949463-53-0Relevant articles and documents
Formal synthesis of schulzeines B and C
Kuntiyong, Punlop,Akkarasamiyo, Sunisa,Piboonsrinakara, Nuanpan,Hemmara, Chitlada,Songthammawat, Poramate
, p. 8034 - 8040 (2011/11/06)
A formal synthesis of schulzeines B and C, marine natural products with inhibitory effect against α-glucosidase, has been achieved. The key reactions of the synthesis are N-acyliminium ion cyclization, Sharpless asymmetric dihydroxylation, olefin cross me
A new approach to the C28 fatty acid chain of the marine natural products schulzeines B and C: A concise diastereoselective total synthesis of(-)-schulzeine B
Yang, Chao,Bao, Yu-Hui,Liang, Pan,Ye, Jian-Liang,Wang, Ai-E.,Huang, Pei-Qiang
experimental part, p. 6281 - 6288 (2011/09/19)
An enantioselective approach to the C28 fatty acid chain of the marine natural products schulzeines B and C was established based on the l-tartaric acid derived C4 chiron 11 via successive 1,4-bis-chain elongation reactions and catal
Enantioselective synthesis of schulzeines B and C via a β-lactone-derived surrogate for bishomoserine aldehyde
Liu, Gang,Romo, Daniel
supporting information; experimental part, p. 1143 - 1146 (2009/07/25)
Enantioselective syntheses of the glucosidase inhibitors schulzeines B and C were achieved by employing a Pictet-Spengler reaction of a β-lactone-derived, masked bishomoserine aldehyde. Subsequent Corey-Link reaction unveiled an α-azido acid enabling cycl
Total syntheses of schulzeines B and C
Gurjar, Mukund K.,Pramanik, Chinmoy,Bhattasali, Debabrata,Ramana,Mohapatra, Debendra K.
, p. 6591 - 6594 (2008/02/10)
(Chemical Equation Presented) Schulzeines B (2) and C (3) were synthesized by a convergent strategy using epimeric tricyclic lactam building blocks, 4 and 5, and the C28 fatty acid side chain 6. Syntheses of tricyclic lactams (4/5) were achieved by Bischl