374900-92-2

Upstream product

• 374900-91-1 Triisopropyl-((R)-2-{(R)-5-[2-(4-methoxy-benzyloxy)-eth-(Z)-ylidene]-tetrahydro-pyran-2-yl}-3-phenylsulfanyl-propoxy)-silane 
• 374900-89-7 (R)-2-{(R)-5-[2-(4-Methoxy-benzyloxy)-eth-(Z)-ylidene]-tetrahydro-pyran-2-yl}-3-triisopropylsilanyloxy-propan-1-ol 
• 337971-14-9 (R)-(5'Z)-triisopropyl{2-[5'-[2''-(4'''-methoxybenzyloxy)ethylidene]tetrahydropyran-2'-yl]allyloxy}silane 

Downstream Products

• 374900-93-3 (S)-2-{(R)-5-[2-(4-Methoxy-benzyloxy)-eth-(Z)-ylidene]-tetrahydro-pyran-2-yl}-6-methyl-hept-5-enal 

Relevant academic research and scientific papers

Formal total synthesis of testudinariol A, a triterpene with C2 symmetry

The alcohol corresponding to half of the molecule of testudinariol A, a triterpene with a symmetric C2 structure isolated from Pleurobrancus testudinarius, was enantioselectively synthesized. The alcohol has been converted to testudinariol A by Mori et al.