o m b a y 4 0 0 076, India The conjugative ability of a spirocyclopropane on 4-en-$one steroids was studied with the help of I3C NMR and two-dimensional experiments such as COSY and NOESY. The conformational analysis of the A ring of these compounds indicates a 'normal' (la,ZB)-half-chair conformati
✦ LIBER ✦
A simple high-yielding synthesis of spiro[cyclopropane-1,2′-steroids]
✍ Scribed by Desai, Umesh R. ;Trivedi, Girish K.
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 173 KB
- Volume
- 1990
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
A high‐yielding synthesis of biologically active spiro‐[cyclopropane‐1,2′‐steroids] with a Δ^4^′‐3′‐one moiety by using the Simmons Smith reaction is described. 2‐Methylene‐4‐en‐3‐one steroids are treated with methylene iodide (ratio 1:1).
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