82719-54-8Relevant articles and documents
Variation in the aromatic ring of cromakalim: Antihypertensive activity of pyranopyridines and 6-alkyl-2H-1-benzopyrans
Burrell,Cassidy,Evans,Lightowler,Stemp
, p. 3023 - 3027 (1990)
The synthesis and antihypertensive activity in the spontaneously hypertensive rat of two new series of analogues related to cromakalim (1) are described. In the first series, where the benzopyran nucleus has been replaced by a pyranopyridine nucleus, the
Benzopyran derivatives and processes for preparation thereof
-
, (2008/06/13)
Benzopyrene derivatives effective for the treatment of hypertension have been prepared.
A FACILE SYNTHESIS OF ARYL ETHERS OF ETHYNYLCARBINOLS USING THE MITSUNOBU REACTION
Subramanian, R. Sankara,Balasubramanian, K. K.
, p. 1255 - 1260 (2007/10/02)
The facile synthesis of a few aryl ethers of ethynylcarbinols using the Mitsunobu reaction is reported.
THERMAL AND CATALYTIC REARRANGEMENTS OF 4-(1,1-DIMETHYL-2-PROPENOXY)TOLUENE
Aleksandrova, E. K.,Bunina-Krivorukova, L. I.
, p. 742 - 745 (2007/10/02)
During the thermal and catalytic rearrangements of 4-(1,1-dimethyl-2-propenoxy)toluene the Claisen phenol, with inversion of the allyl unit, i.e., 4-methyl-2-(3-methyl-2-butenyl)phenol, is formed primarily.The formation of 2-methyl-2-(3-methyl-2-butenyl)phenol in the catalytic rearrangement with the introduction of o-cresol into the reaction zone shows that this rearrangement has partly intermolecular character.Consequently, the Claisen phenol can also be obtained by an intermolecular path, where this phenol is the most thermodynamically stable isomer.