Organocatalytic enantioselective synthesis of alpha-hydroxy phosphonates.J Am Chem Soc. 2006 Jun 14; 128(23):7442-3.JA
Abstract
Tertiary alpha-hydroxy phosphonates have been synthesized in good yields and high enantiomeric purity (up to 99% ee) through a novel l-proline-catalyzed cross aldol reaction of alpha-keto phosphonates and ketones.
Links
Pub Type(s)
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
16756289
Citation
Samanta, Sampak, and Cong-Gui Zhao. "Organocatalytic Enantioselective Synthesis of Alpha-hydroxy Phosphonates." Journal of the American Chemical Society, vol. 128, no. 23, 2006, pp. 7442-3.
Samanta S, Zhao CG. Organocatalytic enantioselective synthesis of alpha-hydroxy phosphonates. J Am Chem Soc. 2006;128(23):7442-3.
Samanta, S., & Zhao, C. G. (2006). Organocatalytic enantioselective synthesis of alpha-hydroxy phosphonates. Journal of the American Chemical Society, 128(23), 7442-3.
Samanta S, Zhao CG. Organocatalytic Enantioselective Synthesis of Alpha-hydroxy Phosphonates. J Am Chem Soc. 2006 Jun 14;128(23):7442-3. PubMed PMID: 16756289.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Organocatalytic enantioselective synthesis of alpha-hydroxy phosphonates.
AU - Samanta,Sampak,
AU - Zhao,Cong-Gui,
PY - 2006/6/8/pubmed
PY - 2007/9/11/medline
PY - 2006/6/8/entrez
SP - 7442
EP - 3
JF - Journal of the American Chemical Society
JO - J Am Chem Soc
VL - 128
IS - 23
N2 - Tertiary alpha-hydroxy phosphonates have been synthesized in good yields and high enantiomeric purity (up to 99% ee) through a novel l-proline-catalyzed cross aldol reaction of alpha-keto phosphonates and ketones.
SN - 0002-7863
UR - https://www.unboundmedicine.com/medline/citation/16756289/Organocatalytic_enantioselective_synthesis_of_alpha_hydroxy_phosphonates_
DB - PRIME
DP - Unbound Medicine
ER -
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