623936-74-3

Upstream product

• 623936-94-7 (2S,3R)-3-[(1S,2R)-2-((S)-3-Benzyloxy-2-tert-butoxycarbonylamino-propionyloxy)-1-methyl-pentadecyl]-oxirane-2-carboxylic acid allyl ester 
• 623936-96-9 (2S,3R)-3-[(1S,2R)-2-((S)-3-Benzyloxy-2-tert-butoxycarbonylamino-propionyloxy)-1-methyl-pentadecyl]-oxirane-2-carboxylic acid 
• 623936-89-0 (2S,3R)-3-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-pentadecyl]-oxirane-2-carboxylic acid allyl ester 
• 623936-81-2 {(2R,3R)-3-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-pentadecyl]-oxiranyl}-methanol 
• 623936-91-4 (2S,3R)-3-((1S,2R)-2-Hydroxy-1-methyl-pentadecyl)-oxirane-2-carboxylic acid allyl ester 
• 867039-02-9 (2S,3R)-3-((1S,2R)-2-{(S)-3-Benzyloxy-2-[(2S,3R)-3-benzyloxy-2-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-butyrylamino]-propionyloxy}-1-methyl-pentadecyl)-oxirane-2-carboxylic acid allyl ester 
• 623937-00-8 (2S,3R)-3-Benzyloxy-2-[(S)-2-({(2S,3R)-3-[(1S,2R)-2-((S)-3-benzyloxy-2-tert-butoxycarbonylamino-propionyloxy)-1-methyl-pentadecyl]-oxiranecarbonyl}-amino)-3-methyl-butyrylamino]-butyric acid allyl ester 
• 867039-03-0 (2S,3R)-3-((1S,2R)-2-{(S)-3-Benzyloxy-2-[(2S,3R)-3-benzyloxy-2-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-butyrylamino]-propionyloxy}-1-methyl-pentadecyl)-oxirane-2-carboxylic acid 
• 623937-02-0 (2S,3R)-3-Benzyloxy-2-[(S)-2-({(2S,3R)-3-[(1S,2R)-2-((S)-3-benzyloxy-2-tert-butoxycarbonylamino-propionyloxy)-1-methyl-pentadecyl]-oxiranecarbonyl}-amino)-3-methyl-butyrylamino]-butyric acid 
• 623936-85-6 (2S,3R)-3-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-pentadecyl]-oxirane-2-carboxylic acid 
• 623936-79-8 (E)-(4R,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-octadec-2-enoic acid methyl ester 
• 623936-80-1 (E)-(4R,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-octadec-2-en-1-ol 
• 452956-79-5 2,2-Dimethyl-propionic acid (2R,3R)-3-(tert-butyl-dimethyl-silanyloxy)-2-methyl-hexadecyl ester 
• 452956-80-8 (2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-methyl-hexadecan-1-ol 

Relevant academic research and scientific papers

Synthetic studies on stevastelins. 1. Total synthesis of stevastelins B and B3

The synthesis of stevastelin B3 (2) and B (5) are described. In a first approach, epoxy cyclodepsipeptide 8 was considered as a promising candidate for the synthesis of the [15]-membered ring members of the stevastelins; however, the oxirane ring opening,

Towards the synthesis of [15]-membered stevastelins through the 2,3-epoxy analogues

A synthetic approach to the [15]-membered stevastelins, a novel class of immunosuppressant agents, is reported based on a macrolactamization route to the 2,3-epoxy derivative 6. The synthesis of this compound was achieved via a stereoselective epoxidation