Electrophile-induced domino cyclization reaction for the synthesis of 2,2a,10,11-tetrahydrofuro[2′,4′:4,6]pyrano[2,3-b]quinolines
✍ Scribed by Bhawana Singh; Atish Chandra; Shraddha Upadhyay; Radhey M. Singh; M.C. Puerta; Pedro Valerga
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 211 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The molecule of the title compound, C~26~H~30~N~2~O~4~S, adopts a folded conformation, with the sulfonyl-bound benzene ring lying over the pyridinone ring [centroid-to-centroid distance = 3.893 (1) Å], forming a dihedral angle of 23.87 (5)°. The pyrrolidine ring adopts a twist conformation and the d
The asymmetric unit of the title compound, C 26 H 30 N 2 O 4 S, consists of two independent molecules, A and B, with similar conformations. In both molecules, the pyrrolidine and dihydropyran rings adopt envelope conformations, and are trans-fused; the tosyl group is attached to the pyrrolidine ring
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v