TY  - JOUR 
AU  - Sedano Labrador, Carlos
AU  - Virumbrales Ortiz, Cintia
AU  - Suarez Pantiga, Samuel
AU  - Sanz Díez, Roberto
PY  - 2021
SN  - 0039-7881
UR  - http://hdl.handle.net/10259/6089
AB  - α-Oxy ketones, easily accessible by conventional routes, can be selectively deprotonated generating an enolate intermediate, which upon treatment with paraformaldehyde undergoes an aldol–Tishchenko reaction, leading to relevant 1,2,3-triol fragments...
LA  - eng
PB  - Thieme
KW  - aldol–Tishchenko reaction
KW  - enolates
KW  - α-oxy ketones
KW  - polyol derivatives
KW  - diastereoselectivity
KW  - oxetanes
KW  - Química orgánica
KW  - Chemistry, Organic
TI  - Aldol–Tishchenko Reaction of α-Oxy Ketones: Diastereoselective Synthesis of 1,2,3-Triol Derivatives
DO  - 10.1055/a-1509-5655
ER  -