About: Bhalchandra Bhanage

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

chemistry researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) باحت (ary) изилдөөчү (ky) 研究者 (zh) chemistry researcher (en)
rdfs:label	Bhalchandra Bhanage (en) Bhalchandra Bhanage (es) Bhalchandra Bhanage (nl) Bhalchandra Bhanage (ast) Bhalchandra M. Bhanage (cs)
skos:prefLabel	Bhalchandra Bhanage (en) Bhalchandra Bhanage (es) Bhalchandra Bhanage (nl) Bhalchandra Bhanage (ast) Bhalchandra M. Bhanage (cs)
name	Bhalchandra Bhanage (en) Bhalchandra Bhanage (es) Bhalchandra Bhanage (nl) Bhalchandra Bhanage (ast) Bhalchandra M. Bhanage (cs)
Scopus author ID	wds:Q57687984-85228C0B-A3BD-4A66-9494-57EB2BD75311
Scopus author ID	7003303262
instance of	wds:Q57687984-18FCF177-AE2F-48C8-BB0F-7ED51CE1F4A8
NL CR AUT ID	wds:q57687984-90bec99b-42d9-584e-51e6-d938b13f3bf0
instance of	Homo sapiens
NL CR AUT ID	ntk2014838937
Google Scholar author ID	wds:Q57687984-a488f174-47fd-69c2-b0bb-166565f79b23
Google Scholar author ID	Z0EZnv8AAAAJ
skos:altLabel	Bhalchandra M. Bhanage (en)
occupation	wds:Q57687984-C7979F0C-003F-44C6-AEA2-98FFD64475C5
employer	wds:Q57687984-99F8DDDE-3E60-4828-A608-2153168A0A0D wds:Q57687984-E7E6EEC3-247D-4B6A-A264-1AC14A2C5B88
CiNii Research ID	wds:Q57687984-A5237233-E4CE-4004-BD6F-60D130D4F986
NUKAT ID	wds:Q57687984-1433ABA0-8D78-4A90-9107-F944C85BF485
sex or gender	wds:Q57687984-D0DF13EC-7C2F-4EF4-BE36-BBCD318BE0FB
VIAF ID	wds:Q57687984-C246C838-909A-45B6-B6AF-7CEF48DC55C1
GND ID	wds:Q57687984-95eb0f2d-af7c-4545-87c4-84e4122d0cd5
Library of Congress authority ID	wds:Q57687984-D06EAA20-6EA5-40A2-BC56-9DAE1B924572
NACSIS-CAT author ID	wds:q57687984-8de50499-42ad-a2b9-e1ee-c02b936c9016
educated at	wds:Q57687984-363842A8-E4B1-4FF3-8EAA-27999FA767D0
WorldCat Identities ID (superseded)	wds:Q57687984-DCF76D58-9E95-4082-9E9B-63238E9562ED
Canadiana Name Authority ID	wds:q57687984-523fec12-41e9-9741-02bd-bda26465a333
official website	wds:Q57687984-322EE965-69F2-4723-BBA7-95D8E774A18A
CiNii Research ID	https://cir.nii.ac.jp/crid/1140563741730180224.rdf
VIAF ID	http://viaf.org/viaf/307307563
GND ID	https://d-nb.info/gnd/1049263952
Library of Congress authority ID	http://id.loc.gov/authorities/names/no2024006261
NACSIS-CAT author ID	https://ci.nii.ac.jp/author/DA18426498#entity
occupation	researcher
employer	Institute of Chemical Technology National Chemical Laboratory
CiNii Research ID	1140563741730180224
NUKAT ID	n2014092383
sex or gender	male
VIAF ID	307307563
GND ID	1049263952
Library of Congress authority ID	no2024006261
NACSIS-CAT author ID	DA18426498
educated at	National Chemical Laboratory
WorldCat Identities ID (superseded)	viaf-307307563
Canadiana Name Authority ID	ncf11653196
official website	http://bmbhanage.weebly.com/
ORCID iD	wds:Q57687984-83F8DCE1-0584-47F7-B31F-406640B3C7F4
ORCID iD	https://orcid.org/0000-0001-9538-3339
ORCID iD	0000-0001-9538-3339
ResearcherID	wds:Q57687984-7fee6695-4132-00e5-fcc3-79b235e90b9b
ResearcherID	Y-1827-2019
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57687984
is author of	Synthesis of quinazolines from 2-aminobenzylamines with benzylamines and N-substituted benzylamines under transition metal-free conditions. Amine-Functionalized Graphene Oxide-Stabilized Pd Nanoparticles (Pd@APGO): A Novel and Efficient Catalyst for the Suzuki and Carbonylative Suzuki-Miyaura Coupling Reactions Brønsted acidity of protic ionic liquids: a modern ab initio valence bond theory perspective. An Electrochemical Method for Carboxylic Ester Synthesis from N-Alkoxyamides. iEDDA Reaction of the Molecular Iodine-Catalyzed Synthesis of 1,3,5-Triazines via Functionalization of the sp3 C-H Bond of Acetophenones with Amidines: An Experimental Investigation and DFT Study. Room-Temperature Asymmetric Transfer Hydrogenation of Biomass-Derived Levulinic Acid to Optically Pure γ-Valerolactone Using a Ruthenium Catalyst Ru-Catalyzed asymmetric transfer hydrogenation of substituted dibenzo[b,f][1,4]oxazepines in water. Immobilized lipase catalyzed synthesis of n -amyl acetate: parameter optimization, heterogeneous kinetics, continuous flow operation and reactor modeling Synthesis of Ethylene Glycol from Syngas via Oxidative Double Carbonylation of Ethanol to Diethyl Oxalate and Its Subsequent Hydrogenation N-Tosylhydrazone directed annulation via C–H/N–N bond activation in Ru(ii)/PEG-400 as homogeneous recyclable catalytic system: a green synthesis of isoquinolines Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and Suzuki-Miyaura Cross-Coupling with High Catalytic Turnovers Kinetic Resolution Driven Diastereo- and Enantioselective Synthesis of cis-β-Heteroaryl Amino Cycloalkanols by Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation tert-Butyl Nitrite-Mediated Synthesis of N-Nitrosoamides, Carboxylic Acids, Benzocoumarins, and Isocoumarins from Amides. Combining Electronic and Steric Effects To Generate Hindered Propargylic Alcohols in High Enantiomeric Excess. Highly Enantioselective One-Pot Synthesis of Chiral β-Heterosubstituted Alcohols via Ruthenium–Prolinamide-Catalyzed Asymmetric Transfer Hydrogenation Cp*Co(iii)-catalyzed annulation of azines by C-H/N-N bond activation for the synthesis of isoquinolines
is author of	wds:Q92940871-F20E68B8-4241-436C-9950-D0D2A0C29A6D wds:Q48129710-ED1A0BCB-C60D-4473-906C-88F1F962B359 wds:Q48312069-FC09B2AC-CE2F-457E-9F0B-F3FC0B0B8D53 wds:Q48280612-8CE38185-7DDF-4C16-8AC8-228AB13C92F9 wds:Q50216926-686E54A6-8CB9-449D-BDC5-CC83AE63A5C8 wds:Q91431342-6109A452-85C9-4C88-A8F6-2CFE8E637EEE wds:Q48005522-980486E9-7D28-4AB8-ABDB-5C939BA1E2BF wds:Q57717111-7CBFF12D-5754-4BEF-BBE4-CE994731740F wds:Q57717112-F5DF849C-5E37-44C8-AD4E-F704952DD8DE

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