roflamycoin

roflamycoin 구조식 이미지
카스 번호:
77814-07-4
상품명:
roflamycoin
동의어(영문):
Roflamycoin;14,37-Dioxabicyclo[31.3.1]heptatriaconta-3,5,7,9,11-pentaen-13-one, 19,21,23,25,27,29,31,33,35-nonahydroxy-12,16-dimethyl-15-(1-methylethyl)-, (1R,3E,5E,7E,9E,11E,15S,16S,19S,21S,23S,25R,27R,29S,31R,33S,35S)- (9CI)
CBNumber:
CB88188494
분자식:
C40H66O12
포뮬러 무게:
738.94
MOL 파일:
77814-07-4.mol

roflamycoin 속성

끓는 점
972.8±65.0 °C(Predicted)
밀도
1.154±0.06 g/cm3(Predicted)
산도 계수 (pKa)
12.67±0.70(Predicted)

안전

roflamycoin C화학적 특성, 용도, 생산

Synthesis

For Rychnovsky and co-worker’s synthesis of roflamycoin (45), the hemiketal-pyran linkage required differential substitution (Scheme 9) and demonstrated the power of the sequential double addition strategy.14 Treatment of bis-epoxide S,S-4 with a stoichiometric amount of (benzyloxy)methyllithium 38 and BF3?OEt2 in THF at –78 °C provided monoaddition adduct 39, which was then treated with the organolithium formed from transmetallation of 2,2-bis-(tributyltin)dithiane 40. This single-pot procedure afforded dithiane diol 41 in 56% overall yield. Subsequent acetonide formation and transmetallation provided a competent nucleophile for direct displacement of dibromide 42, which itself was derived from dichlorodiol R,R-3. The resulting bis-acetonide (43) was obtained in 60% overall yield and provided a rapid access to tris-acetonide 44, a key intermediate for the synthesis of the hemiketal-pyran moiety of 45. Similar sequential addition strategies have proven to be useful as well.
roflamycoin synthesis

roflamycoin 준비 용품 및 원자재

원자재

준비 용품


roflamycoin 공급 업체

글로벌( 3)공급 업체
공급자 전화 이메일 국가 제품 수 이점
BOC Sciences
16314854226; +16314854226
inquiry@bocsci.com United States 19743 58
Zhejiang Huida Biotech Co., LTD 0571-89903882 13626641628
jiangnan@huidabiotech.com China 3657 58
Zhejiang Huida Biotech Co., LTD 0571-0571-89903882 15990081639
sunshixuan@huidabiotech.com China 3705 58

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