Premium
Ester and Lactone Formation with the Reagent 1,2‐Dihydro‐4,6‐dimethyl‐2‐thioxo‐3‐pyridinecarbonitrile
Author(s) -
Schmidt Ulrich,
Heermann Dieter
Publication year - 1979
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.197903082
Subject(s) - lactone , reagent , chemistry , organic chemistry , combinatorial chemistry
Transformation of long‐chain ω‐hydroxy acids into the macrolactone can be accomplished with the title compound. The disulfied derived therefrom is esterified with the acid to give (1) ; on heating (1) gives the lactone. The thiol esters (1) are less expensive and more readily accessible than comparably reactive lactone precursors.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom