SCOPUS 정보 검색 플랫폼

Tetrahedron

Volumn 69, Issue 8, 2013, Pages 1994-2003

Baylis-Hillman acetates in carbocyclic synthesis: A convenient protocol for synthesis of densely substituted indenes

(3) Basavaiah, Deevi a Reddy, Bhavanam Sekhara a Lingam, Harathi a

a UNIVERSITY OF HYDERABAD (India)

Author keywords

Baylis Hillman reaction; Chemo selectivity; Friedel Crafts reaction; Indene derivatives; Keto diesters

Indexed keywords

1,4 DIAZABICYCLO[2.2.2]OCTANE; ACETIC ACID; CARBOXYLIC ACID; ESTER DERIVATIVE; ETHYL 1 (1 ETHOXYCARBONYLETHENYL) 3 METHYL 4,5,6 TRIMETHOXY 1H INDENE 2 CARBOXYLATE; ETHYL 1 (1 METHOXYCARBONYLETHENYL) 3 METHYL 4,5,6 METHOXY 1H INDENE 2 CARBOXYLATE; ETHYL 4,6 DIMETHOXY 1 (1 ETHOXYCARBONYLETHENYL) 3 METHYL 1H INDENE 2 CARBOXYLATE; ETHYL 4,6 DIMETHOXY 1 (1 METHOXYCARBONYLETHENYL) 3 METHYL 1H INDENE 2 CARBOXYLATE; INDENE DERIVATIVE; METHYL 1 (1 ETHOXYCARBONYLETHENYL) 3 METHYL 4,5,6 TRIMETHOXY 1H INDENE 2 CARBOXYLATE; METHYL 1 (1 METHOXYCARBONYLETHENYL) 3 METHYL 4,5,6 TRIMETHOXY 1H INDENE 2 CARBOXYLATE; METHYL 4,6 DIMETHOXY 1 (1 ETHOXYCARBONYLETHENYL) 3 METHYL 1H INDENE 2 CARBOXYLATE; METHYL 4,6 DIMETHOXY 1 (1 METHOXYCARBONYLETHENYL) 3 METHYL 1H INDENE 2 CARBOXYLATE; POTASSIUM CARBONATE; TITANIUM TETRACHLORIDE; UNCLASSIFIED DRUG;

ARTICLE; BAYLIS HILLMAN REACTION; CYCLIZATION; DRUG SYNTHESIS; FRIEDEL CRAFTS REACTION; MOLECULAR INTERACTION; NUCLEOPHILICITY; PRIORITY JOURNAL;

EID: 84873096967 PISSN: 00404020 EISSN: 14645416 Source Type: Journal
DOI: 10.1016/j.tet.2012.12.069 Document Type: Article

Times cited : (11)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.