pinene into .beta.-pinene in high chemical and optical yield using a combination of the Schlosser allylic metalation of .alpha.-pinene and allylborane chemistry Herbert C. Brown, M. Zaidlewicz, K. S. BHAT The Journal of Organic Chemistry Chemical EngineeringEngineeringSchlosser Allylic MetalationAlkene MetathesisDonut Icon	1989	39
A highly diastereoselective addition of [E]- and [Z]-crotyldiisopinocampheylboranes to .alpha.-substituted aldehydes H. Brown, K. S. BHAT, Ramnarayan S. Randad The Journal of Organic Chemistry .Alpha.-substituted AldehydesDerivative (Chemistry)Bioorganic ChemistryDonut IconNatural Sciences	1987	38

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