Halo- and selenolactonisation: The two major strategies for cyclofunctionalisation

Tetrahedron

Volumn 60, Issue 25, 2004, Pages 5273-5308

  Ranganathan, Subramania ^a,b   Muraleedharan, K M ^a   Vaish, Narendra K ^a   Jayaraman, Narayanaswamy ^c  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

^b JAWAHARLAL NEHRU CENTRE FOR ADVANCED SCIENTIFIC RESEARCH   (India)

^c INDIAN INSTITUTE OF SCIENCE   (India)

Author keywords

Ac, Acetyl; Bn, Benzyl; Boc, tButoxycarbonyl; Carboxylic acid; Cbz, Benzyloxycarbonyl; Cp, Cyclopentadienyl; CSA, Camphorsulphonic acid; DCN, Dicyanonaphthalene; DME, Dimethoxyethane; Lactonisation; mCPBA, m Chloroperbenzoic acid; Stereoselectivity

Indexed keywords

ALKENE DERIVATIVE; ALLYL COMPOUND; AMIDE; CARBOXYLIC ACID DERIVATIVE; CYCLOPENTADIENE DERIVATIVE; ESTER; FATTY ACID; FUNCTIONAL GROUP; HYDROXYL GROUP; LACTONE DERIVATIVE; NITRILE; NORBORNENE DERIVATIVE; PHOSPHONIC ACID DERIVATIVE; PROSTANOID;

ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; CLAISEN REARRANGEMENT; COMPARATIVE STUDY; CONFORMATION; HALOLACTONISATION; KINETICS; MULTIPLE CHEMICAL SENSITIVITY; PRIORITY JOURNAL; SELENOLACTONISATION; STEREOCHEMISTRY; SYNTHESIS; THERMODYNAMICS;

EID: 2542478906     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.04.014     Document Type: Review

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