Class information for:
Level 1: MPV TYPE REDUCTION//ZNBH42//ZINC BOROHYDRIDE

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
10845 962 24.0 46%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
766 11699 ASYMMETRIC HYDROGENATION//ASYMMETRIC TRANSFER HYDROGENATION//TRANSFER HYDROGENATION

Terms with highest relevance score


Rank Term Type of term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 MPV TYPE REDUCTION Author keyword 14 100% 1% 7
2 ZNBH42 Author keyword 11 78% 1% 7
3 ZINC BOROHYDRIDE Author keyword 10 63% 1% 10
4 MPV TYPE REACTION Author keyword 8 100% 1% 5
5 DIISOBUTYLALUMINUM HYDRIDE DIBALH Author keyword 4 75% 0% 3
6 221 TAMAGAWA CHO MINAMI KU Address 4 56% 1% 5
7 ORGANIC FUNCTIONAL GROUPS Author keyword 4 46% 1% 6
8 PARTIAL REDUCTION Author keyword 3 24% 1% 12
9 LITHIUM DIISOBUTYLPIPERIDINOHYDROALUMINATE LDBPA Author keyword 3 100% 0% 3
10 ZINC TETRAHYDROBORATE Author keyword 3 100% 0% 3

Web of Science journal categories

Author Key Words


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class		 LCSH search Wikipedia search
1 MPV TYPE REDUCTION 14 100% 1% 7 Search MPV+TYPE+REDUCTION Search MPV+TYPE+REDUCTION
2 ZNBH42 11 78% 1% 7 Search ZNBH42 Search ZNBH42
3 ZINC BOROHYDRIDE 10 63% 1% 10 Search ZINC+BOROHYDRIDE Search ZINC+BOROHYDRIDE
4 MPV TYPE REACTION 8 100% 1% 5 Search MPV+TYPE+REACTION Search MPV+TYPE+REACTION
5 DIISOBUTYLALUMINUM HYDRIDE DIBALH 4 75% 0% 3 Search DIISOBUTYLALUMINUM+HYDRIDE+DIBALH Search DIISOBUTYLALUMINUM+HYDRIDE+DIBALH
6 ORGANIC FUNCTIONAL GROUPS 4 46% 1% 6 Search ORGANIC+FUNCTIONAL+GROUPS Search ORGANIC+FUNCTIONAL+GROUPS
7 PARTIAL REDUCTION 3 24% 1% 12 Search PARTIAL+REDUCTION Search PARTIAL+REDUCTION
8 LITHIUM DIISOBUTYLPIPERIDINOHYDROALUMINATE LDBPA 3 100% 0% 3 Search LITHIUM+DIISOBUTYLPIPERIDINOHYDROALUMINATE+LDBPA Search LITHIUM+DIISOBUTYLPIPERIDINOHYDROALUMINATE+LDBPA
9 ZINC TETRAHYDROBORATE 3 100% 0% 3 Search ZINC+TETRAHYDROBORATE Search ZINC+TETRAHYDROBORATE
10 NICKEL BORIDE 2 22% 1% 10 Search NICKEL+BORIDE Search NICKEL+BORIDE

Key Words Plus


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 MODIFIED BOROHYDRIDE AGENTS 89 100% 3% 27
2 CHEMOSELECTIVE REDUCING AGENT 53 95% 2% 18
3 PYRIDINETETRAHYDROBORATOZINC COMPLEX 33 100% 1% 13
4 LIGAND METAL BOROHYDRIDE 30 100% 1% 12
5 CORRESPONDING ALLYLIC ALCOHOLS 25 77% 2% 17
6 REPRESENTATIVE FUNCTIONAL GROUPS 25 52% 4% 34
7 THEXYLBROMOBORANE DIMETHYL SULFIDE 24 91% 1% 10
8 ZINC BOROHYDRIDE 21 33% 6% 54
9 EXCEPTIONALLY FACILE REDUCTION 14 100% 1% 7
10 1 2 REDUCTION 13 80% 1% 8

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Methods of enhancement of reactivity and selectivity of sodium borohydride for applications in organic synthesis 2000 92 109 42%
Modified hydroborate agent: (2,2 '-bipyridyl)(tetrahydroborato)zinc complex, [Zn(BH4)(2)(bpy)], as a new, stable, efficient ligand-metal hydroborate and chemoselective reducing agent 2003 23 63 87%
Lithium aminoborohydrides: Powerful, selective, air-stable reducing agents 2006 16 38 66%
Recent developments in Meerwein-Ponndorf-Verley and related reactions for the reduction of organic functional groups using aluminum, boron, and other metal reagents: A review 2006 44 117 26%
Synthetically useful reactions with nickel boride. 1997 26 32 44%
Selected methods for the reduction of the azido group 2002 15 91 43%
SYNTHETICALLY USEFUL REACTIONS WITH METAL BORIDE AND ALUMINIDE CATALYSTS 1986 208 46 41%
Synthesis, characterization, and synthetic utility of lithium aminoborohydrides - A new class of powerful, selective, air-stable reducing agents 1996 2 21 76%
Selective reduction of carbonyl and epoxy compounds using aluminum, boron and other metal reagents. Comparison of reducing characteristics between the Meerwein-Ponndorf-Verley type reduction and metal complex hydrides reduction: A review 2007 6 124 23%
Use of phase-transfer catalysis in borohydride reductions: Review and new ideas 1998 1 22 41%

Address terms


Rank Address term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ.
in class
1 221 TAMAGAWA CHO MINAMI KU 4 56% 0.5% 5
2 TAMAGAWA CHO MINAMI KU 1 100% 0.2% 2
3 ORGAN 2 1 11% 0.7% 7
4 CHEM CENT UNIV PO 1 50% 0.1% 1
5 CHIM ORGAN R7 1 50% 0.1% 1
6 MED CENT UNIV PO 1 50% 0.1% 1
7 SISTESIS ORGAN 1 50% 0.1% 1
8 TECNOL FARMACOS FAR MANGUINHOS 1 10% 0.6% 6
9 CONTRACT MFG SERV 0 20% 0.2% 2
10 DR BR AMBEDKAR VEEDHI 0 33% 0.1% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000156257 REDUCTIVE AMINATION//DIRECT REDUCTIVE AMINATION//ASYMMETRIC REDUCTIVE AMINATION
2 0.0000140770 DEOXYGENATION//AMINE N OXIDES//1 AMINO 2 ACETYL ANTHRAQUINONE
3 0.0000117807 OXAZABOROLIDINE//CHIRAL OXAZABOROLIDINE//ASYMMETRIC BORANE REDUCTION
4 0.0000091205 MEERWEIN PONNDORF VERLEY REDUCTION//MPV REDUCTION//MEERWEIN PONNDORF VERLEY
5 0.0000089932 HYDROSILYLATION//COPPER HYDRIDE//TRIETHYLSILANE
6 0.0000083478 BORONIC ESTERS//HC BROWN BORANE//BORAURACIL
7 0.0000083021 ORGANOHYDROBORATE//ALUMINUM BOROHYDRIDE//CYCLIC ORGANOHYDROBORATE
8 0.0000079850 COMBINATORIAL PARALLEL MED CHEM//POLYMERIC OXIDIZING AGENT//GLAXOSMITHKLINE CAMBRIDGE TECHNOL
9 0.0000069444 STEVASTELIN//PD CEN//SEMIHYDROGENATION
10 0.0000068244 O CHLORONITROBENZENE//POLYMER SUPPORTED FORMATE//CHLORONITROBENZENE