Efficient Synthesis of 1‐(5′‐Acylamino‐1′,3′,4′‐thiadiazol‐2′‐yl)‐4‐acyl‐thiosemicarbazides

By Li Zheng   Yang Jing   Wang Xi  

Synthetic Communications, Vol. 36, Iss. 16, 2006-08 ,pp. : 2355-2362

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Rapid Access for the Synthesis of 1‐N‐Methyl‐spiro[2.3′]oxindole‐spiro[3.7″] (3″‐Aryl)‐5″‐methyl‐3″,3a″,4″,5″,6″,7″‐hexahydro‐2H‐pyrazolo[4,3‐ c ]pyridine‐4‐aryl‐pyrrolidines Through Sequential 1,3‐Dipolar Cycloaddition and Annulation

By Sridhar Gowri   Raghunathan R.  

Synthetic Communications, Vol. 36, Iss. 1, 2006-02 ,pp. : 21-29

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Asymmetric Synthesis of (2S)‐1‐(3,4‐Dihydroxyphenoxy)‐3‐(3,′4′‐Dimethoxyphenoxy) Ethylamino‐2‐propanol hydrochloride (RO363)

By Narsaiah Akkirala  

Synthetic Communications, Vol. 36, Iss. 13, 2006-07 ,pp. : 1897-1901

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One‐Pot Resolution of trans ‐2‐Iodo‐cyclohexanol with O , O ′‐Dibenzoyl‐(2 R ,3 R )‐tartaric Acid in Solid Phase

By Kassai C.   Fogassy E.   Kozma D.  

Synthetic Communications, Vol. 36, Iss. 8, 2006-05 ,pp. : 1015-1018

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Synthesis of Potentially Bioactive Heterocycles: Thermal [3,3]Sigmatropic Rearrangement of 4‐(4′‐Aryloxybut‐2′‐ynyloxy)‐6‐methyl‐2‐pyridone

By Majumdar K.   Rahaman H.   Roy B.  

Synthetic Communications, Vol. 36, Iss. 6, 2006-04 ,pp. : 809-816

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