## Abstract The syntheses of 5α‐ and 5β‐cholest‐3‐eno[4,3‐__d__]pyrimidines (7) and (7′) could be achieved by using the hydroxymethylene derivative of cholestan‐4‐one (5) prepared from cholesterol (1). Their 2′‐derivatives 7a‐7d and 7′a‐7′c were also synthesized. 5α‐Cholest‐6‐eno[7,6‐__d__]pyrimidi
Syntheses and CD studies of 5α-cholesteno[3,2-d]-, -[2,3-d]- and -[3,4-d]pyrimidines
✍ Scribed by Hasan, Mashooda ;Rashid, Naghmana ;Khan, Khalid Mohammed ;Snatzke, Günther ;Duddeck, Helmut ;Voelter, Wolfgang
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 857 KB
- Volume
- 1995
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
and [3,4-d]
pyrimidines (15a) have been achieved by using hydroxymethylene derivatives of relevant cholestanones prepared from cholesterol (1). Their CD spectra exhibit at least three Cotton effects between 300 to 200 nm, a first CD band around 290, a second one around 260 and a third one around 220 nm. A quadrant rule is developed and applied to the determination of the sign of the first CD band, while a helicity rule is applicable to the third CD band. The first band is positive in the [3,2-d] series, whereas it is negative in the [2,3d ] and the [3,4-d] series. The third band is negative in all three series.
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## Abstract Diethyl 2‐[(ethoxythioxomethyl)amino]‐4,5,6,7‐tetrahydrothieno[2,3‐c]‐pyridine‐3,6‐dicarboxylate **2**, prepared from diethyl 2‐isothiocyanato‐4,5,6,7‐tetrahydrothieno[2,3‐c]pyridine‐3,6‐dicarboxylate **1** by boiling in anhydrous ethanol, was converted into pyrido[4′,3′:4,5]thieno[2,3‐
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