Hydroxyl-directed reduction of β-hydroxycycloalkanones as a stereoselective route to 1,3-diols: X-ray crystal structure and structural features of (1R*,2R*,6S*)-2-[hydroxy(phenyl)methyl]cyclopentanol-Reference-Cited by-同舟云学术

Hydroxyl-directed reduction of β-hydroxycycloalkanones as a stereoselective route to 1,3-diols: X-ray crystal structure and structural features of (1R*,2R*,6S*)-2-[hydroxy(phenyl)methyl]cyclopentanol

Published:1995 Issue:4 Volume: Page:379-383
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Thompson Stephen H. J.,Mahon Mary F.,Molloy Kieran C.,Hadley Michael S.,Gallagher Timothy

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1995/P1/P19950000379

Reference34 articles.

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2. M. Nórgrádi , Stereoselective Synthesis, VCH, New York, 1986, pp. 131–148;

3. An introduction of chiral centers into acyclic systems based on stereoselective ketone reduction

4. Chelation-controlled protocol for the diastereoselective reduction of ketones

5. Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride

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