Class information for:
Level 1: MITSUNOBU REACTION//THIO MITSUNOBU REACTION//MITSUNOBU

Basic class information

ID Publications Average number
of references
Avg. shr. active
ref. in WoS
15969 613 27.2 59%



Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)



ID, lev.
above
Publications Label for level above
977 10140 JOURNAL OF COMBINATORIAL CHEMISTRY//SOLID PHASE SYNTHESIS//NATIVE CHEMICAL LIGATION

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 MITSUNOBU REACTION Author keyword 7 11% 9% 58
2 THIO MITSUNOBU REACTION Author keyword 6 80% 1% 4
3 MITSUNOBU Author keyword 3 21% 2% 14
4 OXIDATION REDUCTION CONDENSATION Author keyword 3 60% 0% 3
5 H DIMETHYLPHOSPHONATE Author keyword 2 67% 0% 2
6 HENDRICKSON REAGENT Author keyword 2 50% 0% 3
7 MITSUNOBU REACTIONS Author keyword 2 19% 1% 7
8 1 3 2 LAMBDA5 DIOXAPHOSPHOLANES Author keyword 1 100% 0% 2
9 AZO REAGENT Author keyword 1 100% 0% 2
10 CMMP Author keyword 1 100% 0% 2

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 MITSUNOBU REACTION 7 11% 9% 58 Search MITSUNOBU+REACTION Search MITSUNOBU+REACTION
2 THIO MITSUNOBU REACTION 6 80% 1% 4 Search THIO+MITSUNOBU+REACTION Search THIO+MITSUNOBU+REACTION
3 MITSUNOBU 3 21% 2% 14 Search MITSUNOBU Search MITSUNOBU
4 OXIDATION REDUCTION CONDENSATION 3 60% 0% 3 Search OXIDATION+REDUCTION+CONDENSATION Search OXIDATION+REDUCTION+CONDENSATION
5 H DIMETHYLPHOSPHONATE 2 67% 0% 2 Search H+DIMETHYLPHOSPHONATE Search H+DIMETHYLPHOSPHONATE
6 HENDRICKSON REAGENT 2 50% 0% 3 Search HENDRICKSON+REAGENT Search HENDRICKSON+REAGENT
7 MITSUNOBU REACTIONS 2 19% 1% 7 Search MITSUNOBU+REACTIONS Search MITSUNOBU+REACTIONS
8 1 3 2 LAMBDA5 DIOXAPHOSPHOLANES 1 100% 0% 2 Search 1+3+2+LAMBDA5+DIOXAPHOSPHOLANES Search 1+3+2+LAMBDA5+DIOXAPHOSPHOLANES
9 AZO REAGENT 1 100% 0% 2 Search AZO+REAGENT Search AZO+REAGENT
10 CMMP 1 100% 0% 2 Search CMMP Search CMMP

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 2 6 DIMETHYL 1 4 BENZOQUINONE 23 79% 2% 15
2 DIETHYL AZODICARBOXYLATE 17 24% 10% 63
3 ESTERIFICATION REACTION 17 41% 5% 32
4 CYCLIC PHOSPHORANES 15 88% 1% 7
5 MITSUNOBU REACTION 9 13% 10% 62
6 PHOSPHONIUM ANHYDRIDES 8 60% 1% 9
7 ALKOXYDIPHENYLPHOSPHINES 8 100% 1% 5
8 DI ISOPROPYL AZODICARBOXYLATE 6 80% 1% 4
9 AZODICARBOXYLATE 6 23% 4% 25
10 MITSUNOBU TYPE ALKYLATION 4 67% 1% 4

Journals

Reviews



Title Publ. year Cit. Active references % act. ref.
to same field
The mitsunobu reaction: Origin, mechanism, improvements, and applications 2007 120 77 57%
Recent advances in the Mitsunobu reaction: Modified reagents and the quest for chromatography-free separation 2004 141 117 50%
Progress in the Mitsunobu reaction. A review 1996 357 148 32%
A NEW TYPE OF OXIDATION-REDUCTION CONDENSATION BY THE COMBINED USE OF PHENYL DIPHENYLPHOSPHINITE AND OXIDANT 2010 8 53 66%
Mitsunobu and Related Reactions: Advances and Applications 2009 384 1542 13%
Alkyl phosphinites: Versatile synthetic intermediates for dehydration condensation reactions 2007 7 15 87%
A general procedure for mitsunobu inversion of sterically hindered alcohols: Inversion of menthol. (1S,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl 4-nitrobenzoate - (Cyclohexanol, 5-methyl-2-(1-methylethyl)-, 4-nitrobenzoate, [1S-(1 alpha,2 alpha,5 beta]-) 1996 17 4 100%
Efficient method for the preparation of carboxylic acid alkyl esters or alkyl phenyl ethers by a new-type of oxidation-reduction condensation using 2,6-dimethyl-1,4-benzoquinone and alkoxydiphenylphosphines 2003 27 66 24%
Mitsunobu reaction of unbiased cyclic allylic alcohols 1997 37 70 31%
Development of new synthetic reagents in Mitsunobu-type reaction 2001 8 68 43%

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 DIRECT RECH SNC 1 50% 0.2% 1
2 DRUG SUBSTANCE DEV 1 50% 0.2% 1
3 EA3471 1 50% 0.2% 1
4 IWAKUNI PHARMACEUT TORY 1 50% 0.2% 1
5 KU CHEM METHODOL 1 50% 0.2% 1
6 OTIS A MARGARET T BARNES SCI 1 50% 0.2% 1
7 BIOORGAN CHEM ISOTOP ELING 0 33% 0.2% 1
8 LIB DEV EXCELLENCE 0 33% 0.2% 1
9 REACT SUBST SYST 11 2 0 33% 0.2% 1
10 AMINOACIDES PEPTIDES PROTEINES 0 25% 0.2% 1

Related classes at same level (level 1)



Rank Relatedness score Related classes
1 0.0000133746 AZAPEPTIDE//AZAPEPTIDES//AZA PEPTIDES
2 0.0000112086 AMIPRILOSE//SATURATED ALCOHOL//BENZYL PHENYL KETONE
3 0.0000107384 COMBINATORIAL PARALLEL MED CHEM//POLYMERIC OXIDIZING AGENT//GLAXOSMITHKLINE CAMBRIDGE TECHNOL
4 0.0000072266 NEW DRUG EACH DEV//HIGHER CARBON SUGARS//EPOXYSACCHARIDES
5 0.0000070526 OCTALACTIN//2 METHYL 6 NITROBENZOIC ANHYDRIDE//ACETIC ANHYDRIDE
6 0.0000068467 VARNISH REMOVAL//NUCLEOPHILE ASSISTING LEAVING GROUPS//ANORGAN BIOCHEM PHYSIOL CHEM
7 0.0000064951 BENZO1//CYCLIC TRITHIOCARBONATES//OXATHIINS
8 0.0000064210 2 3 DICHLORO 5 6 DICYANOBENZOQUINONE DDQ//PEPTIDE SYNTHESIS IN WATER//TRIPHENYLPHOSPHINE TPP
9 0.0000061557 ALKENYL NONAFLATES//CLAUSENAMIDE//CLAUSENAMIDE ENANTIOMERS
10 0.0000060157 CARBOCYCLIC NUCLEOSIDES//S ADENOSYLHOMOCYSTEINE HYDROLASE//CARBOCYCLIC NUCLEOSIDE