Results
1 -
5 of
5
(Click
here to explore results)
- Ru-catalyzed asymmetric hydrogenation of δ-keto Weinreb amides: enantioselective synthesis of (+)-Centrolobine. Mengmeng Zhao, Bin Lu, Guangni Ding, Kai Ren, Xiaomin Xie, Zhaoguo Zhang
, Org. Biomol. Chem.
, 2016
, 14
, 2723
- Enantioselective synthesis of δ-/γ-alkoxy-β-hydroxy-α-alkyl-substituted Weinreb amides
via DKR–ATH: application to the synthesis of advanced intermediate of (−)-brevisamide. Gullapalli Kumaraswamy, Akula Narayana Murthy, Vykunthapu Narayanarao, Sahithya Phani Babu Vemulapalli, Jagadeesh Bharatam
, Org. Biomol. Chem.
, 2013
, 11
, 6751
- Intermolecular CDC amination of remote and proximal unactivated Csp3
–H bonds through intrinsic substrate reactivity – expanding towards a traceless directing group. Suresh Rajamanickam, Mayank Saraswat, Sugumar Venkataramani, Bhisma K. Patel
, Chem. Sci.
, 2021
, 12
, 15318
- Approaches to the synthesis of (2R,3S)-2-hydroxymethylpyrrolidin-3-ol (CYB-3) and its C(3) epimer: a cautionary tale. Alison N. Hulme, Karen S. Curley
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 1083
- A flexible and efficient synthesis of the pyrrolidine α-glycosidase inhibitor
1,4-dideoxy-1,4-imino-D-arabinitol (DAB-1). Alison N. Hulme, Charles H. Montgomery, David K. Henderson
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 1837