Abstract
In the presence of a protonated cinchonine derivative, radical addition reactions proceeded efficiently, affording addition adducts in high yields with an extremely high enantioselectivity. The chiral ammonium salt was recyclable after a simple aqueous workup. The reaction provides environmentally benign reaction conditions.
| Original language | English |
|---|---|
| Pages (from-to) | 16152-16153 |
| Number of pages | 2 |
| Journal | Journal of the American Chemical Society |
| Volume | 130 |
| Issue number | 48 |
| DOIs | |
| Publication status | Published - 2008 Dec 3 |
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All Science Journal Classification (ASJC) codes
- Catalysis
- Chemistry(all)
- Biochemistry
- Colloid and Surface Chemistry
Cite this
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Highly enantioselective radical addition to N-benzoyl hydrazones using chiral ammonium salts. / Doo, Ok Jang; Sang, Yoon Kim.
In: Journal of the American Chemical Society, Vol. 130, No. 48, 03.12.2008, p. 16152-16153.Research output: Contribution to journal › Article
TY - JOUR
T1 - Highly enantioselective radical addition to N-benzoyl hydrazones using chiral ammonium salts
AU - Doo, Ok Jang
AU - Sang, Yoon Kim
PY - 2008/12/3
Y1 - 2008/12/3
N2 - In the presence of a protonated cinchonine derivative, radical addition reactions proceeded efficiently, affording addition adducts in high yields with an extremely high enantioselectivity. The chiral ammonium salt was recyclable after a simple aqueous workup. The reaction provides environmentally benign reaction conditions.
AB - In the presence of a protonated cinchonine derivative, radical addition reactions proceeded efficiently, affording addition adducts in high yields with an extremely high enantioselectivity. The chiral ammonium salt was recyclable after a simple aqueous workup. The reaction provides environmentally benign reaction conditions.
UR - http://www.scopus.com/inward/record.url?scp=57149109137&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=57149109137&partnerID=8YFLogxK
U2 - 10.1021/ja807685r
DO - 10.1021/ja807685r
M3 - Article
VL - 130
SP - 16152
EP - 16153
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 48
ER -