The mechanism of the Mitsunobu azide modification and the effect of additives on the rate of hydroxyl group activation.

Tetrahedron

Volumn 50, Issue 32, 1994, Pages 9671-9678

  M Afonso, Carlos ^a   Teresa Barros, M ^a,b   S Godinho, Licio ^a   D Maycock, Christopher ^b,c  

^a UNIVERSIDADE NOVA DE LISBOA   (Portugal)

^b INSTITUTO DE TECNOLOGIA QUÍMICA E BIOLÓGICA   (Portugal)

^c UNIVERSITY OF LISBON   (Portugal)

Author keywords

[No Author keywords available]

Indexed keywords

ESTER;

ARTICLE; DRUG SYNTHESIS; ESTERIFICATION; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0028041388     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)85535-6     Document Type: Article

References (21)

1. Preparation of Esters of Phosphoric Acid by the Reaction of Trivalent Phosphorus Compounds with Diethyl Azodicarboxylate in the Presence of Alcohols
2. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
3. The Mechanism of the Mitsunobu Reaction. III. The Use of Tributylphosphine
4. The mechanism of the mitsunobu reaction and its application to CO2 fixation
5. Synthesis of the macrolactone pyrrolizidine alkaloid integerrimine
6. The Mechanism of the Mitsunobu Reaction. III. The Use of Tributylphosphine