## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Conformational Switching and the Synthesis of Spiro[2 H -indol]-3(1 H )-ones by Radical Cyclization
✍ Scribed by Sulsky, Richard; Gougoutas, Jack Z.; DiMarco, John; Biller, Scott A.
- Book ID
- 125509698
- Publisher
- American Chemical Society
- Year
- 1999
- Tongue
- English
- Weight
- 184 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0022-3263
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract magnified image In a one‐pot procedure, the 3‐phenacylideneoxindoles **1a**, **1b**, **1c**, **1d** were reacted with hydrazine and then __in situ__ with lead(IV) acetate and new diastereoisomers of spiro[cyclopropane‐1,3′‐[3__H__]indol]‐2′(1′__H__)‐ones were prepared. Compounds **1a**,
## Abstract The molecular structures of two byproducts 1,1″‐diphenyl‐3′,4′‐dihydrodispiro[indole‐2,2′‐furan‐5′,2″‐indole]‐3,3″(1__H__, 1″__H__)‐dione (3) and 1,5′‐diphenyl‐4′,5′‐dihydro‐3′__H__‐spiro[indole‐2,2′‐pyrano[3,2‐__b__]indol]‐3(1__H__)‐one (4), which accompanied the rearrangement of 3‐hyd