Abstract
Benzotriazole surrogates showing higher stabilities than the corresponding chlorophosphates, allow phosphonylation of a variety of N-, O-, and S-nucleophiles in good yields.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 5898-5901 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 55 |
| Issue number | 43 |
| DOIs | |
| State | Published - Oct 22 2014 |
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Keywords
- Benzotriazole
- Conjugates
- Methodology
- Nucleophile
- Phosphonylation
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
New benzotriazole-based reagents for the phosphonylation of various N-, O-, and S-nucleophiles. / Panda, Siva S.; Steel, Peter J.
In: Tetrahedron Letters, Vol. 55, No. 43, 22.10.2014, p. 5898-5901.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - New benzotriazole-based reagents for the phosphonylation of various N-, O-, and S-nucleophiles
AU - Panda, Siva S.
AU - Steel, Peter J.
PY - 2014/10/22
Y1 - 2014/10/22
N2 - Benzotriazole surrogates showing higher stabilities than the corresponding chlorophosphates, allow phosphonylation of a variety of N-, O-, and S-nucleophiles in good yields.
AB - Benzotriazole surrogates showing higher stabilities than the corresponding chlorophosphates, allow phosphonylation of a variety of N-, O-, and S-nucleophiles in good yields.
KW - Benzotriazole
KW - Conjugates
KW - Methodology
KW - Nucleophile
KW - Phosphonylation
UR - http://www.scopus.com/inward/record.url?scp=84907452285&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84907452285&partnerID=8YFLogxK
U2 - 10.1016/j.tetlet.2014.07.057
DO - 10.1016/j.tetlet.2014.07.057
M3 - Article
AN - SCOPUS:84907452285
VL - 55
SP - 5898
EP - 5901
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 43
ER -