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Volumn 85, Issue 6, 2002, Pages 1827-1840

On rearrangements by cyclialkylations of arylpentanols to 2,3-dihydro-1H-indene derivatives. Part 1. An unexpected rearrangement by the acid-catalyzed cyclialkylation of 4-(2-chlorophenyl)-2,4-dimethyl pentan-2-ol under formation of trans-4-chloro-2,3-dihydro-1,1,2,3-tetramethyl-1H-indene;Über umlagerungen bei der cyclialkylierung von arylpentanolen zu 2,3-dihydro-1H-inden-derivaten 1. Mitteilung. Die säurekatalysierte, unter umlagerung verlaufende cyclialkylierung von 4-(chlorophenyl)-2,4-dimethylpentan-2-ol

(4) Blum, Roger a Giovannini, Edgardo a Hengartner, Urs a Vallat, Gabriel a

a UNIVERSITY OF FRIBOURG (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ACIDS; ALKYLATION; CATALYSIS; DERIVATIVES; MIXTURES;

CYCLIALKYLATION;

ALCOHOLS;

4 (2 CHLOROPHENYL) 2,4 DIMETHYLPENTAN 2 OL; 4 CHLORO 2,3 DIHYDRO 1,1,2,3 TETRAMETHYL 1H INDENE; CHLORIDE; INDENE DERIVATIVE; PENTANOL; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CATALYSIS; CHEMICAL REACTION; CYCLIZATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS;

EID: 0036295752 PISSN: 0018019X EISSN: None Source Type: Journal
DOI: 10.1002/1522-2675(200206)85:6<1827::AID-HLCA1827>3.0.CO;2-J Document Type: Article

Times cited : (11)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.