Stereoselectivity in the photoinduced electron transfer (PET) promoted intramolecular cyclisations of 1-alkenyl-2-silyl-piperidines and -pyrrolidines: rapid construction of 1-azabicyclo[m.n.0]alkanes and stereoselective synthesis of (±)-isoretronecanol and (±)-epilupinine-Reference-Cited by-同舟云学术

Stereoselectivity in the photoinduced electron transfer (PET) promoted intramolecular cyclisations of 1-alkenyl-2-silyl-piperidines and -pyrrolidines: rapid construction of 1-azabicyclo[m.n.0]alkanes and stereoselective synthesis of (±)-isoretronecanol and (±)-epilupinine

Published:1996 Issue:2 Volume: Page:219-224
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Pandey Ganesh,Reddy Gottimukkula Devi,Chakrabarti Debasish

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1996/P1/P19960000219

Reference34 articles.

1. Photoinduced electron transfer (PET) promoted cyclisations of 1-[N-alkyl-N-(trimethylsilyl)methyl]amines tethered to proximate olefin: mechanistic and synthetic perspectives

2. Stereoselectivity in the cyclisation of photoinduced electron transfer (PET) generated cyclic (α -amino radicals: First general stereoselective entry to 1-azabicyclo (m:n:o) alkane systems

3. A. R. Pinder , in The Alkaloids, ed. M. F. Grundon, The Royal Society of Chemistry, London, 198212.

4. For reviews on pyrrolizidine alkaloids, see: R. V.Stevens, in The Total Synthesis of Natural Products, ed. J. Apsimon, Wiley, New York, 1977, vol. 3, p. 439;

5. Pyrrolizidine alkaloids

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