Record 1 of 9 Author(s) : Narasimhan S; Madhavan S; Prasad KG Title : A simple alkene-catalyzed reduction of aromatic esters to alcohols by zinc borohydride Source : SYNTHETIC COMMUNICATIONS 1997, Vol 27, Iss 3, pp 385-390 Publisher : MARCEL DEKKER INC Abstract : Reactivity of Zn(BH4)(2) was modified by adding cyclohexene to achieve the reduction of aromatic esters to alcohols which reaction was not possible previously because of the mild nature of the reagent. Functional groups like Cl and nitro were tolerated. Publisher address : 270 MADISON AVE, NEW YORK, NY 10016 ---------------------------------------------------------------------------- Record 2 of 9 Author(s) : Narasimhan S; Madhavan S; Balakumar R; Swarnalakshmi S Title : Unusual reactivity of zinc borohydride - Reduction of amides to amines Source : SYNTHETIC COMMUNICATIONS 1997, Vol 27, Iss 3, pp 391-394 Publisher : MARCEL DEKKER INC Abstract : Zinc borohydride reduces secondary amides to the corresponding N-ethyl amines in excellent yields. The reduction requires only stoichiometric quantities of hydride and does not require the addition of any Lewis acid. The amides are isolated by simple hydrolysis of the reaction mixture. Publisher address : 270 MADISON AVE, NEW YORK, NY 10016 ---------------------------------------------------------------------------- Record 3 of 9 Author(s) : Narasimhan S; Madhavan S; Prasad KG Title : Unusual reactivity of zinc borohydride - Conversion of amino acids to amino alcohols Source : SYNTHETIC COMMUNICATIONS 1996, Vol 26, Iss 4, pp 703-706 Publisher : MARCEL DEKKER INC Abstract : Zinc borohydride reduces amino acids with only stoichiometric amounts of hydride to the corresponding chiral alcohols in excellent yields in the absence of any Lewis acid. Publisher address : 270 MADISON AVE, NEW YORK, NY 10016 ---------------------------------------------------------------------------- Record 4 of 9 Author(s) : Narasimhan S; Prasad KG; Madhavan S Title : Synthesis of (3Z,13Z)-3,13-octadecadienyl acetate - Sex pheromone of synanthedon tenuis- using readily available C-11-synthon Source : INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY Publisher : COUNCIL SCIENTIFIC INDUSTRIAL RESEARCH Abstract : Synthesis of (3Z,13Z)-3,13-octadecadienyl acetate has been achieved from the readily available 10-undecen-1-ol using cheaper reagents and less number of steps. In the key step alkylation of an alkyne is performed with solid sodamide giving the product in 50% yield. The method can be easily scaled-up. Publisher address : PUBL & INFO DIRECTORATE, NEW DELHI 110012, INDIA ---------------------------------------------------------------------------- Record 5 of 9 Author(s) : NARASIMHAN S; MOHAN H; MADHAVAN S Title : ONE-CARBON HOMOLOGATION OF 10-UNDECENYL DERIVATIVES THROUGH PEROXIDE-CATALYZED ADDITION OF CARBON-TETRACHLORIDE Source : INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY Publisher : COUNCIL SCIENTIFIC INDUSTRIAL RESEARCH Abstract : A simple and convenient method to prepare the carbon tetrachloride adducts of various 10-undecenyl derivatives has been reported. Publisher address : PUBL & INFO DIRECTORATE, NEW DELHI 110012, INDIA ---------------------------------------------------------------------------- Record 6 of 9 Author(s) : NARASIMHAN S; MADHAVAN S; PRASAD KG Title : FACILE REDUCTION OF CARBOXYLIC-ACIDS BY ZINC BOROHYDRIDE Source : JOURNAL OF ORGANIC CHEMISTRY 1995, Vol 60, Iss 16, pp 5314-5315 Publisher : AMER CHEMICAL SOC Publisher address : PO BOX 57136, WASHINGTON, DC 20037-0136 ---------------------------------------------------------------------------- Record 7 of 9 Author(s) : NARASIMHAN S; MOHAN H; MADHAVAN S Title : A SIMPLE, COST-EFFECTIVE SYNTHESIS OF E,Z-2,13-OCTADECADIENYL ACETATE, A MAJOR SEX-PHEROMONE COMPONENT OF LEPIDOPTERAN PESTS Source : INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY Publisher : COUNCIL SCIENTIFIC INDUSTRIAL RESEARCH Abstract : A simple, cost effective synthesis of E,Z-2,13-octadecadienyl acetate (1), a major sex pheromone component of many lepidopteran pests, has been achieved in optimum number of steps using cheaper raw materials. The strategy provides the target compound in 43% overall yield, and can be scaled up easily. Publisher address : PUBL & INFO DIRECTORATE, NEW DELHI 110012, INDIA ---------------------------------------------------------------------------- Record 8 of 9 Author(s) : NARASIMHAN S; PRASAD KG; MADHAVAN S Title : CALCIUM BOROHYDRIDE - A REAGENT FOR FACILE CONVERSION OF CARBOXYLIC ESTERS TO ALCOHOLS AND ALDEHYDES Source : SYNTHETIC COMMUNICATIONS 1995, Vol 25, Iss 11, pp 1689-1697 Publisher : MARCEL DEKKER INC Abstract : Calcium borohydride reduces both aliphatic and aromatic esters to alcohols completely in the presence of alkene catalysts. The intermediate borates formed during the reduction of aromatic esters are converted to aldehydes with aqueous NaOCl in good yields. Publisher address : 270 MADISON AVE, NEW YORK, NY 10016 ---------------------------------------------------------------------------- Record 9 of 9 Author(s) : NARASIMHAN S; PRASAD KG; MADHAVAN S Title : REMARKABLE REGIOSELECTIVE HYDROBORATION OF TERMINAL ALKENES BY CALCIUM BOROHYDRIDE Source : TETRAHEDRON LETTERS 1995, Vol 36, Iss 7, pp 1141-1144 Publisher : PERGAMON-ELSEVIER SCIENCE LTD Abstract : Calcium borohydride is found to hydroborate unsaturated systems in the presence of ethyl acetate. The reaction exhibits remarkable selectivity towards terminal double bonds. Several Z-11-alken-1-ol pheromones are synthesized using this method. Publisher address : THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD, ENGLAND OX5 1GB ----------------------------------------------------------------------------